- Open Access
Protein profiling reveals inter-individual protein homogeneity of arachnoid cyst fluid and high qualitative similarity to cerebrospinal fluid
Fluids and Barriers of the CNSvolume 8, Article number: 19 (2011)
The mechanisms behind formation and filling of intracranial arachnoid cysts (AC) are poorly understood. The aim of this study was to evaluate AC fluid by proteomics to gain further knowledge about ACs. Two goals were set: 1) Comparison of AC fluid from individual patients to determine whether or not temporal AC is a homogenous condition; and 2) Evaluate the protein content of a pool of AC fluid from several patients and qualitatively compare this with published protein lists of cerebrospinal fluid (CSF) and plasma.
AC fluid from 15 patients with temporal AC was included in this study. In the AC protein comparison experiment, AC fluid from 14 patients was digested, analyzed by LC-MS/MS using a semi-quantitative label-free approach and the data were compared by principal component analysis (PCA) to gain knowledge of protein homogeneity of AC. In the AC proteome evaluation experiment, AC fluid from 11 patients was pooled, digested, and fractionated by SCX chromatography prior to analysis by LC-MS/MS. Proteins identified were compared to published databases of proteins identified from CSF and plasma. AC fluid proteins not found in these two databases were experimentally searched for in lumbar CSF taken from neurologically-normal patients, by a targeted protein identification approach called MIDAS (Multiple Reaction Monitoring (MRM) initiated detection and sequence analysis).
We did not identify systematic trends or grouping of data in the AC protein comparison experiment, implying low variability between individual proteomic profiles of AC.
In the AC proteome evaluation experiment, we identified 199 proteins. When compared to previously published lists of proteins identified from CSF and plasma, 15 of the AC proteins had not been reported in either of these datasets. By a targeted protein identification approach, we identified 11 of these 15 proteins in pooled CSF from neurologically-normal patients, demonstrating that the majority of abundant proteins in AC fluid also can be found in CSF. Compared to plasma, as many as 104 proteins in AC were not found in the list of 3017 plasma proteins.
Based on the protein content of AC fluid, our data indicate that temporal AC is a homogenous condition, pointing towards a similar AC filling mechanism for the 14 patients examined. Most of the proteins identified in AC fluid have been identified in CSF, indicating high similarity in the qualitative protein content of AC to CSF, whereas this was not the case between AC and plasma. This indicates that AC is filled with a liquid similar to CSF. As far as we know, this is the first proteomics study that explores the AC fluid proteome.
Arachnoid cysts (AC) are benign intracranial lesions with a reported prevalence in the adult population of up to 1% [1, 2]. AC can be found all along the cranio-spinal axis, but have a marked predilection for the temporal fossa . Anatomically, ACs are formed by a splitting of the arachnoid mater (AM) creating a potential space that when filled with fluid appears as a cyst [4, 5]. Temporal ACs are classified according to Galassi et al. . Briefly, a type I cyst is small, biconvex, and located at the anterior temporal pole. A type II cyst involves the proximal and intermediate segments of the Sylvian fissure, and a type III cyst involves the entire Sylvian fissure and has often a marked radiological mass effect. The cyst wall is composed of non-neoplastic arachnoid cells with a capacity to secrete fluid [7, 8] that slightly differs in chemical composition from that of cerebrospinal fluid (CSF) . The genetic profile of temporal AC membranes  indicates that these cysts represent a homogenous condition, but the underlying cause of AC formation is unknown. Further analyses of the cyst fluid with proteomics, the large-scale studies of proteins, might give indications of the aetiology of AC and thus shed further light on the mechanisms underlying fluid secretion and transport.
One aim of this study was to compare the protein content of cyst fluid from temporal AC of different individuals using proteomics (AC protein comparison experiment). Our hypothesis was that AC is a homogenous condition, and that we could identify a similar protein profile from AC from different patients. Homogenous protein content between AC fluid from different patients would point towards similar filling mechanisms for the examined patients. Large differences in some patients would indicate different filling mechanisms in these patients. Such a difference, if present, would be revealed by a label-free proteomics comparison approach. Mass spectrometry-based label-free approaches are commonly used for semi-quantitative comparison of complex protein samples .
