دورية أكاديمية

MMP7 cleaves remyelination-impairing fibronectin aggregates and its expression is reduced in chronic multiple sclerosis lesions

التفاصيل البيبلوغرافية
العنوان: MMP7 cleaves remyelination-impairing fibronectin aggregates and its expression is reduced in chronic multiple sclerosis lesions
المؤلفون: Wang, Peng, Gorter, Rianne P, de Jonge, Jenny C, Nazmuddin, Muhammad, Zhao, Chao, Amor, Sandra, Hoekstra, Dick, Baron, Wia
المصدر: Wang , P , Gorter , R P , de Jonge , J C , Nazmuddin , M , Zhao , C , Amor , S , Hoekstra , D & Baron , W 2018 , ' MMP7 cleaves remyelination-impairing fibronectin aggregates and its expression is reduced in chronic multiple sclerosis lesions ' , Glia , vol. 66 , no. 8 , pp. 1625-1643 . https://doi.org/10.1002/glia.23328Test
سنة النشر: 2018
المجموعة: University of Groningen research database
مصطلحات موضوعية: fibronectin aggregates, macrophage, microglia, MMP7, multiple sclerosis, CENTRAL-NERVOUS-SYSTEM, EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS, OLIGODENDROCYTE PROGENITOR MATURATION, MATRIX-METALLOPROTEINASE EXPRESSION, MYELIN MEMBRANE FORMATION, INDUCED DEMYELINATION, CNS REMYELINATION, RAFT-ASSOCIATION, EXTRA DOMAIN, DIFFERENTIATION
الوصف: Upon demyelination, transient expression of fibronectin precedes successful remyelination. However, in chronic demyelination observed in multiple sclerosis (MS), aggregates of fibronectin persist and contribute to remyelination failure. Accordingly, removing fibronectin (aggregates) would constitute an effective strategy for promoting remyelination. Matrix metalloproteinases (MMPs) are enzymes known to remodel extracellular matrix components, including fibronectin. Here, we examined the ability of MMPs to degrade fibronectin aggregates. Our findings reveal that MMP7 cleaved fibronectin aggregates resulting into a prominent 13kDa EIIIA (16kDa EDA)-containing fragment. MMP7 was upregulated during lysolecithin-induced demyelination, indicating its potential for endogenous fibronectin clearance. In contrast, the expression of proMMP7 was substantially decreased in chronic active and inactive MS lesions compared with control white matter and remyelinated MS lesions. Microglia and macrophages were major cellular sources of proMMP7 and IL-4-activated, but not IFN+LPS-activated, microglia and macrophages secreted significant levels of proMMP7. Also, conditioned medium of IL-4-activated macrophages most efficiently cleaved fibronectin aggregates upon MMP-activating conditions. Yet, coatings of MMP7-cleaved fibronectin aggregate fragments inhibited oligodendrocyte maturation, indicating that further degradation and/or clearance by phagocytosis is essential. These findings suggest that MMP7 cleaves fibronectin aggregates, while reduced (pro)MMP7 levels in MS lesions contribute to their persistent presence. Therefore, upregulating MMP7 levels may be key to remove remyelination-impairing fibronectin aggregates in MS lesions.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
العلاقة: https://research.rug.nl/en/publications/a24ff773-8500-4191-8116-3073fbee92fbTest
DOI: 10.1002/glia.23328
الإتاحة: https://doi.org/10.1002/glia.23328Test
https://hdl.handle.net/11370/a24ff773-8500-4191-8116-3073fbee92fbTest
https://research.rug.nl/en/publications/a24ff773-8500-4191-8116-3073fbee92fbTest
https://pure.rug.nl/ws/files/56664970/Wang_et_al_2017_Glia.pdfTest
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.CAC5CCCA
قاعدة البيانات: BASE