Homeostatic capabilities of the choroid plexus epithelium in Alzheimer's disease

  • Conrad Johanson1Email author,

    Affiliated with

    • Paul McMillan2,

      Affiliated with

      • Rosemarie Tavares2,

        Affiliated with

        • Anthony Spangenberger1,

          Affiliated with

          • John Duncan1,

            Affiliated with

            • Gerald Silverberg1 and

              Affiliated with

              • Edward Stopa1, 2

                Affiliated with

                Cerebrospinal Fluid Research20041:3

                DOI: 10.1186/1743-8454-1-3

                Received: 21 November 2004

                Accepted: 10 December 2004

                Published: 10 December 2004


                As the secretory source of vitamins, peptides and hormones for neurons, the choroid plexus (CP) epithelium critically provides substances for brain homeostasis. This distributive process of cerebrospinal fluid (CSF) volume transmission reaches many cellular targets in the CNS. In ageing and ageing-related dementias, the CP-CSF system is less able to regulate brain interstitial fluid. CP primarily generates CSF bulk flow, and so its malfunctioning exacerbates Alzheimers disease (AD). Considerable attention has been devoted to the blood-brain barrier in AD, but more insight is needed on regulatory systems at the human blood-CSF barrier in order to improve epithelial function in severe disease. Using autopsied CP specimens from AD patients, we immunocytochemically examined expression of heat shock proteins (HSP90 and GRP94), fibroblast growth factor receptors (FGFr) and a fluid-regulatory protein (NaK2Cl cotransporter isoform 1 or NKCC1). CP upregulated HSP90, FGFr and NKCC1, even in end-stage AD. These CP adjustments involve growth factors and neuropeptides that help to buffer perturbations in CNS water balance and metabolism. They shed light on CP-CSF system responses to ventriculomegaly and the altered intracranial pressure that occurs in AD and normal pressure hydrocephalus. The ability of injured CP to express key regulatory proteins even at Braak stage V/VI, points to plasticity and function that may be boosted by drug treatment to expedite CSF dynamics. The enhanced expression of human CP 'homeostatic proteins' in AD dementia is discussed in relation to brain deficits and pharmacology.


                Choroid plexus impact on Alzheimer's disease

                Accumulating evidence supports the idea that continually decreasing choroid plexus (CP) function in advanced ageing exacerbates Alzheimer's disease (AD). As part of a new paradigm to explain brain interstitium deterioration in age-related dementias, increasingly more attention is being paid to the role of compromised blood-CSF [1] and blood-brain [2] barriers. Structural alterations and functional failures in CP as well as brain capillary transport systems adversely affect fluid dynamics and composition [3, 4]. This review treats mainly CP dysfunction and the compensatory reactions that occur in this epithelium in AD.

                Efficient CSF turnover is essential for a healthy brain. It depends upon an exquisite balance between CSF formation and reabsorption [5]. Compromised secretory phenomena at the CP 'upstream' predispose the brain to AD-type problems. On the other hand, defective clearance of CSF at the arachnoid membrane 'downstream' leads to normal pressure hydrocephalus (NPH) [6]. The pivotal role of the CP in CSF homeostasis and brain viability becomes more evident when the system fails. More information is needed to evaluate how diminishing choroidal functions affect the surrounding brain in the face of AD and other dementias.

                Brain fluid homeostasis: The role of CSF volume transmission

                In serving the brain's metabolic needs by supplying 'biochemical goods', the CP uses CSF as a conduit for convecting substances [7]. Numerous solutes ranging from ions to large proteins are entrained in the CSF that percolates through the ventricular axis (Fig. 1). CSF intimately contacts the periventricular brain tissue with which it exchanges materials bidirectionally by diffusion and bulk flow. Continually undergoing chemical modification as it flows downstream, the CSF completes the volume transmission process [7] by draining into venous blood at distal arachnoidal sites (Fig. 1).
                Figure 1

                Schema for CSF convection of water and solutes: Arterial blood perfusing the choroid plexus continually provides water, ions and organic substrates for the CP epithelial cells to form the CSF that underlies volume transmission. Manufactured by the CP epithelium as the result of numerous transport processes, the CSF is actively secreted into the ventricles. In transit through the ventricular cavities to the arachnoid drainage sites, the CSF exchanges anabolites and catabolites with brain interstitial fluid. As a result, trophic and signaling molecules are delivered (blue arrow) to the neurons and, concurrently, toxic waste products and unneeded proteins are removed (red arrow) by CSF 'sink action' on the brain. The permeable ependymal membrane allows bi-directional diffusion of beneficial and harmful molecules. Bulk flow or volume transmission of CSF is thus essential in effecting the homeostasis of fluid composition.

                Reduced formation of CSF and stagnated flow in ageing and AD [4] limits the delivery of substances to neurons. This debilitates brain function [3]. Numerous proteins are synthesized and secreted by CP into CSF. Other substances are transported from blood. Table 1 overviews molecules normally distributed by the CP-CSF nexus. Arginine vasopressin (AVP) is a neuropeptide synthesized by CP epithelium and secreted into CSF [8, 9]; it regulates CSF formation and modulates hippocampal memory mechanisms [10, 11]. Growth factors foster cell growth, blood supply and water balance [1]. Trace element distribution across CP is complex and involves many mechanisms. Iron transport into CSF, for example, is regulated by several proteins [1] alterations in which may predispose to amyloidogenesis [12]. Vitamins B and C are actively transported at the blood-CSF barrier [13]. This stabilizes their concentration in CSF, except in late-onset AD [14]. The net entry of nucleoside bases into CSF is also determined by active transporters in CP [15, 16]. Cysteine protease inhibitors like cystatin C are synthesized in CP epithelium for transport into CSF [17]. Hormones such as leptin and prolactin are translocated from plasma to CSF by saturable choroidal receptors [18, 19]. Overall it is striking that the CP-CSF interface engages in such prolific transport. Disease-associated interference with CP transporters and volume transmission limits the availability of CSF molecules for the brain [1, 20].
                Table 1