Another aim of the study was to identify the major proteins present in AC fluid and examine if these proteins also appeared in CSF and plasma (AC proteome evaluation experiment). For the proteins that did not appear in the CSF and plasma protein databases, we used a targeted mass spectrometry protein identification approach referred to as MIDAS in an attempt to identify these AC fluid proteins in CSF. The protein content of AC fluid is largely unknown, but it has been shown to have reduced protein content relative to that of CSF from the same patient, as evaluated by clinical chemistry . In a similar study, Sandberg et al. studied the clinical chemistry of AC fluid in pediatric patients. We did not have specific hypotheses on the degree of similarity of AC fluid to CSF or plasma, as this has not been thoroughly demonstrated in literature. This AC fluid protein identification part of our study and comparison with CSF and plasma might give information about the origin of the AC fluid and the mechanisms of filling and sustaining of AC.
Participants and collection of AC fluid and CSF
15 patients (six male, nine female, age 22-77 y) with unilateral, temporal AC were included in the study. AC fluid was collected during surgery for AC at Haukeland University Hospital (Bergen, Norway). The patients' characteristics are summarized in Table 1. One patient (No. 3) had previously been operated for a chronic subdural hematoma, most probably caused by the cyst , and another patient (No. 4) had undergone previous surgery for the AC. The other patients had no previous history of intracranial hematomas or surgery. The sample collection and handling protocol used in this study have been described in detail elsewhere [9, 14]. Briefly, AC fluid was collected during elective surgery for AC (craniotomy with fenestration and extirpation of the cyst) by puncturing the dura with a 23G, 25 mm long syringe needle using an Optidynamic® spinal fluid manometer (Mediplast AB, Malmo, Sweden) by siphoning through a burr hole before the craniotomy/opening of the dura. This procedure ensures that CSF does not contaminate the collected AC fluid: The remaining fluid in the cyst was removed by suction during opening of the cyst wall. The collected AC fluid was centrifuged at 450 × g for 5 min to remove cells and cell debris, and the supernatant was aliquoted and frozen at -80°C. Deviations and observations on individual sample material were noted on sampling. During this sampling, slight hemolysis was observed in one patient sample (No 12). The CSF used for the targeted AC protein identification experiment was collected under informed consent as lumbar CSF before spinal anaesthesia in patients undergoing lower extremity orthopedic surgery from neurologically healthy individuals. The CSF was handled by the same protocol as for the AC fluid, and the CSF used in this experiment was pooled from 11 individuals.
Patients were recruited by the responsible surgeon and signed a written informed consent. This project was approved by the Regional Committee for Medical and Health Research Ethics (REK) of Western Norway (approvals REK 70.03, NSD 9634, REK 151.06 and REK 2009/1885).
Trypsin was purchased from Promega (Fitchburg WI, USA). Urea, acetonitrile (ACN), formic acid (FA), calcium chloride (CaCl2), iodoacetamide (IAA) and dithiothreitol (DTT), potassium phosphate monobasic (KH2PO4), potassium chloride (KCl), water and trifluoroacetic acid (TFA) were purchased from Sigma-Aldrich (St. Louis MO, USA). Water and ACN were of HPLC quality.
Sample preparation and protein digestion
The protein concentration in AC fluid was measured using a Qubit™ fluorometer (Life Technologies, Carlsbad CA, USA). AC fluid was concentrated and desalted using Amicon 3 kDa molecular weight cut-off filters (Millipore, Billerica, MA, USA) and dried in a vacuum concentrator (Eppendorf, Hamburg, Germany). The proteins were digested into peptides using in-solution digestion, as follows: The dried protein pellet was dissolved in 6 M Urea and 100 mM DTT and incubated for 1 h at 37°C. Cysteins were alkylated using 200 mM iodoacetamide and the samples were incubated for 1 h at 37°C. Chymotrypsin activity was inhibited by adding 2 mM CaCl2 the proteins were digested to peptides over night using a protein:trypsin ratio of 1:50. Each sample was acidified using 5% TFA to quench the digestion activity, followed by drying the sample completely in a vacuum concentrator.
