Zhao Chao, Fancy Stephen P J, ffrench-Constant Charles, Franklin Robin J M
Department of Veterinary Medicine and Cambridge Centre for Brain Repair, University of Cambridge, Madingley Road, Cambridge CB3 0ES, UK.
Neurobiol Dis. 2008 Aug;31(2):209-17. doi: 10.1016/j.nbd.2008.04.007. Epub 2008 May 4.
Osteopontin (OPN) is a key immunoregulator in the autoimmune-mediated demyelinating disease multiple sclerosis. OPN may also play a role in the remyelination since it is 1) a ligand for alpha V integrins, several of which regulate the properties of the oligodendrocyte precursor cells (OPCs) primarily responsible for remyelination, and 2) enhances myelin membrane formation in OPC lines. Here we show that OPN is expressed at high levels during remyelination of toxin-induced demyelination. The increased expression is due to mRNA expression in macrophages and follows differences in macrophage responses to demyelination in young and old adult animals. To identify the role of OPN in remyelination focal demyelination was induced in wild-type and OPN(-/-) mice. There was no difference in the rate of remyelination between the two groups indicating that OPN is not a critical component of remyelination.
骨桥蛋白(OPN)是自身免疫介导的脱髓鞘疾病多发性硬化症中的关键免疫调节因子。OPN也可能在髓鞘再生中发挥作用,因为它:1)是αV整合素的配体,其中几种整合素调节主要负责髓鞘再生的少突胶质前体细胞(OPC)的特性;2)增强OPC系中的髓鞘膜形成。在此我们表明,在毒素诱导的脱髓鞘的髓鞘再生过程中,OPN高水平表达。表达增加是由于巨噬细胞中的mRNA表达,并且随年轻和成年老年动物中巨噬细胞对脱髓鞘反应的差异而变化。为了确定OPN在髓鞘再生中的作用,在野生型和OPN(-/-)小鼠中诱导局灶性脱髓鞘。两组之间的髓鞘再生速率没有差异,表明OPN不是髓鞘再生的关键组成部分。