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微原纤维相关糖蛋白MAGP-2刺激弹性纤维组装。

Microfibril-associated MAGP-2 stimulates elastic fiber assembly.

作者信息

Lemaire Raphael, Bayle Julie, Mecham Robert P, Lafyatis Robert

机构信息

Department of Medicine, Arthritis Center, Boston University School of Medicine, Boston, Massachusetts 02118, USA.

出版信息

J Biol Chem. 2007 Jan 5;282(1):800-8. doi: 10.1074/jbc.M609692200. Epub 2006 Nov 10.

Abstract

Elastic fibers are complex structures composed of a tropoelastin inner core and microfibril outer mantle guiding tropoelastin deposition. Microfibrillar proteins mainly include fibrillins and microfibril-associated glycoproteins (MAGPs). MAGP-2 exhibits developmental expression peaking at elastic fiber onset, suggesting that MAGP-2 mediates elastic fiber assembly. To determine whether MAGP-2 regulates elastic fiber assembly, we used an in vitro model featuring doxycycline-regulated cells conditionally overexpressing exogenous MAGP-2 and constitutively expressing enhanced green fluorescent protein-tagged tropoelastin. Analysis by immunofluorescent staining showed that MAGP-2 overexpression dramatically increased elastic fibers levels, independently of extracellular levels of soluble tropoelastin, indicating that MAGP-2 stimulates elastic fiber assembly. This was associated with increased levels of matrix-associated MAGP-2. Electron microscopy showed that MAGP-2 specifically associates with microfibrils and that elastin globules primarily colocalize with MAGP-2-associated microfibrils, suggesting that microfibril-associated MAGP-2 facilitates elastic fiber assembly. MAGP-2 overexpression did not change levels of matrix-associated fibrillin-1, MAGP-1, fibulin-2, fibulin-5, or emilin-1, suggesting that microfibrils and other elastic fiber-associated proteins known to regulate elastogenesis do not mediate MAGP-2-induced elastic fiber assembly. Moreover, mutation analysis showed that MAGP-2 does not stimulate elastic fiber assembly through its RGD motif, suggesting that integrin receptor binding does not mediate MAGP-2-induced elastic fiber assembly. Because MAGP-2 interacts with Jagged-1 that controls cell-matrix interaction and cell motility, two key factors in elastic fiber macroassembly, microfibril-associated MAGP-2 may stimulate elastic fiber macroassembly by targeting the release of elastin globules from the cell membrane onto developing elastic fibers.

摘要

弹性纤维是由原弹性蛋白内核和引导原弹性蛋白沉积的微原纤维外膜组成的复杂结构。微原纤维蛋白主要包括原纤蛋白和微原纤维相关糖蛋白(MAGPs)。MAGP - 2在弹性纤维开始形成时呈现发育性表达高峰,这表明MAGP - 2介导弹性纤维组装。为了确定MAGP - 2是否调节弹性纤维组装,我们使用了一种体外模型,该模型具有多西环素调控的细胞,可条件性过表达外源性MAGP - 2并组成性表达增强型绿色荧光蛋白标记的原弹性蛋白。免疫荧光染色分析表明,MAGP - 2过表达显著增加了弹性纤维水平,且与可溶性原弹性蛋白的细胞外水平无关,这表明MAGP - 2刺激弹性纤维组装。这与基质相关的MAGP - 2水平增加有关。电子显微镜显示,MAGP - 2特异性地与微原纤维结合,并且弹性蛋白小球主要与MAGP - 2相关的微原纤维共定位,这表明微原纤维相关的MAGP - 2促进弹性纤维组装。MAGP - 2过表达并未改变基质相关的原纤蛋白 - 1、MAGP - 1、纤连蛋白 - 2、纤连蛋白 - 5或埃米林 - 1的水平,这表明已知调节弹性生成的微原纤维和其他弹性纤维相关蛋白并不介导MAGP - 2诱导的弹性纤维组装。此外,突变分析表明,MAGP - 2不会通过其RGD基序刺激弹性纤维组装,这表明整合素受体结合并不介导MAGP - 2诱导的弹性纤维组装。由于MAGP - 2与控制细胞 - 基质相互作用和细胞运动性的Jagged - 1相互作用,而这两个因素是弹性纤维宏观组装的关键因素,因此微原纤维相关的MAGP - 2可能通过将弹性蛋白小球从细胞膜释放到正在发育的弹性纤维上,从而刺激弹性纤维宏观组装。

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