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多唾液酸转移酶ST8SiaIV的表达:多唾液酸化在体外干扰PC12细胞的黏附。

Expression of the polysialyltransferase ST8SiaIV: polysialylation interferes with adhesion of PC12 cells in vitro.

作者信息

Horstkorte R, Lessner N, Gerardy-Schahn R, Lucka L, Danker K, Reutter W

机构信息

Institut für Molekularbiologie und Biochemie, Freie Universität Berlin, Arnimallee 22, Berlin-Dahlem, D-14195, Germany.

出版信息

Exp Cell Res. 1999 Jan 10;246(1):122-8. doi: 10.1006/excr.1998.4255.

Abstract

Addition of polysialic acid (PSA) to the neural cell adhesion molecule, NCAM, represents a unique posttranslational modification. Polysialylation of NCAM is developmentally regulated and associated with neural regeneration and plastic processes, as well as learning and memory. Two enzymes, the polysialyltransferases ST8SiaII and ST8SiaIV, are known to be involved in the polysialylation of NCAM. Both enzymes are individually capable of catalyzing polysialylation of NCAM, but their time of occurrence and their tissue expression are different. In this study the influence of polysialylation on the nerve growth factor-induced differentiation of PC12 cells was investigated. For this purpose, PC12 cells, which endogenously express NCAM, were transfected with ST8SiaIV to produce, for the first time, a stable polysialylated PC12 cell. We demonstrate that integrin-dependent adhesion to collagen I is reduced in PSA-expressing PC12 cells. Furthermore, polysialylated cell membranes as matrix are a poor substrate for the adhesion and differentiation of PC12 cells, compared with normal cell membranes.

摘要

在神经细胞黏附分子(NCAM)上添加多唾液酸(PSA)代表了一种独特的翻译后修饰。NCAM的多唾液酸化受发育调控,并与神经再生和可塑性过程以及学习和记忆相关。已知两种酶,即多唾液酸转移酶ST8SiaII和ST8SiaIV,参与NCAM的多唾液酸化。这两种酶各自都能够催化NCAM的多唾液酸化,但它们出现的时间和组织表达有所不同。在本研究中,研究了多唾液酸化对神经生长因子诱导的PC12细胞分化的影响。为此,将内源性表达NCAM的PC12细胞用ST8SiaIV转染,首次产生稳定的多唾液酸化PC12细胞。我们证明,表达PSA的PC12细胞中依赖整合素的对I型胶原的黏附减少。此外,与正常细胞膜相比,多唾液酸化的细胞膜作为基质对PC12细胞的黏附和分化而言是较差的底物。

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