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钴胺素(维生素B12)的受体介导内吞作用。

Receptor-mediated endocytosis of cobalamin (vitamin B12).

作者信息

Seetharam B

机构信息

Department of Medicine and Biochemistry, Medical College of Wisconsin, Milwaukee, USA.

出版信息

Annu Rev Nutr. 1999;19:173-95. doi: 10.1146/annurev.nutr.19.1.173.

Abstract

Dietary cobalamin (Cbl) (vitamin B12) is utilized as methyl-Cbl and the coenzyme 5'-deoxyadenosyl Cbl by cells of the body that have the enzymes methionine synthase and methyl malonyl CoA mutase, which convert homocysteine to methionine and methyl malonyl CoA to succinyl CoA, respectively. Prior to conversions and utilizations as the active alkyl forms of Cbl, dietary Cbl is absorbed and transported across cellular plasma membranes by two receptor-mediated events. First, dietary and biliary Cbl bound to gastric intrinsic factor (IF) presented apically to the ileal absorptive enterocytes is transported to the circulation by receptor-mediated endocytosis via apically expressed IF-Cbl receptor. Second, Cbl bound to plasma transcobalamin (TC) II is taken up from the circulation by all cells via a TC II receptor expressed in the plasma membrane of these cells, and in polarized cells via a TC II receptor expressed in the basolateral membranes. This review updates recent work and focuses on (a) the molecular and cellular aspects of Cbl binding protein ligands, IF and TC II, and their cell-surface receptors, IF-Cbl receptor and TC II receptor; (b) the cellular sorting pathways of internalized Cbl bound to IF and TC II in polarized epithelial cells; and (c) the absorption and transport disorders that cause Cbl deficiency.

摘要

膳食钴胺素(Cbl)(维生素B12)被体内具有甲硫氨酸合酶和甲基丙二酰辅酶A变位酶的细胞用作甲基钴胺素和辅酶5'-脱氧腺苷钴胺素,这两种酶分别将同型半胱氨酸转化为甲硫氨酸,将甲基丙二酰辅酶A转化为琥珀酰辅酶A。在转化并用作Cbl的活性烷基形式之前,膳食Cbl通过两个受体介导的过程被吸收并转运穿过细胞质膜。首先,与胃内因子(IF)结合的膳食和胆汁Cbl经顶端呈递给回肠吸收性肠上皮细胞,通过顶端表达的IF-Cbl受体经受体介导的内吞作用转运至循环系统。其次,与血浆转钴胺素(TC)II结合的Cbl被所有细胞通过这些细胞质膜上表达的TC II受体从循环系统摄取,在极化细胞中则通过基底外侧膜上表达的TC II受体摄取。本综述更新了近期的研究工作,并聚焦于:(a)Cbl结合蛋白配体、IF和TC II及其细胞表面受体(IF-Cbl受体和TC II受体)的分子和细胞层面;(b)极化上皮细胞中与IF和TC II结合的内化Cbl的细胞分选途径;以及(c)导致Cbl缺乏的吸收和转运障碍。

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