                Substances distributed to brain by transport at the blood-CSF gateway

                Class or group





                Arginine vasopressin

                Regulation of CSF formation


                Growth factors

                Basic fibroblast growth factor

                Integration of water balance

                [55, 104]

                Trace elements


                Enzyme function in neurons/glia

                [1, 12]


                Ascorbate & folate

                Antioxidants & co-factors for brain

                [13, 14]

                Nucleoside bases


                Nucleic acids & drug transport

                [15, 16]

                Protease inhibitors

                Cystatin C

                Neuroprotection after ischemia

                [1, 17]


                Prolactin & leptin

                Modulation of hypothalamus

                [18, 19]

                Structural and functional damage to the choroid plexus in AD

                Structure intimately relates to function in various epithelia. Therefore it is useful to analyze histopathological damage to CP at various stages of AD in order to clarify the onset of functional losses at the blood-CSF barrier. Ageing and AD cause similar degeneration in CP. Structural changes in AD though are usually greater than in non-demented control counterparts [21]. Serot and colleagues have delineated modifications in the choroidal epithelium, stroma and vessels in AD subjects [2224]. There are substantial alterations in all tissue compartments.

                Several features characterizing the CP in AD are highlighted in Table 2. Epithelial cells are typically truncated, with an average volume 70% of that at birth. Such epithelial atrophy likely affects cellular functions. Particularly prominent is an increase in the number of Biondi bodies in AD [25]. These bodies are fibrillar inclusions in the cytoplasm of very old epithelial cells. Lipofuchsin vacuoles also occur frequently in the cytoplasm. The basement membrane underlying the cell often thickens to 350 nm, compared to a much thinner membrane (ca. 100 nm) in neonates [21]. Another liability in AD is immunological deposition of C1q, IgG and IgM along the epithelial basement membrane. As fibrosis intensifies with age and disease, the stroma attains a thickness of a few tenths of a micron [21]. At the inner core of the choroidal villus, the blood vessel walls thicken. This coincides with the appearance of amyloid, hyaline bodies, psammomas and calcifications. Altogether, the histopathologic changes in CP compartments point to grossly-declining secretory functions in AD. Such structural abnormalities coincide with diminished CSF production in ageing [26] and AD patients [4].
                Table 2

                Pathological changes in choroid plexus in Alzheimer's diseasea

                Epithelial atrophy (↓ cell size by 1/3)

                ↑ Biondi bodies

                Lipofuchsin vacuoles

                Basement membrane thickening (3-fold ↑)

                ↑ Stromal fibrosis

                IgG and IgM depositions

                aDescribed by Serot and colleagues in refs. 22–24

                Due to the functional nexus of the CSF with brain interstitial fluid, the neuronal microenvironment in AD is impacted by markedly altered transport and permeability in CP. When neurodegenerative diseases, ischemia [27, 28] and elevated pressure [29, 30] inflict damage on the choroidal epithelium, there are resultant adverse changes in CSF composition and volume. Because neurons are sensitive to instabilities in CSF dynamics and constituents, it is important to assess the nature and progression of disrupted CP function in chronic diseases. In view of the expanding number of AD victims, it is timely to consider patterns of expression of chaperone proteins, receptors and transporters in CP at various Braak stages. Such information may abet future attempts to stabilize choroid plexus functional integrity perturbed in early AD dementia.

                Choroid plexus defense against insults in ageing and degeneration

                The CP is multifunctional, performing a wide range of homeostatic functions for the CNS [5]. CSF homeostasis is mediated mainly by CP. It involves the activity of many protein transporters and receptors at the basolateral and apical surfaces of the epithelial cells [31]. In addition to providing organic solutes for nutritive and trophic support of the brain, the CP secretions into the ventricles adjust the pH, osmolality, [K+] and immune molecule content of the CNS extracellular fluid [7]. Accordingly, healthy neurons are fundamentally dependent upon transport at the blood-CSF and blood-brain interfaces.

                Moreover to provide steady neuroprotection by regulating the extracellular milieu, the CP must protect itself against various stressor agents that build up during ageing and disease. There have been few investigations of the homeostatic systems within CP that stabilize choroidal functions in the face of ageing and AD. We have explored some candidate systems for compensatory responses by CP. Cytoplasmic heat shock proteins chaperone and perform housekeeping to maintain a healthy steady-state intraepithelial milieu [1, 32]. Growth factors critically minimize cell morbidity and mortality [27]. Fluid-regulating proteins correct ion and water imbalances that occur in neurodegenerative diseases. Consequently our hypothesis is that the upregulation of certain proteins in CP (such as those discussed above) thwarts certain untoward effects of ageing and disease progression. The protein expression aspect of the hypothesis was tested by analyzing immunostaining patterns in human CP specimens from patients with varying severity of AD.

                Analyses of human choroid plexus: Usefulness and challenges

                It is difficult to functionally assess the CP in vivo [30, 33], particularly in man. Alternatively one can evaluate the status of human CP in disease by analyzing autopsied tissues for variable protein expression [34]. Such findings are compared to appropriate age-matched controls. Immumocytochemical and biochemical data gleaned from human CP highlight directions to pursue with living animal models: transgenic mice with an AD phenotype or aged rats with CSF pathophysiology. Because protein expression relates to disease progression, it is essential to standardize grading for the severity of AD in subjects. We use a modified Braak & Braak staging system [35]: stages I/II (mild; disease involves hippocampus and entorhinal cortex); stages III/IV (moderate; AD spreading to the rest of the limbic lobe, e.g., amygdala); and stages V/VI (severe; further AD spreading to the prefrontal neocortex).