Strong cation exchange (SCX) chromatography
The samples were dissolved in 120 μL of SCX loading buffer (5 mM KH2PO4, 25% ACN, 0.05% FA, pH = 3) and fractionated by SCX chromatography using an Ultimate 3000 LC system (Dionex, Ultimate, Sunnyvale, CA, USA) equipped with a BioBasic SCX column (150 mm × 2.1 mm, 5 μm, Thermo Scientific, Ontario, Canada). The peptides were eluted in SCX elution buffer (500 mM KCl, 5 mM KH2PO4, 25% ACN, 0.05% FA, pH 3.0) over 55 min with a flow rate of 0.2 mL/min. A total of 28 SCX fractions were collected. The first two fractions (SCX fraction 1 and 2) were collected with 5.5 min intervals (first 11 min) and the last fraction (fraction number 28) was collected over the last 5 min. Fractions number 3-27 was collected with 1.5 min intervals. After collection, each SCX fraction was vacuum concentrated to dryness.
The samples were desalted using a 96 well reverse phase Oasis® HLB μElution Plate 30 μm (Waters, Wilford, MA, USA). The wells in the μElution plate were conditioned with solvent B (80% ACN, 0.1% FA) and thereafter washed twice with solvent A (0.1% FA). The peptides were re-suspended in solvent A, added to the μElution plate, and washed thrice with solvent A before the peptides were eluted twice using solvent B. One-minute centrifugation at 200 × g was used for all centrifugation steps except for addition of sample where 3 min at 150 × g was used. The samples were concentrated to dryness under vacuum and frozen at -80°C prior to mass spectrometry (MS) analysis.
In the AC protein comparison experiment, the peptides were dissolved in 0.1% FA, and 4 μL (1.6 μg) of the sample was injected onto a 40nL enrichment column (Zorbax 300SB C18 5 μm, Agilent Technologies, Santa Clara, CA, USA) at a flow rate of 3 μL/min using 3% ACN, 0.1% TFA. The separation column (0.0075 × 43 mm Zorbax 300SB C18 5 μm, Agilent Technologies) was used with the following gradient and a flow rate of 300 nL/min using solvent A (0.1% FA) and solvent B (90% ACN, 0.1% FA): 3-15% solvent B for 3 min, 15-45% solvent B for 42 min, 45-90% solvent B for 5 min and back to 3% solvent B after 5 min. Both columns were integrated in a CHIP (Agilent Technologies, Santa Clara, CA, USA), and an 1100 cap/nano HPLC coupled to a chip-cube-LC/MSD XCT Plus ion trap mass spectrometer (Agilent Technologies, Santa Clara, CA, USA) was used for separation and analysis, respectively. MS data was acquired using the AutoMS2 mode of the three precursors with highest intensity active exclusion for 1 min.
For the AC proteome evaluation experiment, the peptides were dissolved in 0.1% FA and 5 μL of the sample was injected to the analytical fused-silica capillary column (15 cm long, 75 μm i.d.) packed with Reprosil-Pur 3 μm C18 resin (Dr. Maisch, Ammerbuch-Entringen, Germany). The settings for LC were: Trap column: 2% ACN, 0.1% FA with a flow rate of 25 μL/min. Analytical column: solvent A was 0.1% FA and solvent B was 90% ACN, 0.1% FA. The flow rate was 0.288 μL/min with the following gradient: 5-12% solvent B for 2 min, 12-30% solvent B for 48 min, 30-50% solvent B for 20 min, 50-95% solvent B for 1 min and 95% solvent B was kept constant for 5 min before regeneration of the column for 24 min. The nano-HPLC system (Dionex, Ultimate, Sunnyvale, CA, USA) was coupled to an Ultima Global ESI-Q-TOF mass spectrometer (Waters, Wilford, MA, USA). The scan area for the MS survey scan was m/z 300-1500 with automatic fragmentation of the three ions with highest intensity. All the data was acquired in data dependent mode.
