iTRAQ-based Quantitative Proteomic Analysis of Dural Tissues Reveals Upregulated Haptoglobin to be a Potential Biomarker of Moyamoya Disease

被引:2
作者
Zhang, Xiaojun [1 ]
Yin, Lin [2 ]
Jia, Xiaofang [2 ]
Zhang, Yujiao [2 ]
Liu, Tiefu [2 ]
Zhang, Lijun [2 ]
机构
[1] 85th Hosp Chinese Peoples Liberat Army, Shanghai 200052, Peoples R China
[2] Fudan Univ, Shanghai Publ Hlth Clin Ctr, 2901 Caolang Rd, Shanghai 201508, Peoples R China
关键词
Moyamoya disease; dura mater; proteomics; iTRAQ; haptoglobin; strokes; BLOOD BIOMARKERS; GROWTH-FACTOR; LABEL-FREE; PATHOGENESIS; MATER; VALIDATION; CAVEOLIN-1; EXPRESSION; DISCOVERY; PROTEINS;
D O I
10.2174/1570164617666191210103652
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Moyamoya Disease (MMD) is a rare cerebrovascular disease with a high rate of disability and mortality. Immune reactions have been implicated in the pathogenesis of MMD, however, the underlying mechanism is still unclear. Objective: To identify proteins related to MMD specially involved in the immunogenesis, we performed a proteomic study. Methods: In this work, dural tissues or plasma from 98 patients with MMD, 17 disease controls without MMD, and 12 healthy donors were included. Proteomic profiles of dural tissues from 4 MMD and 4 disease controls were analyzed by an isobaric tag for relative and absolute quantitation (iTRAQ)-based proteomics. The immune-related proteins were explored by bioinformatics and the key MMD-related proteins were verified by western blot, multiple reaction monitoring methods, enzyme-linked immunosorbent assay, and tissue microarray. Results: 1,120 proteins were identified, and 82 MMD-related proteins were found with more than 1.5 fold difference compared with those in the control samples. Gene Ontology analysis showed that 29 proteins were immune-related. In particular, Haptoglobin (HP) was up-regulated in dural tissue and plasma of MMD samples compared to the controls, and its up-regulation was found to be sex- and MMD Suzuki grade dependent. Through Receiver Operating Characteristic (ROC) analysis, HP can well discriminate MMD and healthy donors with the Area Under the Curve (AUC) of 0.953. Conclusion: We identified the biggest protein database of the dura mater. 29 out of 82 differentially expressed proteins in MMD are involved in the immune process. Of which, HP was up-regulated in dural tissue and plasma of MMD, with sex- and MMD Suzuki grade-dependence. HP might be a potential biomarker of MMD.
引用
收藏
页码:27 / 37
页数:11
相关论文
共 80 条
[1]   Novel and recurrent RNF213 variants in Japanese pediatric patients with moyamoya disease [J].
Akagawa H. ;
Mukawa M. ;
Nariai T. ;
Nomura S. ;
Aihara Y. ;
Onda H. ;
Yoneyama T. ;
Kudo T. ;
Sumita K. ;
Maehara T. ;
Kawamata T. ;
Kasuya H. .
Human Genome Variation, 5 (1)
[2]   Pachymeningeal enhancement-a comprehensive review of literature [J].
Antony, Joyce ;
Hacking, Craig ;
Jeffree, Rosalind L. .
NEUROSURGICAL REVIEW, 2015, 38 (04) :649-659
[3]   Identification of novel biomarker candidates by proteomic analysis of cerebrospinal fluid from patients with moyamoya disease using SELDI-TOF-MS [J].
Araki, Yoshio ;
Yoshikawa, Kazuhiro ;
Okamoto, Sho ;
Sumitomo, Masaki ;
Maruwaka, Mikio ;
Wakabayashi, Toshihiko .
BMC NEUROLOGY, 2010, 10
[4]   Novel epidemiological features of moyamoya disease [J].
Baba, T. ;
Houkin, K. ;
Kuroda, S. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2008, 79 (08) :900-904
[5]   Caveolin-1, Ring finger protein 213, and endothelial function in Moyamoya disease [J].
Bang, Oh Young ;
Chung, Jong-Won ;
Kim, Suk Jae ;
Oh, Mi Jeong ;
Kim, Soo Yoon ;
Cho, Yeon Hee ;
Cha, Jihoon ;
Yeon, Je Young ;
Kim, Keon Ha ;
Kim, Gyeong-Moon ;
Chung, Chin-Sang ;
Lee, Kwang Ho ;
Ki, Chang-Seok ;
Jeon, Pyoung ;
Kim, Jong-Soo ;
Hong, Seung Chyul ;
Moon, Gyeong Joon .
INTERNATIONAL JOURNAL OF STROKE, 2016, 11 (09) :999-1008
[6]   The Pathophysiology of Moyamoya Disease: An Update [J].
Bang, Oh Young ;
Fujimura, Miki ;
Kim, Seung-Ki .
JOURNAL OF STROKE, 2016, 18 (01) :12-20
[7]   Proteomic studies in the discovery of cerebrospinal fluid biomarkers for amyotrophic lateral sclerosis [J].
Barschke, Peggy ;
Oeckl, Patrick ;
Steinacker, Petra ;
Ludolph, Albert ;
Otto, Markus .
EXPERT REVIEW OF PROTEOMICS, 2017, 14 (09) :769-777
[8]   Vasculogenic and Angiogenic Pathways in Moyamoya Disease [J].
Bedini, Gloria ;
Blecharz, Kinga G. ;
Nava, Sara ;
Vajkoczy, Peter ;
Alessandri, Giulio ;
Ranieri, Michela ;
Acerbi, Francesco ;
Ferroli, Paolo ;
Riva, Daria ;
Esposito, Silvia ;
Pantaleoni, Chiara ;
Nardocci, Nardo ;
Zibordi, Federica ;
Ciceri, Elisa ;
Parati, Eugenio A. ;
Bersano, Anna .
CURRENT MEDICINAL CHEMISTRY, 2016, 23 (04) :315-345
[9]   Analysis and comparison of lignin peroxidases between fungi and bacteria using three different modes of Chou's general pseudo amino acid composition [J].
Behbahani, Mandana ;
Mohabatkar, Hassan ;
Nosrati, Mokhtar .
JOURNAL OF THEORETICAL BIOLOGY, 2016, 411 :1-5
[10]   Research Progresses in Understanding the Pathophysiology of Moyamoya Disease [J].
Bersano, Anna ;
Guey, Stephanie ;
Bedini, Gloria ;
Nava, Sara ;
Herve, Dominique ;
Vajkoczy, Peter ;
Tatlisumak, Turgut ;
Sareela, Marika ;
van der Zwan, Albert ;
Klijn, Catharina J. M. ;
Braun, Kees P. J. ;
Kronenburg, Annick ;
Acerbi, Francesco ;
Brown, Martin M. ;
Calviere, Lionel ;
Cordonnier, Charlotte ;
Henon, Hilde ;
Thines, Laurent ;
Khan, Nadia ;
Czabanka, M. ;
Kraemer, Markus ;
Simister, Robert ;
Prontera, Paolo ;
Tournier-Lasserve, E. ;
Parati, Eugenio .
CEREBROVASCULAR DISEASES, 2016, 41 (3-4) :105-118