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Injured astrocytes are repaired by Synaptotagmin XI-regulated lysosome exocytosis

机译:突触结合蛋白XI调节溶酶体胞吐作用修复受损的星形胶质细胞

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Astrocytes are known to facilitate repair following brain injury; however, little is known about how injured astrocytes repair themselves. Repair of cell membrane injury requires Ca2+-triggered vesicle exocytosis. In astrocytes, lysosomes are the main Ca2+-regulated exocytic vesicles. Here we show that astrocyte cell membrane injury results in a large and rapid calcium increase. This triggers robust lysosome exocytosis where the fusing lysosomes release all luminal contents and merge fully with the plasma membrane. In contrast to this, receptor stimulation produces a small sustained calcium increase, which is associated with partial release of the lysosomal luminal content, and the lysosome membrane does not merge into the plasma membrane. In most cells, lysosomes express the synaptotagmin (Syt) isoform Syt VII; however, this isoform is not present on astrocyte lysosomes and exogenous expression of Syt VII on lysosome inhibits their exocytosis. Deletion of one of the most abundant Syt isoform in astrocyte - Syt XI - suppresses astrocyte lysosome exocytosis. This identifies lysosome as Syt XI-regulated exocytic vesicle in astrocytes. Further, inhibition of lysosome exocytosis (by Syt XI depletion or Syt VII expression) prevents repair of injured astrocytes. These results identify the lysosomes and Syt XI as the sub-cellular and molecular regulators, respectively of astrocyte cell membrane repair.
机译:已知星形胶质细胞可促进脑损伤后的修复。然而,关于受损星形胶质细胞如何自我修复的了解甚少。修复细胞膜损伤需要触发Ca2 +触发的囊泡胞吐作用。在星形胶质细胞中,溶酶体是Ca2 +调节的主要囊泡。在这里,我们表明星形胶质细胞膜损伤导致钙大量快速增加。这触发了强大的溶酶体胞吐作用,其中融合的溶酶体释放出所有腔内物质并与质膜完全融合。与此相反,受体刺激产生少量持续的钙增加,这与溶酶体腔内含物的部分释放有关,并且溶酶体膜不会融合到质膜中。在大多数细胞中,溶酶体表达突触标签蛋白(Syt)同工型Syt VII。然而,这种同种型在星形胶质细胞溶酶体上不存在,Syt VII在溶酶体上的外源表达抑制了它们的胞吐作用。删除星形胶质细胞中最丰富的Syt同工型之一-Syt XI可抑制星形胶质细胞溶酶体的胞吐作用。这将溶酶体鉴定为星形胶质细胞中Syt XI调节的囊泡。此外,溶酶体胞吐作用的抑制(通过Syt XI耗竭或Syt VII表达)可防止受损星形胶质细胞的修复。这些结果确定溶酶体和Syt XI分别是星形胶质细胞膜修复的亚细胞和分子调节剂。

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