For the targeted AC protein identification experiment, the tryptic peptides of CSF from neurologically normal patients were dissolved in 0.1% FA and 1 μL was injected into the Q-TRAP 5500 (AB Sciex, Foster City, CA, USA) coupled to a nano-HPLC system (Dionex, Ultimate, Sunnyvale, CA, USA). The targeted mass spectrometry analysis was done using the MIDAS (Multiple Reaction Monitoring (MRM) initiated detection and sequence analysis) workflow  selecting a minimum of 3 peptides per protein, and three transitions per peptide based on information from in silico digestion. The instrument settings were 15 ms dwell time with approximately 3.5 s cycle time for 100 transitions per method in four analyses. MRM was then used as a survey scan in information dependent acquisition (IDA) to detect specific peptide peaks, and each resulting MRM peak was examined by two full MS/MS-scans to obtain sequence verification of the hypothesized peptide.
Mass spectrometry data analysis
For the AC protein comparison experiment, the raw data was processed with the Spectrum Mill search engine (Rev A.03.03.084) (Agilent Technologies, Santa Clara, CA, USA) using Carbamidomethylation (C) as fixed modification. The precursor mass tolerance was set to 2.5 Da with a product mass tolerance of 0.7 Da, and two trypsin miss-cleavages were allowed. The default autovalidation settings were applied for both protein and peptide level validation. Briefly, peptides were accepted at charge +2 if score >11 and%SPI >60 and at charge +3 if score >13 and%SPI >70. Proteins with a score >20 were accepted. A threshold of 2 was set both for peptides and proteins for the forward-reverse score and the rank 1-2 score, except for charge +2 with score >6 and%SPI > 90 where the threshold was 1.
For the AC proteome evaluation experiment, the mass list was extracted into PKL files with Masslynx (Waters, Wilford, MA, USA) and the PKL files were merged into a single MGF file using PklFileMerger . All MS/MS data were searched using the MASCOT (version 2.2.2) software platform (Matrix Science, London, UK) against the IPI-human database (v3.69, 174784 entries). Missed cleavages were set to one using trypsin as the enzyme. Carbamidomethyl (C) was set as fixed modification whereas Oxidation (M) was set as variable modifications. The peptide tolerance was set to 40 ppm and the MS/MS tolerance was set to 0.6 Da. Protein organization and redundancy reduction was done using the Scaffold software (v3.00.02 ). Peptide and protein identifications were accepted when the probability of correct identification was greater than 95%, with a minimum of two identified peptides per protein.
To verify peptide specificity in designated protein targets in the targeted AC protein identification experiment, MS/MS spectra were extracted using Analyst software (version 1.5) (Life Technologies, Carlsbad CA, USA). The selected spectra were searched using the MASCOT (version 2.3.0) software platform (Matrix Science) against the IPI-human database (version 3.78, 302626 entries) using precursor mass and MS/MS tolerance at 0.2 Da. Carbamidomethyl (C) was set as fixed modification and 0 miss cleavages were chosen.
The protein list from the AC fluid pool created in the AC proteome evaluation experiment was compared to published proteome libraries of CSF  and plasma . Database comparison was performed using ProteinCenter, v220.127.116.11 (Proxeon, Odense, Denmark). The grouping of proteins and analysis of molecular function and biological processes was performed in ProteinCenter, where gene ontology terms linked to specific proteins are obtained using mappings from the Gene Ontology Consortium website .
