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水通道蛋白4参与星形胶质细胞迁移和胶质瘢痕形成。

Involvement of aquaporin-4 in astroglial cell migration and glial scar formation.

作者信息

Saadoun Samira, Papadopoulos Marios C, Watanabe Hiroyuki, Yan Donghong, Manley Geoffrey T, Verkman A S

机构信息

Department of Medicine, Cardiovascular Research Institute, University of California, 505 Parnassus Avenue, San Francisco, CA 94143-0521, USA.

出版信息

J Cell Sci. 2005 Dec 15;118(Pt 24):5691-8. doi: 10.1242/jcs.02680. Epub 2005 Nov 22.

Abstract

Aquaporin-4, the major water-selective channel in astroglia throughout the central nervous system, facilitates water movement into and out of the brain. Here, we identify a novel role for aquaporin-4 in astroglial cell migration, as occurs during glial scar formation. Astroglia cultured from the neocortex of aquaporin-4-null mice had similar morphology, proliferation and adhesion, but markedly impaired migration determined by Transwell migration efficiency (18+/-2 vs 58+/-4% of cells migrated towards 10% serum in 8 hours; P<0.001) and wound healing rate (4.6 vs 7.0 microm/hour speed of wound edge; P<0.001) compared with wild-type mice. Transwell migration was similarly impaired (25+/-4% migrated cells) in wild-type astroglia after approximately 90% reduction in aquaporin-4 protein expression by RNA inhibition. Aquaporin-4 was polarized to the leading edge of the plasma membrane in migrating wild-type astroglia, where rapid shape changes were seen by video microscopy. Astroglial cell migration was enhanced by a small extracellular osmotic gradient, suggesting that aquaporin-4 facilitates water influx across the leading edge of a migrating cell. In an in vivo model of reactive gliosis and astroglial cell migration produced by cortical stab injury, glial scar formation was remarkably impaired in aquaporin-4-null mice, with reduced migration of reactive astroglia towards the site of injury. Our findings provide evidence for the involvement of aquaporin-4 in astroglial cell migration, which occurs during glial scar formation in brain injury, stroke, tumor and focal abscess.

摘要

水通道蛋白4是整个中枢神经系统星形胶质细胞中主要的水选择性通道,它促进水进出大脑。在此,我们发现水通道蛋白4在星形胶质细胞迁移中具有新的作用,这种作用在胶质瘢痕形成过程中会出现。从水通道蛋白4基因敲除小鼠的新皮质培养的星形胶质细胞具有相似的形态、增殖和黏附能力,但通过Transwell迁移效率(8小时内迁移至10%血清的细胞比例为18±2%,而野生型小鼠为58±4%;P<0.001)和伤口愈合率(伤口边缘移动速度为4.6微米/小时,而野生型小鼠为7.0微米/小时;P<0.001)测定,其迁移能力明显受损。通过RNA抑制使水通道蛋白4蛋白表达降低约90%后,野生型星形胶质细胞的Transwell迁移能力同样受损(迁移细胞比例为25±4%)。在迁移的野生型星形胶质细胞中,水通道蛋白4定位于质膜的前缘,通过视频显微镜可观察到此处有快速的形态变化。小的细胞外渗透梯度可增强星形胶质细胞的迁移,这表明水通道蛋白4促进水流入迁移细胞的前缘。在由皮质刺伤损伤产生的反应性胶质增生和星形胶质细胞迁移的体内模型中,水通道蛋白4基因敲除小鼠的胶质瘢痕形成明显受损,反应性星形胶质细胞向损伤部位的迁移减少。我们的研究结果为水通道蛋白4参与星形胶质细胞迁移提供了证据,这种迁移发生在脑损伤、中风、肿瘤和局灶性脓肿的胶质瘢痕形成过程中。

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