Gajda Angela M, Storch Judith
Department of Nutritional Sciences and Rutgers Center for Lipid Research Rutgers University, New Brunswick, NJ 08901, USA.
Department of Nutritional Sciences and Rutgers Center for Lipid Research Rutgers University, New Brunswick, NJ 08901, USA.
Prostaglandins Leukot Essent Fatty Acids. 2015 Feb;93:9-16. doi: 10.1016/j.plefa.2014.10.001. Epub 2014 Oct 14.
Fatty acid-binding proteins (FABP) are highly abundant cytosolic proteins that are expressed in most mammalian tissues. In the intestinal enterocyte, both liver- (LFABP; FABP1) and intestinal FABPs (IFABP; FABP2) are expressed. These proteins display high-affinity binding for long-chain fatty acids (FA) and other hydrophobic ligands; thus, they are believed to be involved with uptake and trafficking of lipids in the intestine. In vitro studies have identified differences in ligand-binding stoichiometry and specificity, and in mechanisms of FA transfer to membranes, and it has been hypothesized that LFABP and IFABP have different functions in the enterocyte. Studies directly comparing LFABP- and IFABP-null mice have revealed markedly different phenotypes, indicating that these proteins indeed have different functions in intestinal lipid metabolism and whole body energy homeostasis. In this review, we discuss the evolving knowledge of the functions of LFABP and IFABP in the intestinal enterocyte.
脂肪酸结合蛋白(FABP)是在大多数哺乳动物组织中大量表达的胞质蛋白。在肠道肠上皮细胞中,肝脏型脂肪酸结合蛋白(LFABP;FABP1)和肠道脂肪酸结合蛋白(IFABP;FABP2)均有表达。这些蛋白对长链脂肪酸(FA)和其他疏水性配体具有高亲和力结合;因此,它们被认为参与了肠道中脂质的摄取和转运。体外研究已经确定了配体结合化学计量和特异性以及脂肪酸转移至膜的机制方面的差异,并且有人推测LFABP和IFABP在肠上皮细胞中具有不同的功能。直接比较LFABP基因敲除小鼠和IFABP基因敲除小鼠的研究揭示了明显不同的表型,表明这些蛋白在肠道脂质代谢和全身能量稳态中确实具有不同的功能。在这篇综述中,我们讨论了关于LFABP和IFABP在肠道肠上皮细胞中功能的不断发展的知识。