| Literature DB >> 27830502 |
William S Blaner1, Yang Li2, Pierre-Jacques Brun2, Jason J Yuen2, Seung-Ah Lee2, Robin D Clugston2.
Abstract
It is well established that chylomicron remnant (dietary) vitamin A is taken up from the circulation by hepatocytes, but more than 80 % of the vitamin A in the liver is stored in hepatic stellate cells (HSC). It presently is not known how vitamin A is transferred from hepatocytes to HSCs for storage. Since retinol-binding protein 4 (RBP4), a protein that is required for mobilizing stored vitamin A, is synthesized solely by hepatocytes and not HSCs, it similarly is not known how vitamin A is transferred from HSCs to hepatocytes. Although it has long been thought that RBP4 is absolutely essential for delivering vitamin A to tissues, recent research has proven that this notion is incorrect since total RBP4-deficiency is not lethal. In addition to RBP4, vitamin A is also found in the circulation bound to lipoproteins and as retinoic acid bound to albumin. It is not known how these different circulating pools of vitamin A contribute to the vitamin A needs of different tissues. In our view, better insight into these three issues is required to better understand vitamin A absorption, storage and mobilization. Here, we provide an up to date synthesis of current knowledge regarding the intestinal uptake of dietary vitamin A, the storage of vitamin A within the liver, and the mobilization of hepatic vitamin A stores, and summarize areas where our understanding of these processes is incomplete.Entities:
Keywords: Adipose tissue; Chylomicrons; Hepatic stellate cells; RBP4; Retinoid; Retinyl ester storage; Vitamin A
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Year: 2016 PMID: 27830502 DOI: 10.1007/978-94-024-0945-1_4
Source DB: PubMed Journal: Subcell Biochem ISSN: 0306-0225