                Information about functional proteins in human CP is scarce. However protein expression was recently analyzed in autopsied lateral ventricle CP from normal adult brains and in those with confirmed AD [36, 37]. The ages investigated were generally between 65 and 90 yr for all subjects. Control individuals typically died from cardiac disease or tumors. AD specimens covered all Braak stages. Causes of the AD deaths were usually cardiac complications or pneumonia [37]. Fortunately the postmortem intervals (mainly between 2 and 18 hr) did not affect antibody staining [37]. For specimen quality it is desirable to procure choroidal tissues quickly after death. Human CP banks are needed to systematically catalog tissues from various stages of AD.

                Regulation of CP 'homeostatic proteins' in health and disease

                Ageing and AD dementia tax the CP and other CNS transport interfaces. In late life the deteriorating brain presents many potentially-destructive metabolites to the CSF for multi-site excretion into blood. The greater burden of macromolecule disposal in AD occurs when CP and arachnoid membrane, due to ageing debilities, are less able to transfer solutes. Nevertheless the CP seemingly attempts to maintain its 'epithelial soundness' when challenged to perform additional cleansing acts for the brain extracellular fluid (CSF).

                In healthly, young adults the CP epithelium sensitively acclimates to chemical and physical distortions in blood, CSF and parenchyma. Following cortical stabbing in rats, the CP upregulates TGFβ presumably to provide this CSF-borne growth factor for repairing the injury [38]. A similar phenomenon occurs with IGF-II [39], which is manufactured in the CNS mainly by CP. In diabetes there is enhanced expression of the NKCC1 cotransporter in CP for adjusting CSF dynamics and water distribution [40]. Such compensatory responses at the blood-CSF barrier in early adulthood raise the question about CP's ability in later life, when besieged by the deficits of aging and AD, to adequately respond by expressing certain 'homeostatic proteins'.

                Accordingly to assess pathophysiologic consequences of AD we investigated human CP's ability to upregulate certain functional proteins (as distinguished from structural ones) in advanced states of AD dementia. With advancing knowledge about intricate cell physiology (coordinated interactions among organelles, cytoplasm and membrane-bound proteins) it is relevant to evaluate components of cellular homeostasis. The term 'homeostatic proteins'refers to chaperones, receptors and transporters that stabilize the internal environment of the cell. CSF stability depends in large part upon CP epithelial homeostasis. Our group has analyzed several 'homeostatic proteins' involved in CP intracellular milieu stabilization:

                Heat shock proteins

                A wide spectrum of protection against neurodegeneration is provided by HSPs. The list of protective effects bestowed by HSP molecules is diverse and includes: accelerated degradation of misfolded proteins, maintenance of membrane lipid integrity, prevention of deleterious protein aggregation, and preclusion of damage to the translational apparatus [41, 42]. HSPs are also known as 'stress proteins' due to their role in shepherding adaptive responses to stressors such as ischemia, trauma, fever, dehydration, hydrocephalus and other brain disorders.

                To evaluate human CP expression, we selected HSPs overexpressed in AD brains: GRP94 and HSP90. In contrast to previously found upregulation in brain, there was downregulated GRP94 in lateral ventricle CP. In aged controls there was abundant staining in the epithelial cytoplasm and stroma (Fig. 2, top left). However in AD there was a striking decrease in immunostaining of GRP94 choroidal tissues (Fig. 2, top right). GRP94 is an atypical HSP in responding specifically to glucose deprivation rather than to generalized intracellular oxidative stress. In AD the opposite responses in GRP94 expression by CP vs. brain are interesting but not unexpected because secretory epithelium has biochemical characteristics fundamentally different from neurons. GRP94 chaperones protein folding, especially in endoplasmic reticulum [43]. Underexpressed GRP94 in CP of AD subjects may render the reticulum vulnerable to unfolded proteins.
                Figure 2

                Heat shock (stress) protein expression in human CP: Formalin-fixed, paraffin-embedded specimens (8–10 micrometers thick) were de-paraffinized and rehydrated. Sections were incubated overnight with antibodies against HSP90 (1/500; SPA830) and GRP94 (1/500;SPA850) and stained by the ABC technique (Vectastain Elite ABC peroxidase). Deposition of the brown chromogen (diaminobenzidine) reaction product was either substantially reduced by preabsorption blocking or virtually eliminated by omission of either primary or secondary antibodies. Slides were assessed blindly for staining intensity and distribution [37]. See text for description of localization and interpretation. For each HSP, images are representative of 10 AD specimens and 5 age-matched controls.

                In the case of HSP90, the reverse pattern of GRP94 was observed. There was faint staining of non-AD tissues (Fig. 2, bottom left) but strong expression in epithelial cytoplasm in AD CP (Fig. 2, bottom right). Multiple effects can be induced by a particular HSP. By complexing with several intracellular protein kinases, HSP90 could alter CSF secretion; and by inducing the heme-regulated e1F-2 alpha kinase, the overexpressed HSP90 may downregulate gene transcription [44]. Another possible effect of HSP90 is to beneficially accelerate clearance (reabsorption) of Aβ peptide by CP. Such facilitation occurs in the microglial handling of Aβ [45]. It would be worthwhile to pursue the role of CP HSPs in removing Aβ from CSF.

                FGF peptides and receptors

                The FGF superfamily of peptides and its multiple receptors in CP, ependyma, and brain, modulate many actions on neurons and non-neural cells [30]. FGF2, or basic FGF, is prototypic of the family. CP synthesizes and releases FGF2 into CSF. Choroidally-secreted FGF2 stimulates receptors (FGFr) nearby in the CP apical membrane [9] and at more distant sites in the brain parenchyma [46]. FGF/FGFr is apparently unique among growth factors in directly effecting balance in the brain fluids, including the formation of CSF. This is relevant to AD in which brain FGF is increased [47] and CSF turnover declines [1, 4, 6].

