de Duve Institute, Université Catholique de Louvain, Brussels, Belgium.
Gastroenterology. 2011 Oct;141(4):1432-8, 1438.e1-4. doi: 10.1053/j.gastro.2011.06.049. Epub 2011 Jun 25.
BACKGROUND& AIMS: Embryonic biliary precursor cells form a periportal sheet called the ductal plate, which is progressively remodeled to generate intrahepatic bile ducts. A limited number of ductal plate cells participate in duct formation; those not involved in duct development are believed to involute by apoptosis. Moreover, cells that express the SRY-related HMG box transcription factor 9 (SOX9), which include the embryonic ductal plate cells, were proposed to continuously supply the liver with hepatic cells. We investigated the role of the ductal plate in hepatic morphogenesis.
Apoptosis and proliferation were investigated by immunostaining of mouse and human fetal liver tissue. The postnatal progeny of SOX9-expressing ductal plate cells was analyzed after genetic labeling, at the ductal plate stage, by Cre-mediated recombination of a ROSA26RYFP reporter allele. Inducible Cre expression was induced by SOX9 regulatory regions, inserted in a bacterial artificial chromosome. Livers were studied from mice under normal conditions and during diet-induced regeneration.
Ductal plate cells did not undergo apoptosis and showed limited proliferation. They generated cholangiocytes lining interlobular bile ducts, bile ductules, and canals of Hering, as well as periportal hepatocytes. Oval cells that appeared during regeneration also derived from the ductal plate. We did not find that liver homeostasis required a continuous supply of cells from SOX9-expressing progenitors.
The ductal plate gives rise to cholangiocytes lining the intrahepatic bile ducts, including its most proximal segments. It also generates periportal hepatocytes and adult hepatic progenitor cells.
背景与目的:胚胎胆管前体细胞形成了一个被称为胆管板的门管区周围薄片,它逐渐重塑以生成肝内胆管。只有少数胆管板细胞参与胆管形成;那些未参与胆管发育的细胞被认为通过细胞凋亡而退化。此外,表达性染色体相关高迁移率族盒转录因子 9(SRY-related HMG box transcription factor 9,SOX9)的细胞,包括胚胎胆管板细胞,被认为持续为肝脏提供肝细胞。我们研究了胆管板在肝形态发生中的作用。
通过对小鼠和人胎肝组织进行免疫染色,研究了细胞凋亡和增殖情况。通过 Cre 介导的 ROSA26RYFP 报告基因等位基因重组,在胆管板阶段对 SOX9 表达的胆管板细胞进行遗传标记,分析其在出生后的后代。诱导型 Cre 表达是通过插入细菌人工染色体中的 SOX9 调控区来诱导的。在正常条件和饮食诱导再生期间,研究了小鼠的肝脏。
胆管板细胞不发生细胞凋亡,增殖有限。它们生成了胆管上皮细胞,包括小叶间胆管、胆管小管和 Hering 管,以及门管区周围的肝细胞。再生过程中出现的卵圆细胞也源自胆管板。我们没有发现肝脏的内稳态需要来自 SOX9 表达祖细胞的持续细胞供应。
胆管板产生了胆管上皮细胞,包括其最近端的部分。它还产生了门管区周围的肝细胞和成年肝祖细胞。