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一种新型血管生成诱导剂——分泌型β1,6-N-乙酰葡糖胺基转移酶V(GnT-V)受γ-分泌酶调控。

A secreted type of beta1,6 N-acetylglucosaminyltransferase V (GnT-V), a novel angiogenesis inducer, is regulated by gamma-secretase.

作者信息

Nakahara Susumu, Saito Takashi, Kondo Nami, Moriwaki Kenta, Noda Katsuhisa, Ihara Shinji, Takahashi Motoko, Ide Yoshihito, Gu Jianguo, Inohara Hidenori, Katayama Taiichi, Tohyama Masaya, Kubo Takeshi, Taniguchi Naoyuki, Miyoshi Eiji

机构信息

Department of Biochemistry, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan.

出版信息

FASEB J. 2006 Dec;20(14):2451-9. doi: 10.1096/fj.05-5066com.

Abstract

Glycosyltransferases are present in the Golgi apparatus in a membrane-bound form and are released from cells after cleavage by certain proteases. Beta1,6-N-acetylglucosaminyltransferase V (GnT-V), which is cleaved and secreted from the cells, is involved in the biosynthesis of beta1-6GlcNAc branching on N-glycans and has been implicated in tumor progression and metastasis. We recently reported that a secreted type of GnT-V (soluble GnT-V) itself could promote angiogenesis, which is completely different from its original function as a glycosyltransferase, and this might play a role in tumor invasion. In this study, to explore the molecular basis for this functional glycosyltransferase secretion, its cleavage site was examined and the protease(s) involved in that cleavage were identified. The NH2-terminal protein sequence of purified soluble GnT-V (approximately 100 kDa) from GnT-V-overexpressed cells revealed that its terminus started at His31, located at the boundary position between the transmembrane and stem regions. This secretion was not inhibited by a single amino acid mutation at the cleavage site (Leu29, Leu30 to Asp, His31 to Ala), but specifically inhibited by addition of DFK-167, a gamma-secretase inhibitor, suggesting that gamma-secretase is a plausible protease for secretion processing. In addition, transfection of the gene of familial Alzheimer's disease (FAD)[corrected]-linked presenilin-1, a component of gamma-secretase, increased the secretion rate of endogenous GnT-V; the secretion of soluble GnT-V (approximately 100 kDa) was completely inhibited in presenilin-1/2 double-deficient cells, which have no gamma-secretase activity. Collectively, these results demonstrate that Golgi-resident GnT-V is cleaved at the transmembrane region by gamma-secretase, and this might control tumor angiogenesis through a novel pathway.

摘要

糖基转移酶以膜结合形式存在于高尔基体中,并在被某些蛋白酶切割后从细胞中释放出来。β1,6-N-乙酰葡糖胺基转移酶V(GnT-V)从细胞中被切割并分泌出来,参与N-聚糖上β1-6GlcNAc分支的生物合成,并与肿瘤进展和转移有关。我们最近报道,一种分泌型的GnT-V(可溶性GnT-V)本身可以促进血管生成,这与其作为糖基转移酶的原始功能完全不同,并且这可能在肿瘤侵袭中起作用。在本研究中,为了探索这种功能性糖基转移酶分泌的分子基础,我们检查了其切割位点并鉴定了参与该切割的蛋白酶。从GnT-V过表达细胞中纯化的可溶性GnT-V(约100 kDa)的NH2末端蛋白质序列显示,其末端始于His31,位于跨膜区和茎区之间的边界位置。这种分泌不受切割位点(Leu29、Leu30突变为Asp,His31突变为Ala)的单个氨基酸突变的抑制,但通过添加γ-分泌酶抑制剂DFK-167受到特异性抑制,这表明γ-分泌酶是分泌加工的一种可能的蛋白酶。此外,转染家族性阿尔茨海默病(FAD)[已校正]-相关的早老素-1(γ-分泌酶的一个组成部分)的基因增加了内源性GnT-V的分泌率;在没有γ-分泌酶活性的早老素-1/2双缺陷细胞中,可溶性GnT-V(约100 kDa)的分泌被完全抑制。总体而言,这些结果表明,高尔基体驻留的GnT-V在跨膜区被γ-分泌酶切割,这可能通过一条新途径控制肿瘤血管生成。

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