                FGF and FGFr are also fundamentally important in fostering neuron generation from stem cells in the subventricular zone (SVZ). This requires coordination between the CP-CSF and periventricular regions [46, 48]. Pharmacological manipulation of SVZ stem cells is potentially important at all stages of life. For pathological and therapeutic reasons, therefore, it is important to delineate FGFr expression patterns and their significance in i) ontogeny, ii) normal adult maintenance, and iii) neurodegeneration.

                i) Ontogeny

                Receptor plasticity in aging and AD is better seen in light of information on FGF/FGFr expression dynamics in early life. In the fetus the formation of CP, neuronal stem cells and brain is promoted by CP growth factor secretion and CSF distribution [46, 49]. Intense activity of FGF/FGFr figures prominently in CNS viability and expansion. Expression of FGFr-2 and -3 in murine CP is maintained prenatally, whereas FGFr-1 and -4 are present during the 2nd but not 3rd gestational week [49]. FGF peptides released from CP use autocrine and paracrine mechanisms to stimulate various forms of FGFr expressed by CP epithelium. Specific functions of the four different receptor isoforms need elucidation. Despite limited data for CP FGFr expression patterns in aging, the genetic regulation of FGFr during embryonic life [49] suggests the potential to pharmacologically enhance FGFr expression in AD. The goal in filling these knowledge gaps about FGFr is to attain more efficacious treatment of injuries to the brain interior.

                FGF2 derived from CP is also conveyed by CSF bulk flow to the fetal germinal matrix where it acts on stem cell FGFr to promote neuronal maturation [46]. By this endocrine-like mechanism, the CSF-mediated distribution of FGF2 and other peptides plays a prominent role in 'spawning' new neurons in the periventricular regions. Distorted CSF volume and flow in hydrocephalus interferes with the CSF provision of FGF2 to FGFr on stem cells in the SVZ [46]. Brain malformation ensues. Clearly the orderly function of the CP-CSF system, e.g., the programmed secretion and distribution of growth factors, is essential to normal CNS development.

                ii) Adult maintenance and response to stressors

                The FGF/FGFr system also has a key role in adult CNS fluid homeostasis. CP helps the brain adapt to alterations in blood composition and flow. In otherwise healthy young adults, the imposition of dehydration or sudden ischemia upon the CNS elicits striking adaptive changes in CP epithelium. To endure insults by chemical or physical stressors [29], it is critical that CP viability be maintained so that the brain can continue to benefit from 'homeostatic adjustments' in transport phenomena at the blood-CSF barrier [50]. Growth factors are an integral part of these adaptive responses to stress. Dehydration and ischemia are common to aging and AD. Elucidation of CP-CSF growth factor responses to these disorders in normal adults should enhance our perspective on homeostatic capabilities in AD.

                Dehydration seriously threatens CNS functions. Adjustments to dehydration in the healthy adult brain feature ion and water redistribution among fluid compartments. These compensatory responses to plasma hyperosmolality stabilize neuronal and interstitial volumes. Brain 'barriers' or transport interfaces are sites for the fluid homeostatic mechanisms. A working model for the restoration of fluid balance is offered: Dehydration or hyperosmolality upregulates the FGF2 and AVP peptides in CP [51, 52]. FGF2 released by CP binds in an autocrine manner to FGFr. Such FGFr stimulation likely promotes AVP release from CP epithelium [9]. The extruded AVP then binds V1 receptors in CP to regulate ion transport [53] and fluid production [10, 54]. FGF2 works in concert with AVP to control fluid movement across the blood-CSF barrier [51, 55]. Interestingly in AD there are upregulated receptors for FGF (Fig. 3) and AVP [56] in human CP, presumably in response to fluid imbalance. Cumulative evidence points to co-localized growth factors and neuropeptides jointly stabilizing brain fluids after perturbed osmolality and volume.
                Figure 3

                FGF receptor expression in human CP: Lateral ventricle plexuses obtained from pathologically-confirmed AD subjects were immersion-fixed in paraformaldehyde, cryoprotected and stored at -70°C. CP segments were free-floated for 72–96 hr in a 1/500 polyclonal antibody against the FGFr, which recognizes all FGF receptor subtypes. Specific staining was established by antibody omission/preabsorption [36]. ABC peroxidase/diaminobenzidine technique was used. Arrowhead points to small punctated dots of immunoreactivity. Localization of FGFr is described in text. Images are typical of those obtained from 8 controls and 8 AD specimens, respectively.

                Ischemia is another disorder with neuropathological consequences that are mitigated by growth factor upregulation or administration [57]. Bilateral carotid artery occlusion in young adult rats for 6–10 min wreaks damage to tissues surrounding the lateral ventricles [58, 59]. Hence severe transient forebrain ischemia (TFI) injures the lateral plexus as well as the hippocampus [60]. However peptides such as FGF2 and TGFβ defend the forebrain interior against ischemic and hypoxic insults [57, 58, 61]. Although TFI with hypotension (40 mmHg) destroys many choroidal epithelial cells [60], there is a role by growth factors to efficiently repair the breached blood-CSF barrier [60]. Restitution of the epithelial lining of the choroidal villi within several hours post-stroke [60] implies the importance of a functional CP for CNS viability. Upregulated secretion of FGF2, TGFβ [58] and other growth factors by CP [27] undoubtedly protects the blood-CSF barrier and periventricular brain against compromised blood flow. A time-course analysis of FGF2-FGFr expression in the aging vs. diseased CP will reveal how the blood-CSF interface responds to reduced blood flow in NPH and AD [62, 63].

                iii) Neurodegeneration

                FGF2 titers and FGFr receptor densities in degenerating CNS compartments provide insight on adaptive responses. FGF2 concentration is augmented in the AD brain [47]. Moreover with immunostaining and ELISA it was demonstrated that FGF2 levels in CP are sustained in AD [36]. It is thus probable that FGF2 and other factors secreted into CSF of aged adults are essential to forestalling harm to neurons in ischemia. A CSF feedback control system for the choroidal production of FGF2 has been suggested by FGFr identification in young adult rat CP [9]. An elevated level of FGF2 in AD brains [47] is interpreted as peptide sequestration from CSF [36], thereby lowering CSF concentration. Diminished CSF FGF2 could cause a compensatory increase in CP FGFr expression. Testing this postulate, we found enhanced staining for FGFr in AD CP epithelium (Fig. 3). This observation supports a role of the CP-CSF system in responding to increased demands by brain for FGF2. To build this model, information is needed for FGF2 and FGFr isoforms in various regions of the CNS and CSF at specific stages of dementia.