Principal component analysis (PCA) is a mathematical method that transforms a number of possibly correlated variables into a smaller number of uncorrelated variables called principal components, with the objective of improved understanding of the data . The algorithm of PCA gives the weight of each principal component, meaning the percentage of variation in the dataset explained. In the AC protein comparison experiment, the protein content between individual samples was compared based on spectral intensities. The spectral intensities in each sample were normalized based on the total sum of all intensities in that sample relative to a chosen reference samples. The protein hits from the AC protein comparison experiment were sorted according to protein score. To check for possible outliers, we first did a PCA including all identified proteins in the analysis, and plotted the patients according to the two first principal components. Next, we compared the samples based on the 50 proteins with highest protein score to avoid large influence from proteins identified in a low number of samples. Finally, we used a sub-sampling scheme [22, 23] consisting of two steps:
1- select 50 proteins at random and measure the distance normalized to standard deviation from the origin of each patient and 2 - repeat the first step 1000 times, and calculate the average distance from the origin over the 1000 replications.
This analysis was designed to reveal the degree to which any particular sample is divergent from the rest. Statistics was performed in the statistical software package R, version 2.11.1. (The R Foundation for Statistical Computing, Vienna, Austria).
A flow chart of the two main experiments conducted in this study, the AC protein comparison experiment and the AC proteome evaluation experiment is given in Figure 1.
The AC protein comparison experiment
In the AC protein comparison experiment the protein contents of AC fluid from 14 patients (patients 1-14) were semi-quantitatively compared using a label-free proteomics approach to determine the protein homogeneity across the different patients. The peptides from each of the 14 patients were analyzed on an ion-trap mass spectrometer, and the protein extracted ion chromatographic (XIC) intensity values, extracted from the Spectrum Mill searched data, were compared between the different patients using PCA. In total, 139 proteins were identified from the 14 different patients. When all 139 proteins were compared using PCA, the two first principal components (PC) explained 33% of the total variation in the dataset (Figure 2). As low scoring proteins with few associated spectra can lead to more inaccurate semi-quantitative measurements, we also compared the 50 proteins with highest protein scores. For this dataset, the two first PCs explained 48% of the total variation in the dataset (Figure 3). This was a larger degree of explained variation than the model based on all 139 proteins. A comparison based on the 50 highest scoring proteins gave a clearer separation in absolute distance from the origin for samples from patients 3 (old hematoma), 4 (previous operation) and 12 (slight observed hemolysis), as well as possibly patient 9, than for the other patients. To check whether or not this separation was due to a single or a few proteins, we performed a sub-sampling scheme. Selecting 50 of the 139 proteins at random for 1000 iterations and evaluating absolute distance in standard deviations from the origin showed that patients 3, 4 and 12, the samples presumed to be different, are consistently further away from the sample mean than the rest of the patients (Table 2), while this was not the case for patient 9. Disregarding patients 3, 4 and 12, the dataset of individual patient's AC fluid samples presents little systematic variation. We did not find that a few specific proteins create the separation of patients 3, 4 and 12 from the others. There was no apparent sub-grouping or trends in the data. The lack of systematic trends is an indication of homogenous sample material, thus suggesting that AC is a homogenous condition as evaluated by proteomics.
