Insights into the human brain proteome: Disclosing the biological meaning of protein networks in cerebrospinal fluid

被引:32
作者
Bastos, Paulo [1 ,2 ]
Ferreira, Rita [3 ]
Manadas, Bruno [4 ]
Moreira, Paula I. [4 ,5 ]
Vitorino, Rui [2 ,6 ]
机构
[1] Univ Aveiro, Dept Chem, Aveiro, Portugal
[2] Univ Aveiro, Inst Biomed iBiMED, Dept Med Sci, Aveiro, Portugal
[3] Univ Aveiro, Dept Chem, QOPNA, Aveiro, Portugal
[4] Univ Coimbra, Ctr Neurosci & Cell Biol, CNC, Coimbra, Portugal
[5] Univ Coimbra, Fac Med, Lab Physiol, Coimbra, Portugal
[6] Univ Porto, Unidade Invest Cardiovasc, Fac Med, Dept Cirurgia & Fisiol, Oporto, Portugal
关键词
Cerebrospinal fluid; proteome; peptidomics; central nervous system; biological fluids; AMYOTROPHIC-LATERAL-SCLEROSIS; EXOSOME-MEDIATED TRANSFER; CENTRAL-NERVOUS-SYSTEM; ANTERIOR HORN NEURONS; ALZHEIMERS-DISEASE; MULTIPLE-SCLEROSIS; PARKINSONS-DISEASE; APOLIPOPROTEIN-E; ALPHA-SYNUCLEIN; AMYLOID-BETA;
D O I
10.1080/10408363.2017.1299682
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Cerebrospinal fluid (CSF) is an excellent source of biological information regarding the nervous system, once it is in close contact and accurately reflects alterations in this system. Several studies have analyzed differential protein profiles of CSF samples between healthy and diseased human subjects. However, the pathophysiological mechanisms and how CSF proteins relate to diseases are still poorly known. By applying bioinformatics tools, we attempted to provide new insights on the biological and functional meaning of proteomics data envisioning the identification of putative disease biomarkers. Bioinformatics analysis of data retrieved from 99 mass spectrometry (MS)-based studies on CSF profiling highlighted 1985 differentially expressed proteins across 49 diseases. A large percentage of the modulated proteins originate from exosome vesicles, and the majority are involved in either neuronal cell growth, development, maturation, migration, or neurotransmitter-mediated cellular communication. Nevertheless, some diseases present a unique CSF proteome profile, which were critically analyzed in the present study. For instance, 48 proteins were found exclusively upregulated in the CSF of patients with Alzheimer's disease and are mainly involved in steroid esterification and protein activation cascade processes. A higher number of exclusively upregulated proteins were found in the CSF of patients with multiple sclerosis (76 proteins) and with bacterial meningitis (70 proteins). Whereas in multiple sclerosis, these proteins are mostly involved in the regulation of RNA metabolism and apoptosis, in bacterial meningitis the exclusively upregulated proteins participate in inflammation and antibacterial humoral response, reflecting disease pathogenesis. The exploration of the contribution of exclusively upregulated proteins to disease pathogenesis will certainly help to envision potential biomarkers in the CSF for the clinical management of nervous system diseases.
引用
收藏
页码:185 / 204
页数:20
相关论文
共 204 条
[51]   Plasma and Cerebrospinal Proteomes From Children With Cerebral Malaria Differ From Those of Children With Other Encephalopathies [J].
Gitau, Evelyn N. ;
Kokwaro, Gilbert O. ;
Karanja, Henry ;
Newton, Charles R. J. C. ;
Ward, Stephen A. .
JOURNAL OF INFECTIOUS DISEASES, 2013, 208 (09) :1494-1503
[52]   Cerebrospinal fluid biomarkers of central catecholamine deficiency in Parkinson's disease and other synucleinopathies [J].
Goldstein, David S. ;
Holmes, Courtney ;
Sharabi, Yehonatan .
BRAIN, 2012, 135 :1900-1913
[53]   Sez-6 proteins affect dendritic arborization patterns and excitability of cortical pyramidal neurons [J].
Gunnersen, Jenny M. ;
Kim, Mary H. ;
Fuller, Stephanie J. ;
De Silva, Melanie ;
Britto, Joanne M. ;
Hammond, Vicki E. ;
Davies, Philip J. ;
Petrou, Steve ;
Faber, E. S. Louise ;
Sah, Pankaj ;
Tan, Seong-Seng .
NEURON, 2007, 56 (04) :621-639
[54]   Cystatin C in Cerebrospinal Fluid is Upregulated in Elderly Patients With Chronic Osteoarthritis Pain and Modulated Through Matrix Metalloproteinase 9-Specific Pathway [J].
Guo, Shu-Lin ;
Han, Cheng-Ta ;
Jung, Jiun-Lung ;
Chen, Wei-Jung ;
Mei, John Jian-Feng ;
Lee, Hoong-Chien ;
Cheng, Yu-Che .
CLINICAL JOURNAL OF PAIN, 2014, 30 (04) :331-339
[55]  
Hale John E., 2008, V425, P53, DOI 10.1007/978-1-60327-210-0_5
[56]   Nervous System Lyme Disease [J].
Halperin, John J. .
INFECTIOUS DISEASE CLINICS OF NORTH AMERICA, 2015, 29 (02) :241-+
[57]   The FAM3 superfamily member ILEI ameliorates Alzheimer's disease-like pathology by destabilizing the penultimate amyloid-β precursor [J].
Hasegawa, Hiroshi ;
Liu, Lei ;
Tooyama, Ikuo ;
Murayama, Shigeo ;
Nishimura, Masaki .
NATURE COMMUNICATIONS, 2014, 5
[58]   High Resolution Discovery Proteomics Reveals Candidate Disease Progression Markers of Alzheimer's Disease in Human Cerebrospinal Fluid [J].
Hendrickson, Ronald C. ;
Lee, Anita Y. H. ;
Song, Qinghua ;
Liaw, Andy ;
Wiener, Matt ;
Paweletz, Cloud P. ;
Seeburger, Jeffrey L. ;
Li, Jenny ;
Meng, Fanyu ;
Deyanova, Ekaterina G. ;
Mazur, Matthew T. ;
Settlage, Robert E. ;
Zhao, Xuemei ;
Southwick, Katie ;
Du, Yi ;
Holder, Dan ;
Sachs, Jeffrey R. ;
Laterza, Omar F. ;
Dallob, Aimee ;
Chappell, Derek L. ;
Snyder, Karen ;
Modur, Vijay ;
King, Elizabeth ;
Joachim, Catharine ;
Bondarenko, Andrey Y. ;
Shearman, Mark ;
Soper, Keith A. ;
Smith, David ;
Potter, William Z. ;
Koblan, Ken S. ;
Sachs, Alan B. ;
Yates, Nathan A. .
PLOS ONE, 2015, 10 (08)
[59]   Structural and Functional Analysis of Human Liver-Expressed Antimicrobial Peptide 2 [J].
Henriques, Sonia Troeira ;
Tan, Chia Chia ;
Craik, David J. ;
Clark, Richard J. .
CHEMBIOCHEM, 2010, 11 (15) :2148-2157
[60]   Changes in cerebrospinal fluid and blood plasma levels of IGF-II and its binding proteins in Alzheimer's disease: an observational study [J].
Hertze, Joakim ;
Nagga, Katarina ;
Minthon, Lennart ;
Hansson, Oskar .
BMC NEUROLOGY, 2014, 14