                FGF2 has an interesting relationship with amyloid. A worthwhile goal is to probe mechanisms of FGF2 interaction with amyloid in neuronal networks, extracellular matrix and CP-CSF. FGF2 co-localizes with several chemical forms of amyloid. Neuronal coexistence of FGF2 and amyloid precursor protein (APP) [64, 65] intimates a functional relationship between FGF2 and APP, perhaps in post-injury regeneration. FGF2 also minimizes metabolic injury caused by Aβ peptides. It was initially observed that FGF2 applied to cultured neurons reduced neurotoxicity of aggregated Aβ [66]. More recent findings confirm FGF2's benefit in abolishing neurotoxicity produced by Aβ1-43 [67] and attenuation of oxidative stress in hippocampal neurons induced by Aβ peptides [68]. In the extracellular matrix FGF2 competes with Aβ and APP for binding sites on heparan sulfate proteoglycans [69, 70]. This competitive binding by FGF2 may suppress interstitial amyloid plaque formation. Because the interstitium receives FGF2 from CSF, we predict that pharmacological boosting of CP secretion of FGF2 would relieve AD.

                FGF2-mediated protective regulation of CP transport phenomena potentially affects the course of neurodegeneration. Considerable evidence points to CP's ability to remove Aβ from CSF [7173]. This implicates reabsorptive transport at the blood-CSF barrier to reduce CSF Aβ burden in advanced AD. In clearing Aβ from the CNS, the CP epithelium is exposed to substantial amounts of Aβ with the potential to curtail energized ion transport and fluid formation. CP Na-K-ATPase, a key enzyme in CSF production [74], also enables the transport of organic compounds [13]. Significantly, FGF2 lessens the toxicity of Aβ on Na-K-ATPase activity and mitochondrial function in cultured hippocampal neurons [68]. Toxic Aβ loads on CP transporters might impair secretion. The resultant decrease in CSF volume transmission and turnover would further destabilize the CNS. However treatment of AD with FGF analogs and IGF-1 [75] holds promise for countering Aβ toxicity [68] by creating a better CSF 'metabolic environment' for CP and brain.

                Fluid-regulating proteins

                The diminished ability of CP to form fluid in advanced ageing and AD begs the question of how epithelial ion transport proteins are altered by distorted neurochemistry in senescence. In very old laboratory mammals the Na-K-ATPase activity of CP and the CSF generated by it are cut in half [26, 76]. Another ion-translocating protein coupled to CSF formation is the apical NaK2Cl cotransporter isoform1 (NKCC1). NKCC1 transports Na, K and Cl into and out of the choroidal epithelium [77], depending upon ion gradients and hormonal modulation. Versatile bidirectional transport via NKCC1 confers flexibility for regulating ion movements and concentrations in the CP-CSF. Fluid secretion at the blood-CSF interface is linked to ion fluxes mediated by the loop-diuretic sensitive NKCC1 [78, 79]. NKCC1 information is plentiful for laboratory animal CP-CSF [7884] but scarce for the human counterpart.

                The cation-Cl superfamily of cotransporters includes NKCC1 and consists of 7 isoforms that actively transport Na and/or K electroneutrally with Cl [85]. NKCC1 in CP has several functions, i.e., to regulate epithelial [Cl], stabilize CSF [K] and control fluid secretion [77]. The T4 antibody differentially stains the NKCC1 secretory isoform in the apical membrane but not the KCl isoform at the basolateral surface of CP. In brain fluid homeostasis the expression of NKCC1 in CP is likely sensitive to perturbations in CSF osmolality, choroidal epithelial cell volume/ ion concentrations, intracranial pressure and ventricular volume. To shed light on compensatory responses by the CP to disease, our group analyzed NKCC1 expression in congenital, high-pressure hydrocephalus; and in adult chronic, closer-to-normal pressure hydrocephalus in AD/NPH syndromes.

                The NKCC1 helps cells and organs adjust to disrupted fluid balance. One thus expects homeostatic upregulation of this CP cotransporter in AD with its altered CSF dynamics. For delineating NKCC1 expression we used the T4 antibody to immunostain CP at various stages of AD dementia. Robust staining of the lateral ventricle plexus (even at Braak stage V/VI) occurred in the apical membrane and cytoplasm (Fig. 4). In an earlier study of CP specimens from various mammalian species (unpublished data), we observed uniform and consistent staining of the apical membrane NKCC1. T4 staining of the cytoplasm was more variable. In the human CPs analyzed, however, there was consistent cytoplasmic staining in AD and age-matched controls (Fig. 4). This may represent cytoplasmic NKCC1 protein available for insertion into the apical membrane.
                Figure 4

                NaK2Cl cotransporter expression in human CP: Lateral ventricle plexuses were incubated with T4 (not thyroxine) antibody, which stains the secretory isoform 1 of the NaK2Cl (NKCC1) cotransporter protein. The T4 antibody (mouse monoclonal; 1:100) was from the University of Iowa Developmental Studies Hybridoma Bank (Iowa City, IA); the biotinylated secondary was a rat-absorbed horse antibody. Diaminobenzidine was used to develop the brown reaction product. Controls (negative staining results; not shown) involved omission of secondary and/or primary antibody. AD tissues were from patients at Braak stage V/VI (top right) and III/IV (bottom right). Images are representative of 6 CPs analyzed for AD (mean age of 76 yr) and 6 for age-matched controls (mean age of 76 yr). On average, the staining intensity of AD specimens was 50% greater than controls. The text describes staining localization. All photographs are at the same magnification.

