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Structural and Quantitative Comparison of Cerebrospinal Fluid Glycoproteins in Alzheimer’s Disease Patients and Healthy Individuals

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Abstract

Glycoproteins in cerebrospinal fluid (CSF) are altered in Alzheimer’s Disease (AD) patients compared to control individuals. We have utilized albumin depletion prior to 2D gel electrophoresis to enhance glycoprotein concentration for image analysis as well as structural glycoprotein determination without glycan release using mass spectrometry (MS). The benefits of a direct glycoprotein analysis approach include minimal sample manipulation and retention of structural details. A quantitative comparison of gel-separated glycoprotein isoforms from twelve AD patients and twelve control subjects was performed with glycoprotein-specific and total protein stains. We have also compared glycoforms in pooled CSF obtained from AD patients and control subjects with mass spectrometry. One isoform of α1-antitrypsin showed decreased glycosylation in AD patients while another glycosylated isoform of an unassigned protein was up-regulated. Protein expression levels of α1-antitrypsin were decreased, while the protein levels of apolipoprotein E and clusterin were increased in AD. No specific glycoform could be specifically assigned to AD.

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References

  1. Nakagawa K, Kitazume S, Oka R et al (2006) Sialylation enhances the secretion of neurotoxic amyloid-beta peptides. J Neurochem 96:924–933

    Article  PubMed  CAS  Google Scholar 

  2. Liu F, Zaidi T, Iqbal K et al (2002) Role of glycosylation in hyperphosphorylation of tau in Alzheimer’s disease. FEBS Lett 512:101–106

    Article  PubMed  CAS  Google Scholar 

  3. Saez-Valero J, Fodero LR, Sjogren M et al (2003) Glycosylation of acetylcholinesterase and butyrylcholinesterase changes as a function of the duration of Alzheimer’s disease. J Neurosci Res 72:520–526

    Article  PubMed  CAS  Google Scholar 

  4. Robertson LA, Moya KL, Breen KC (2004) The potential role of tau protein O-glycosylation in Alzheimer’s disease. J Alzheimers Dis 6:489–495

    PubMed  CAS  Google Scholar 

  5. Botella-Lopez A, Burgaya F, Gavin R et al (2006) Reelin expression and glycosylation patterns are altered in Alzheimer’s disease. Proc Natl Acad Sci USA 103:5573–5578

    Article  PubMed  CAS  Google Scholar 

  6. Romeo MJ, Espina V, Lowenthal M et al (2005) CSF proteome: a protein repository for potential biomarker identification. Expert Rev Proteomics 2:57–70

    Article  PubMed  CAS  Google Scholar 

  7. Puchades M, Hansson SF, Nilsson CL et al (2003) Proteomic studies of potential cerebrospinal fluid protein markers for Alzheimer’s disease. Brain Res Mol Brain Res 118:140–146

    Article  PubMed  CAS  Google Scholar 

  8. Andreasen N, Minthon L, Davidsson P et al (2001) Evaluation of CSF-tau and CSF-Abeta42 as diagnostic markers for Alzheimer disease in clinical practice. Arch Neurol 58:373–379

    Article  PubMed  CAS  Google Scholar 

  9. Jobst KA, Barnetson LP, Shepstone BJ (1997) Accurate prediction of histologically confirmed Alzheimer’s disease and the differential diagnosis of dementia: the use of NINCDS-ADRDA and DSM-III-R criteria, SPECT, X-ray CT, and APO E4 medial temporal lobe dementias. The Oxford Project to Investigate Memory and Aging. Int Psychogeriatr 1(Suppl 9):191–222; discussion 247–252

    Article  Google Scholar 

  10. Itoh N, Arai H, Urakami K et al (2001) Large-scale, multicenter study of cerebrospinal fluid tau protein phosphorylated at serine 199 for the antemortem diagnosis of Alzheimer’s disease. Ann Neurol 50:150–156

    Article  PubMed  CAS  Google Scholar 

  11. Pan S, Wang Y, Quinn JF et al (2006) Identification of Glycoproteins in Human Cerebrospinal Fluid with a Complementary Proteomic Approach. J Proteome Res 5:2769–2779

    Article  PubMed  CAS  Google Scholar 

  12. Davidsson P, Paulson L, Hesse C et al (2001) Proteome studies of human cerebrospinal fluid and brain tissue using a preparative two-dimensional electrophoresis approach prior to mass spectrometry. Proteomics 1:444–452

    Article  PubMed  CAS  Google Scholar 

  13. Davidsson P, Westman-Brinkmalm A, Nilsson CL et al (2002) Proteome analysis of cerebrospinal fluid proteins in Alzheimer patients. Neuroreport 13:611–615

    Article  PubMed  CAS  Google Scholar 

  14. Hakansson K, Emmett MR, Marshall AG et al (2003) Structural analysis of 2D-gel-separated glycoproteins from human cerebrospinal fluid by tandem high-resolution mass spectrometry. J Proteome Res 2:581–588

    Article  PubMed  CAS  Google Scholar 

  15. Ogata Y, Charlesworth C, Muddiman D (2005) Evaluation of Protein Depletion Methods for the Analysis of Total-, Phospho- and Glycoproteins in Lumbar Cerebrospinal Fluid. J Proteome Res. Web Release Date:31–Mar-2005

  16. Finehout EJ, Franck Z, Lee KH (2004) Towards two-dimensional electrophoresis mapping of the cerebrospinal fluid proteome from a single individual. Electrophoresis 25:2564–2575

