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首页> 外文期刊>Biochimica et Biophysica Acta. Molecular and cell biology of Lipids >Intestinal cholesterol absorption: identification of different binding proteins for cholesterol and cholesterol absorption inhibitors in the enterocyte brush border membrane
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Intestinal cholesterol absorption: identification of different binding proteins for cholesterol and cholesterol absorption inhibitors in the enterocyte brush border membrane

机译:肠道胆固醇吸收:在肠细胞刷状缘膜中鉴定出不同的胆固醇结合蛋白和胆固醇吸收抑制剂

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Absorption of cholesterol from the intestine is a central part of body cholesterol homeostasis. The molecular mechanisms of intestinal cholesterol absorption and the proteins mediating membrane transport are not known.We therefore aimed to identify the proteins involved in intestinal cholesterol absorption across the luminal brush border membrane of small intestinal enterocytes. By photoaffinity labeling using photoreactive derivatives of cholesterol and 2-azetidinone cholesterol absorption inhibitors, an kDa and a 145-kDa integral membrane protein were identified as specific binding proteins for cholesterol and cholesterol absorption inhibitors, respectively, in the brush border membrane of small intestinal enterocytes. The 80-kDa cholesterol-binding protein did not interact with cholesterol absorption inhibitors and vice versa; cholesterol or plant sterols did not interfere with the 145-kDa molecular target for cholesterol absorption inhibitors. Both proteins showed an identical tissue distribution and were exclusively found at the anatomical sites of cholesterol absorption-duodenum, jejunum and ileum. Neither stomach, cecum, colon, rectum, kidney, liver nor fat tissue expressed the 80-or 145-kDa binding proteins for cholesterol and cholesterol absorption inhibitors. Both proteins are different from the hitherto described candidate proteins for the intestinal cholesterol transporter, -SR-BI, ABC G5/ABC G8 or ABC Al. Our data strongly suggest that intestinal cholesterol absorption is not facilitated by a single transporter protein but occurs by a complexmachinery.Two specific binding proteins for cholesterol (80 kDa) and cholesterol absorption inhibitors (145 kDa) of the enterocyte brush border membrane are probable protein constituents of the mechanism responsible for the intestinal absorption of cholesterol.
机译:从肠道吸收胆固醇是体内胆固醇稳态的核心部分。肠胆固醇吸收的分子机制和介导膜转运的蛋白质尚不清楚,因此我们旨在鉴定参与小肠肠上皮细胞腔刷缘膜的肠胆固醇吸收的蛋白质。通过使用胆固醇和2-氮杂环丁酮胆固醇吸收抑制剂的光反应性衍生物进行光亲和标记,在小肠肠上皮细胞的刷状缘膜中,分别将kDa和145-kDa整合膜蛋白鉴定为胆固醇和胆固醇吸收抑制剂的特异性结合蛋白。 。 80 kDa的胆固醇结合蛋白不与胆固醇吸收抑制剂相互作用,反之亦然。胆固醇或植物固醇不会干扰145 kDa的胆固醇吸收抑制剂分子靶标。两种蛋白质均显示相同的组织分布,并且仅在胆固醇吸收十二指肠,空肠和回肠的解剖部位发现。胃,盲肠,结肠,直肠,肾脏,肝脏或脂肪组织均未表达80-或145-kDa的胆固醇和胆固醇吸收抑制剂结合蛋白。两种蛋白质均与迄今为止描述的用于肠胆固醇转运蛋白的候选蛋白质-SR-BI,ABC G5 / ABC G8或ABC Al不同。我们的数据强烈表明,肠道胆固醇的吸收不是由单个转运蛋白促进的,而是由复杂的机械实现的。肠细胞刷状缘膜的胆固醇(80 kDa)和胆固醇吸收抑制剂(145 kDa)的两种特异性结合蛋白可能是蛋白质成分肠道吸收胆固醇的机制。

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