                AD choroidal tissues had greater T4 staining than controls (Fig. 4). The apical NKCC1 (Fig. 5) is strategically positioned to sense physical changes in CSF resulting from AD deterioration. Changes in pressure [86] or volume represent potential stimuli for inducing NKCC1 in CP. Ventriculomegaly and transient elevations in ICP in AD and NPH may elicit a compensatory response in CP to downregulate CSF formation by promoting ion reabsorption via the NKCC1 (Fig. 5). This scheme fits the enhanced expression of NKCC1 in CP of HTx congenital hydrocephalus rats with ventriculomegaly [87]. ANP, AVP, angiotensin II, serotonin and catecholamines all reduce CSF formation rate [99]. Table 3 recapitulates the stimulating effect of these same agents on NKCC1 transport activity in various tissues [8894]. This prompts the hypothesis that CSF formation is decreased secondarily to enhanced reabsorptive uptake of Na, K and Cl by CP from CSF (Fig. 5). Information about protein levels and mRNA for NKCC1 should relate CP cotransporter expression with CSF dynamics, ICP and ventricular volume.
                Figure 5

                A working model for hydrocephalus-induced alterations in NKCC1 cotransporter expression in CP: Ion transport across basolateral and apical surfaces is driven by transmembrane ion gradients [74, 83]. Normally the net transport of Na, K, Cl, and HCO3 from choroid cell into CSF is integral to CSF production [5, 7]. However, we postulate that when CSF formation is inhibited by various neurohumoral agents there is stimulated (+) inward NaK2Cl flux from CSF into the cell; this would increase cytoplasmic Na and Cl concentration [77] thus creating a less favorable ion gradient for basolateral uptake of Na and Cl from plasma. Consequently, there is inhibited (-) basolateral ion uptake, and sequentially, reduced apical extrusion of Na into CSF [40]. Net effect = decreased CSF formation. Consistent with this idea are observations of enhanced expression of CP NKCCl in congenital hydrocephalus [87] and AD (Fig. 4), both of which are generally associated with lower rates of CSF formation. Agents in Table 3 (e.g., Ang II) simultaneously stimulate the inward and outward arms of NKCC1, but the former three times the latter, resulting in net inward flux of ions [discussed in ref. 93]. The model thus vectorially emphasizes the inward arm of the NKCC1 (large arrowheads) as the one primarily stimulated by agents that suppress CSF formation. We hypothesize that in hydrocephalus, with increased intracranial pressure and/or ventriculomegaly, there is an associated attenuation of fluid output by CP.

                Table 3

                Stimulation of NaK2Cl cotransport by hormones, neurotransmitters and peptides that inhibit choroid plexus-CSF formation

                Active agent



                Cotransport activity a


                Atrial natriuretic peptide



                http://static-content.springer.com/image/art%3A10.1186%2F1743-8454-1-3/MediaObjects/12987_2004_Article_3_IEq1_HTML.gif 82%


                Angiotensin II

                Aortic endothelium


                http://static-content.springer.com/image/art%3A10.1186%2F1743-8454-1-3/MediaObjects/12987_2004_Article_3_IEq1_HTML.gif 38%


                Arginine vasopressin

                Medullary TALb


                http://static-content.springer.com/image/art%3A10.1186%2F1743-8454-1-3/MediaObjects/12987_2004_Article_3_IEq1_HTML.gif 66%


                Serotonin agonistc


                Cell line

                http://static-content.springer.com/image/art%3A10.1186%2F1743-8454-1-3/MediaObjects/12987_2004_Article_3_IEq1_HTML.gif 49%


                Adrenergic agoniste

                Parotid gland epithelium


                http://static-content.springer.com/image/art%3A10.1186%2F1743-8454-1-3/MediaObjects/12987_2004_Article_3_IEq1_HTML.gif R5 stainingd


                Adrenergic agoniste

                Skeletal muscle (plantaris)


                http://static-content.springer.com/image/art%3A10.1186%2F1743-8454-1-3/MediaObjects/12987_2004_Article_3_IEq1_HTML.gif 1700%


                Basic fibroblast growth factor

                Aortic endothelium


                http://static-content.springer.com/image/art%3A10.1186%2F1743-8454-1-3/MediaObjects/12987_2004_Article_3_IEq1_HTML.gif 40%


                a Bumetanide-sensitive 86Rb uptake by cells

                b Thick ascending limb of kidney tubule

                c (-)-2,5-dimethoxy-4-bromoamphetamine

                d R5 antibody-detected phosphorylation of NKCC1 proportional to functional activity

                e Isoproterenol

                Other factors must be considered in interpreting the enhanced NKCC1 expression (Fig. 4). An alternative but not mutually exclusive explanation is that upregulated NKCC1 in AD helps to counter cell shrinkage [95] in CP (Table 2). Moreover, a rise in CSF [K] resulting from neuronal damage, would be buffered by the NKCC1 [77] and Na pump [96] in CP. Therefore it is possible that NKCC1 in CP is concurrently carrying out several physiologic responses to stresses imposed by aging and disease. The ventriculomegaly and reduced CSF formation rate observed in AD and NPH [4] are consistent with the upregulated NKCC1 in human CP. To corroborate the model, however, more data are needed for humans and animals to tightly link alterations in CP transport and fluid turnover with AD progression. Because HSP90 binds to NKCC1 and modulates its function [97], it is also of interest to explore how upregulated HSP90 in AD (Fig. 2) mechanistically relates to enhanced expression of NKCC1 (Fig. 4).