    Article  PubMed  CAS  Google Scholar 

  17. Finehout EJ, Franck Z, Lee KH (2005) Complement protein isoforms in CSF as possible biomarkers for neurodegenerative disease. Dis Markers 21:93–101

    PubMed  CAS  Google Scholar 

  18. Hu Y, Malone JP, Fagan AM et al (2005) Comparative proteomic analysis of intra- and interindividual variation in human cerebrospinal fluid. Mol Cell Proteomics 4:2000–2009

    Article  PubMed  CAS  Google Scholar 

  19. Castano EM, Roher AE, Esh CL et al (2006) Comparative proteomics of cerebrospinal fluid in neuropathologically-confirmed Alzheimer’s disease and non-demented elderly subjects. Neurol Res 28:155–163

    Article  PubMed  CAS  Google Scholar 

  20. Sihlbom C, Davidsson P, Emmett MR et al (2004) Glycoproteomics of cerebrospinal fluid in neurodegenerative disease. Inter J Mass Spectrom 234:145–152

    Article  CAS  Google Scholar 

  21. APA (1994) Diagnostical and statistical manual of mental disorders, 4th edn. American Phychiatric Association, Committee on Nomenclature and statistics, Washington, DC

    Google Scholar 

  22. WHO (1992) The ICD-10 classification of mental and behavioural disorders. WHO, Geneve

    Google Scholar 

  23. Sihlbom C, Davidsson P, Nilsson CL (2005) Prefractionation of cerebrospinal fluid to enhance glycoprotein concentration prior to structural determination with FT-ICR mass spectrometry. J Proteome Res 4:2294–2301

    Article  PubMed  CAS  Google Scholar 

  24. Shevchenko A, Wilm M, Mann M (1997) Peptide sequencing by mass spectrometry for homology searches and cloning of genes. J Protein Chem 16:481–490

    Article  PubMed  CAS  Google Scholar 

  25. Perkins DN, Pappin DJ, Creasy DM et al (1999) Probability-based protein identification by searching sequence databases using mass spectrometry data. Electrophoresis 20:3551–3567

    Article  PubMed  CAS  Google Scholar 

  26. Gollin PA, Kalaria RN, Eikelenboom P et al (1992) Alpha 1-antitrypsin and alpha 1-antichymotrypsin are in the lesions of Alzheimer’s disease. Neuroreport 3:201–203

    Article  PubMed  CAS  Google Scholar 

  27. Lomas DA, Stone SR, Llewellyn-Jones C et al (1995) The control of neutrophil chemotaxis by inhibitors of cathepsin G and chymotrypsin. J Biol Chem 270:23437–23443

    Article  PubMed  CAS  Google Scholar 

  28. Sun YX, Minthon L, Wallmark A et al (2003) Inflammatory markers in matched plasma and cerebrospinal fluid from patients with Alzheimer’s disease. Dement Geriatr Cogn Disord 16:136–144

    Article  PubMed  CAS  Google Scholar 

  29. Teunissen CE, de Vente J, Steinbusch HW et al (2002) Biochemical markers related to Alzheimer’s dementia in serum and cerebrospinal fluid. Neurobiol Aging 23:485–508

    Article  PubMed  CAS  Google Scholar 

  30. Johnson G, Brane D, Block W et al (1992) Cerebrospinal fluid protein variations in common to Alzheimer’s disease and schizophrenia. Appl Theor Electrophor 3:47–53

    PubMed  CAS  Google Scholar 

  31. Lidstrom AM, Hesse C, Rosengren L et al (2001) Normal levels of clusterin in cerebrospinal fluid in Alzheimer’s disease, and no change after acute ischemic stroke. J Alzheimers Dis 3:435–442

    PubMed  CAS  Google Scholar 

  32. Strittmatter WJ, Saunders AM, Schmechel D et al (1993) Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease. Proc Natl Acad Sci USA 90:1977–1981

    Article  PubMed  CAS  Google Scholar 

  33. Hesse C, Larsson H, Fredman P et al (2000) Measurement of apolipoprotein E (apoE) in cerebrospinal fluid. Neurochem Res 25:511–517

    Article  PubMed  CAS  Google Scholar 

  34. Nilsson CL (2005) High-resolution mass spectrometric approaches to glycoprotein characterization. In: Marko-Varga G (ed) Proteomics and peptidomics-technology developments driving biology. Elsevier, Amsterdam, pp 411–428

    Google Scholar 

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Acknowledgments

The authors thank Dr. Hasse Karlsson, Inst Biomedicine, Goteborg University, for the nano-LC setup and good advice on mass spectrometry and data assignment. This work was supported by DMR 0084173, Swedish Research Council and Wilhelm och Martina Lundgrens stiftelse. The purchase of the LTQ-FT-ICR mass spectrometer was made possible through a grant from Knut and Alice Wallenberg Foundation (C. L. Nilsson and R. A. Zubarev).

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Correspondence to Carina Sihlbom.

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Sihlbom, C., Davidsson, P., Sjögren, M. et al. Structural and Quantitative Comparison of Cerebrospinal Fluid Glycoproteins in Alzheimer’s Disease Patients and Healthy Individuals. Neurochem Res 33, 1332–1340 (2008). https://doi.org/10.1007/s11064-008-9588-x

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  • DOI: https://doi.org/10.1007/s11064-008-9588-x

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