The AC proteome evaluation experiment
In the AC proteome evaluation experiment, the aim was to identify the major protein components of AC fluid, and to qualitatively compare these proteins to the proteins previously identified in CSF and plasma and thereby learn more about the composition and origin of AC fluid. Based on the results in the AC protein comparison experiment, AC fluid from patients with identified blood protein haemoglobin in the cyst fluid was excluded from this analysis (patients 7, 12, 13 and 14). In this experiment, 10 μg AC fluid from the remaining 11 patients was pooled, digested, fractionated using SCX chromatography, purified and analyzed on a Q-ToF mass spectrometer. From these analyses, 199 proteins were identified in the AC fluid (Additional File 1: List of 199 proteins detected in a pool of AC fluid from 11 patients, with number of peptides and sequence coverage). The identified proteins spanned a large range of MWs, with apolipoprotein C-I being the smallest with a MW of 9.3 kDa, and protocadherin fat 2 being the largest with a molecular weight of 479.3 kDa. The isoelectric point of the proteins ranged from 4.35 to 9.96, represented by cell growth regulator with EF hand domain protein 1 and NANUC-1 heavy chain protein, respectively. The MW and pI calculations were performed using the Compute pI/Mw tool . The 199 identified proteins were compared based on IPI accession numbers to published libraries of CSF  and plasma  (Figure 4). The database comparison identified 15 proteins that were not reported in CSF or plasma and we identified 11 of these by targeted protein identification in lumbar CSF samples using the MIDAS workflow on a Q-TRAP 5500 mass spectrometer (Table 3). Hence, most proteins identified in AC fluid (195 out of 199) were proven to also be present in CSF or plasma. The four proteins that were not found in the databases were; Isoform 3 of seizure 6-like protein 2, full-length cDNA clone CS0DD006YL02 of neuroblastoma of Homo sapiens, isoform 2 of neuroendocrine protein 7B2, and cell adhesion molecule 1 (Table 3). The overlap between AC fluid and plasma only contained 3 supplementary proteins not identified in CSF, whereas CSF and AC fluid had 89 proteins in common but not found in plasma (Figure 4). The 199 identified proteins identified in AC fluid were annotated to a diverse range of biological processes, molecular functions, and sub cellular compartments using the ProteinCenter, v18.104.22.168 software (Proxeon, Odense, Denmark) (Figures 5 and 6 and 7). Of the 199 proteins we identified, 39.6% are involved in transport as a cellular activity (Figure 5), 20.6% are involved in transport activity on molecular function (Figure 6), 81.9% are annotated as extracellular proteins, while 66.8% are membranous proteins (Figure 7). A comparison of molecular functions of the proteins identified in AC and CSF demonstrated a similar distribution (Figure 8). Ten genes have previously been found to be differentially expressed in AC membranes compared to normal arachnoid; NKCC1  and ASGR1, DPEP2, SOX9, SHROOM3, A2BP1, ATP10D, TRIML1, BEND5 and NMU . We did not find the corresponding protein products among the 199 identified proteins in our study.
As far as we know, this is the first study of proteomic evaluation of AC fluid. In the AC protein comparison experiment we looked for systematic differences or distributions between AC from different patients. The hypothesis underlying this experiment was that the protein profile in AC fluid would be similar between the examined patients, and this was supported by our data. This indicates a common filling mechanism and source for AC fluid in these patients. Previous observations of left side domination in males as well as a predilection for the middle cranial fossa do imply a common origin of AC fluid between patients. One possible method of formation is a defect during the embryological development of the Sylvian fissure . AC could potentially be two or more conditions or subgroups with different filling mechanisms but our proteomics data from the different samples of AC fluid did not support this hypothesis, as no systematic variation in PCA-plots was observed (Figures 2, 3). This finding supports previous experiments performed by clinical chemistry  and mRNA . We observed some variation for patients 3, 4 and 12, which can be explained by patient 3 having an old hematoma in close proximity and patient 4 previously operated for the same condition. Patient 12 had a slight observed haemolysis of the AC fluid. We had anticipated a change in the proteome as a consequence of a local trauma and consecutive repair mechanisms.
There was an increase in the percentage variation explained by the first two PCA components when looking at only the 50 highest scoring proteins compared to all 139 proteins. This can be explained by the fact that low scoring proteins often are represented by few peptide observations, which will lead to few values for semi-quantitative measurements, and the uncertainty in the measurements is increased. Hence, focusing only on the proteins with the highest protein scores will give a more accurate picture of the comparison. The method of sub-sampling was useful for evaluation of the stability of a result, such as for the evaluation on whether patient 9 was an actual outlier relative to the remaining patient samples.