                The choroid plexus as a 'bioreactor' to brain diseases

                CP is highly equipped, homeostatically speaking, to help the brain adapt to the metabolic distortions of dementia. Injured neurons undergo compositional changes. These cellular perturbations are transmitted to the extracellular space and distort the interstitial fluid composition. Many catabolites in the interstitium eventually gain access to the ventricles where they contact the CPs. By accepting a host of CSF-borne molecules, for either transport or receptor stimulation, the CP mediates a wide scope of renal- and hepatic-like activities [13, 98]. This epithelial interface also integrates many neurohumoral activities of the endocrine and immune systems [98, 99]. Diseases afflicting the CNS generate injury metabolites and cytokines that are conveyed to the ependyma, pia-glia, arachnoid membrane and CP epithelium. These interfaces handle catabolites and peptide fragments [100] by reabsorbing them into the systemic circulation for clearance or by sequestering toxic substances in lysosomes for metabolic conversion. Harmful substances are thereby effectively removed from the brain-CSF system.

                Signaling molecules are also carried by CSF from diseased regions to the CP. There they bind to specific receptors in the apical membrane and consequently elicit a variety of bioreactive responses. Binding sites for a wide array of peptides, proteins and other organic substances abound in the mammalian CP [73]. Choroidal epithelial cells can thus be regarded as 'bioreactors' that respond to chemical changes in extracellular fluid. Their response includes the synthesis of peptides, growth factors and sundry molecules for homeostatically repairing injured neurons.

                Currently, little is known about the spectrum of responses by CP to the disrupted CNS homeostasis in AD. It would be informative to compare AD stages for expression abilities of CP vs. the ependyma and meninges. Differences as well as similarities are anticipated. The initial studies of gene expression in human CP reported herein reveal that in Braak stages V/VI there is still strong expression of HSP90 and NKCC1 (Figs. 2 &4). Therefore even though the CP in advanced AD shows extensive histopathology (Table 2) and has reduced enzymatic activities and fluid formation [4, 6, 26], it evidently retains the ability to react to biochemical perturbations by expressing housekeeping proteins. This stabilizing effect on the blood-CSF barrier epithelium enables regulatory phenomena that ultimately support AD-stressed neurons.

                Insight can be gained by investigating CSF neurochemical composition as a function of AD severity. Additionally it would be instructive to analyze how cultured CP epithelium reacts to 'pathological' CSF from patients at progressive Braak stages. The Z310 cultured cell line and primary cultures of CP are useful for such analyses [101, 102]. Given the significance of CP in facilitating repair of CNS structures, it should also be fruitful to analyze in vivo gene expressions that reflect pathophysiological interactions between CP-CSF and brain.

                How can CP and the regions it nourishes be protected from AD?

                Therapeutic strategies to halt CNS deterioration should include ways to defend the CP epithelium against the oxidative ravages of ageing and AD. Prolonging CP viability and work efficiency may be important in maintaining the well being of geriatric patients. Even without a cure for AD, if deleterious changes in the brain interstitium were minimized in the elderly by stabilizing the CP-CSF (as well as the BBB), then it might be feasible to prevent the early manifestations of AD (Braak stages I/II) from intensifying into the debilitating pathology of V/VI.

                One class of agents with considerable potential for AD therapeutics is the growth factor group. A useful paradigm for CSF growth factors and neuroprotection has evolved from experiments on transient forebrain ischemia in rats [59, 60]. The TFI experiments characterized the destructive effects of acute ischemia on the lateral ventricle CP and the nearby CA1 region of hippocampus [50]; and the time course of cell recovery (or death) in these adjacent regions protected (or not) by supplemental infusion of FGF2 via CSF prior to the ischemic insult [61]. Exogenous FGF2 administered before or after the induced ischemia lessened cell death in CA1, probably in part by stabilizing CP functions [28, 50, 61]. Moreover the CP substantially repaired its epithelial cell barrier by 24 hr post-TFI, even without supplemental FGF2 [60]. Collectively these findings manifest the impressive plasticity of CP to reconstitute itself after disruption; and reveal the potential therapeutic value of pharmacologically-administered growth factors to reduce harm to CP and hippocampus.

                Several other growth factors synthesized by CP and secreted into CSF should be explored in translational research dealing with interacting ischemia, hydrocephalus and AD [1, 4, 6, 28, 36, 50, 55, 103, 104]. Following TFI the CP upregulates TGFβ, another peptide that helps the CNS adjust to injury [58]. Consequently choroidally-manufactured growth factors in disease states can benefit the plexus locally (by autocrine and paracrine mechanisms) and the brain more globally (by endocrine-like bulk flow of CSF). Our ischemia findings for the CP-CSF-hippocampus compartments [27, 58, 60] relate to AD in that reduced blood flow to the ageing CNS exacerbates AD progression. Growth factor supplements (e.g., VEGF, NGF, IGF-II & HGF) could augment viability in AD-vulnerable regions by enhancing vascularization, preventing programmed cell death or promoting stem cell conversion in the subventricular zone (SVZ). Newly-formed neurons in the SVZ might then migrate to atrophic regions to replace destroyed cells. One pharmacologic approach to stall AD onset is to administer a combination of growth factors designed to increase neuroprotection while minimizing fibrosis [55]. We theorize that an optimal regimen of growth factors and neuropeptides would restore CP function or prevent further loss of homeostatic capabilities.

                A look towards pharmacologic manipulation of CP in AD dementia

                In searching for agents to modify CP epithelial protein expression, the route of delivery of the active drug is of primary importance. Unlike the brain with its impermeable microvessels, the CP readily takes up water-soluble drugs from the plasma due to the highly-permeable choroidal capillaries. Consequently water-soluble agents freely diffuse to receptors or binding sites at the basolateral surface of the epithelium. Access of blood-borne hydrophilic compounds to the CSF-side of CP however is problematic because the tight junctions and basolateral membrane impede diffusing molecules as small as mannitol [105]. Molecular sieving at the basolateral membrane restricts the permeation of hydrophilic molecules as small as urea (m.w. = 60) into the CP-CSF compartments [106].

