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透明质酸的产生增强了细胞膜衍生的微泡的脱落。

Hyaluronan production enhances shedding of plasma membrane-derived microvesicles.

机构信息

Institutes of Biomedicine, Dentistry, and Biocenter Kuopio and Cancer Center of the University of Eastern Finland, P.O.B. 1627, FIN-70211 Kuopio, Finland.

Institutes of Biomedicine, Dentistry, and Biocenter Kuopio and Cancer Center of the University of Eastern Finland, P.O.B. 1627, FIN-70211 Kuopio, Finland.

出版信息

Exp Cell Res. 2013 Aug 1;319(13):2006-2018. doi: 10.1016/j.yexcr.2013.05.021. Epub 2013 Jun 1.

DOI:10.1016/j.yexcr.2013.05.021
PMID:23732660
Abstract

Many cell types secrete plasma membrane-bound microvesicles, suggested to play an important role in tissue morphogenesis, wound healing, and cancer spreading. However, the mechanisms of their formation have remained largely unknown. It was found that the tips of long microvilli induced in cells by overexpression of hyaluronan synthase 3 (HAS3) were detach into the culture medium as microvesicles. Moreover, several cell types with naturally active hyaluronan synthesis released high numbers of plasma membrane-derived vesicles, and inhibition of hyaluronan synthesis reduced their formation. The vesicles contained HAS, and were covered with a thick hyaluronan coat, a part of which was retained even after purification with high-speed centrifugation. HAS3 overexpressing MDCK cells cultured in a 3-D matrix as epithelial cysts released large amounts of HAS- and hyaluronan-positive vesicles from their basal surfaces into the extracellular matrix. As far as we know, hyaluronan synthesis is one of the first molecular mechanisms shown to stimulate the production of microvesicles. The microvesicles have a potential to deliver the hyaluronan synthase machinery and membrane and cytoplasmic materials to other cells, influencing tissue regeneration, inflammation and tumor progression.

摘要

许多细胞类型分泌质膜结合的微囊泡,被认为在组织形态发生、伤口愈合和癌症转移中发挥重要作用。然而,其形成的机制在很大程度上仍然未知。研究发现,通过过表达透明质酸合酶 3 (HAS3),细胞中长微绒毛的尖端会脱落到培养基中形成微囊泡。此外,几种具有天然活跃透明质酸合成的细胞类型释放大量的质膜衍生囊泡,而透明质酸合成的抑制减少了它们的形成。这些囊泡含有 HAS,并覆盖有一层厚厚的透明质酸涂层,其中一部分甚至在高速离心纯化后仍保留。在 3-D 基质中培养的过表达 HAS3 的 MDCK 细胞从基底表面向细胞外基质释放大量 HAS 和透明质酸阳性囊泡。据我们所知,透明质酸合成是第一个被证明能刺激微囊泡产生的分子机制之一。这些微囊泡有可能将透明质酸合酶机制以及膜和细胞质物质输送到其他细胞,影响组织再生、炎症和肿瘤进展。

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