The AC proteome evaluation experiment resulted in the identification of 199 proteins from pooled AC fluid from 11 patients. In order to identify more AC proteins than the 199 we found in our study, more extensive fractionation of the sample material could have been done, although this is limited by amount of sample material, as well as use of mass spectrometers with higher sequencing capacity and sensitivity. Using lumbar CSF as the basis for comparison with AC fluid is possible when doing a qualitative protein comparison, as proteins are not expected to disappear during migration towards the lumbar area. In a quantitative study between AC fluid and CSF on the other hand, it would be important to use CSF collected in the temporal fossa to avoid effects of the rostro-caudal protein gradients. Of the 199 proteins we identified 15 were not found among the reported 2627 proteins in the CSF database  or the 3017 in the plasma database . This does, however, not imply that these proteins are not present in CSF or plasma, as they may not have been previously identified and therefore not added to the database or they could be in the database but under a different accession number, leading to a mismatching. This may explain why we identified 11 of the 15 AC fluid proteins not found in the CSF or plasma databases, in the collected CSF samples, using targeted identification with the MIDAS workflow. Hence the number of proteins that potentially are unique to AC fluid was further decreased to four proteins after this experiment.
The large overlap between AC fluid proteins and CSF (192 of 199 proteins in common) indicates that CSF is important in the filling of the AC. There was much less overlap between identified plasma proteins and AC fluid proteins, with 104 proteins only identified in AC fluid. As the identified protein content of AC almost completely overlapped with the proteins previously identified in CSF, it was not surprising that the biological function annotation of the identified AC fluid also corresponded well with the annotations of the CSF proteins (Figure 8). We did not observe that any particular protein group was not present in AC fluid compared to CSF. In addition small (9.3 kDa), large (479.3 kDa), basic (pI 9.96), and acidic (pI 4.35) proteins were observed in AC fluid, indicating that there were no absolute exclusion of proteins with these different characteristics even though the most extreme basic and acidic proteins were not observed. Certain protein groups could be expected to not be present in AC if there was a selective transport mechanism of fluid across the AC membrane. There could, however still be quantitative differences between certain protein groups in CSF and AC fluid, which would then point towards properties in the filling mechanism. Given the high qualitative similarity we found between AC fluid proteins and CSF proteins, a relevant future study would be to do a quantitative protein comparison of the temporal fossa CSF and AC fluid from the same patient collected at the same time. This would give information about which proteins or protein classes that are differentially expressed between AC fluid and CSF in proximity to the AC, possibly giving further indications of the filling mechanism of AC fluid and the origin of the AC fluid.
The results of this study indicate that AC fluid is homogenous between patients when evaluated by protein content using a label-free semi-quantitative proteomics approach, a finding supporting results from previous experiments regarding clinical chemistry and mRNA. This points towards a similar filling mechanism of the AC for the examined patients. We found that most proteins identified in AC fluid also could be identified in CSF, while plasma had fewer proteins in common with AC fluid. This indicates that CSF has similar properties to AC fluid. We did not find specific groups of proteins with given properties absent from AC fluid, but there could still be different quantitative trends between CSF and AC fluid. A future quantitative proteomics comparison between CSF and AC collected from the same patients at the same time would reveal this information.
high pressure liquid chromatography
information dependent acquisition
multiple reaction monitoring initiated detection and sequence analysis
multiple reaction monitoring
principal component analysis
parts per million
strong cation exchange
trichloro formic acid
extracted ion chromatographic intensity value.
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The study was funded by the Western Norway Regional Health Authority (Helse Vest RHF) and by research allocations from The Meltzer foundation. The study was also supported in part by the National Program for Research in Functional Genomics (FUGE) funded by the Norwegian Research Council. MB thanks the operation theatre staff (SOP) at Haukeland University Hospital for a positive and helpful attitude towards the project.
The authors declare that they have no competing interests.
MB, ACK, KW, RJU, CAH, FSB conceived and designed the experiments. ACK, TTA, JAO, EO performed the experiments. MB, ACK, ØAH, TTA analyzed the data. KW, CAH operated on the patients. MB performed sample collection and handling. MB, ACK, ØAH, TTA, JAO, EO, KW, RJU, CAH, FSB wrote the paper. All authors read and approved the final manuscript.
Authors’ original submitted files for images
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