                To circumvent the blood-CSF barrier, therapeutic agents are delivered into CSF by lateral ventricle catheters in experimental animals [55] or hydrocephalic patients. Gene therapy offers the additional challenge of finding a viral vector that selectively targets the CP epithelium for transduction [107]. Timely, innovative strategies are in order to find specific ways to target and improve CP function in neurodegenerative states.

                A compelling aspect of CSF translational research is to identify agents that effectively regulate fluid formation by CP. Whereas the difficulty in congenital hydrocephalus is to downregulate CSF formation, the challenge in AD is to enhance CSF turnover perhaps by accelerating fluid production as well as outflow. Augmented flow of CSF enhances 'sink action' [108, 109]. This would expedite clearance of toxic molecules like Aβ out of the brain interstitial fluid into the ventricles. New agents that stimulate CP to secrete CSF more rapidly should be tested in aged animals and those with AD-phenotypes. A consistent finding of decreased CNS burdens of Aβ in animals with increased CSF turnover could spur the development of drugs for brain 'cleansing' in AD.

                Another CP pathology meriting pharmacological attention is the massive fibrosis that progressively envelops the interstitium in old age. This interstitial fibrosis is even more extensive in AD [21]. Fibrosis undoubtedly impedes efficient movement of molecules between blood and CSF. It is pertinent to ascertain if therapeutic minimization of CP fibrosis in later life would permit a brisk turnover of CSF to be sustained. Attenuating the formation of Biondi bodies and other choroidal cellular inclusions (Table 2) would be a unique approach to prevent age- and disease-related curtailment of CSF production. Optimal vascular-interstitial-epithelial interactions in the CP are foundational for vigorous CSF dynamics. The longer the blood-CSF interface retains its epithelial secretory capabilities, the more successfully it can conduct homeostatic activities to ward off AD.

                Recapitulation and projections

                The CP has the main responsibility for CSF homeostasis. Therefore the functional status of the blood-CSF barrier is of great consequence to the CNS. Maintaining the CSF at a stable, specialized composition is of the utmost importance to neurons. CSF is prominent in regulating brain interstitial fluid with which it exchanges nutrients and waste products. Diseases markedly affect these molecular exchanges. Maintaining healthy bidirectional transport across the CP epithelium (CSF-blood) and ependyma (CSF-brain) is thus integral to a sound brain fluid environment.

                CSF macrocirculation through the ventriculo-subarachnoid system together with CSF microcirculation in the perivascular Virchow-Robin spaces [110, 111] perform distributive as well as collective functions. By gathering waste products, the CSF is a quasi-lymphatic system with critical functions in excreting harmful peptides and proteins. In early life the upregulated secretions of CP play a central role in brain ontogeny by furnishing growth factors to the germinal matrix. At the end of life with disease onset or aging consequences, the CP transporters are upregulated again to rescue failing neurons by providing neurotrophic materials to CSF. Equally important, peptides in excess such as amyloid beta (Aβ) fragments in AD must be eliminated from CNS by perivascular pathways [112]. To facilitate clearance of Aβ, the continual production of CSF by CP sustains 'sink action' on the brain interstitium [109].

                As the main generator of CSF, the CP has a pivotal role in helping the brain cope with the twin stressors of ageing and disease. More attention should be focused on the blood-CSF interface for pharmacologic opportunities to stave off CP dysfunction. Our findings on human CP expression of HSP90, FGFr and NKCC1 demonstrate that this epithelium in AD reacts to metabolic insults by upregulating certain proteins. This suggests that even diseased CP could respond to therapeutic agents, thus opening new vistas for treating CSF dysfunction in age-related dementias.


                Investigation of CP in AD is an area that is opening up. Translational research can now intensely focus on molecular factors that disable the CP to the point of reducing its ability to preserve brain integrity. Systematic CSF analyses using mass spectrometry and other cutting-edge biotechnology should generate neurochemical data specific for disease stages. New imaging approaches are essential to provide much needed functional data for CP, CSF and periventricular regions in AD patients. This should expedite the modeling of CP-CSF malfunctions and their resolution. Deeper insight into the pathophysiology of the blood-CSF transport interface will help to realize the development of novel therapeutic regimens for the AD family of diseases.

                Authors contributions

                CJ had the primary responsibility of organizing and writing the review, and had NIH support (NS 27601) to do the NaK2Cl cotransporter experiments. PM carried out the NKCC1 immunostaining runs with the T4 antibody and provided interpretation of the regional stainings. RT conducted the experimental analyses of the heat shock proteins and generated figures. AS did the image processing analyses of the cotransporter expression and assisted with the literature analysis. JD contributed ideas for the altered CP-CSF dynamics in hydrocephalus and ventriculomegaly. GS has developed the model that CP-CSF malfunction exacerbates AD progression, and helped to revise the manuscript. ES was responsible for the FGFr experiments and interpreted the human CP data. All authors read and approved the final manuscript.



                Alzheimer's disease


                amyloid precursor protein


                beta amyloid


                arginine vasopressin


                blood-brain barrier


                choroid plexus


                basic fibroblast growth factor 2


                receptor for fibroblast growth factor


                glucose regulatory protein 94


                heat shock protein 90


                nerve growth factor


                Na-K-2Cl cotransporter secretory isoform 1


                normal pressure hydrocephalus


                transforming growth factor beta


                subventricular zone


                transient forebrain ischemia


                vascular endothelial growth factor


                insulin-like growth factor II


                hepatocyte growth factor



                We thank H. Schipper and S. Anthony for valuable contributions to the stress protein investigation; V. Hovanesian for image processing; N. Johanson for editing; and V. Kuo-LeBlanc and C. Ayala for help with the immunohistochemistry. Gratitude for research support is expressed to: the Brown Neurosurgery Division, Lifespan/Rhode Island Hospital, and the NIH (grant NS RO1 27601).

                Authors’ Affiliations

                Department of Clinical Neurosciences, Brown Medical School
                Department of Pathology, Brown Medical School


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