Department of Cell Biology and Morphology, Akita University Graduate School of Medicine, 1-1-1 Hondo, Akita 010-8543, Japan.
Med Hypotheses. 2013 Aug;81(2):222-4. doi: 10.1016/j.mehy.2013.04.045. Epub 2013 May 17.
Hepatic stellate cells (HSCs), also known as Ito cells, fat-storing cells, vitamin A-storing cells or lipocytes, reside in the spaces between hepatocytes and liver sinusoids. Vitamin A storage within the HSCs is achieved through the cooperative action of two proteins, cellular retinol-binding protein (CRBP) I and lecithin:retinol acyltransferase (LRAT). After the discovery that HSCs are responsible not only for the storage of vitamin A, but also for the development of liver fibrosis and subsequent liver cirrhosis, HSCs have been considered a therapeutic target for prevention or reversal of liver fibrogenesis. We have reported that HSCs acquire retinoid responsiveness after in vitro activation by post-transcriptional upregulation of retinoic acid receptor α gene expression. Here we extend this observation in relation to the functions of CRBP I and LRAT, and propose a hypothesis that increased retinoid signaling in activated HSCs forms a feedback loop toward vitamin A restoration in the liver.
肝星状细胞(HSCs),又称 Ito 细胞、脂肪储存细胞、维生素 A 储存细胞或脂细胞,位于肝细胞和肝窦之间的间隙中。HSCs 内的维生素 A 储存是通过两种蛋白质的协同作用实现的,即细胞视黄醇结合蛋白(CRBP)I 和卵磷脂:视黄醇酰基转移酶(LRAT)。在发现 HSCs 不仅负责储存维生素 A,还负责肝纤维化的发展和随后的肝硬化之后,HSCs 已被认为是预防或逆转肝纤维化的治疗靶点。我们已经报道,HSCs 在体外通过转录后上调维甲酸受体 α 基因表达而被激活后获得视黄酸反应性。在这里,我们将这一观察结果扩展到 CRBP I 和 LRAT 的功能上,并提出了一个假设,即激活的 HSCs 中增加的视黄酸信号形成了一个反馈回路,有助于肝脏中维生素 A 的恢复。