Koike T, Shiojiri N
Department of Biology, Faculty of Science, Shizuoka University, Japan.
Differentiation. 1996 Oct;61(1):35-43. doi: 10.1046/j.1432-0436.1996.6110035.x.
The differentiation of hepatic endodermal cells is affected by endodermal-mesodermal interactions. To examine the control mechanisms of this differentiation, we cultured mouse liver primordium and tissue recombinants of the hepatic endoderm with homo- or heterologous mesenchyme in vitro. When the hepatic primordia at somite stages 15-23 were cultured in vitro for 5-10 days, the endodermal cells differentiated into large hepatocytes expressing alpha-fetoprotein (AFP), albumin and carbamoylphosphate synthetase I (CPSI) and storing glycogen. AFP continued to be expressed in hepatocytes through culture for 10 days. Albumin and CPSI expression started in hepatocytes at 1 and 2 days after culture, respectively. Dexamethasone stimulated hepatocyte differentiation (expression of CPSI and glycogen accumulation) and large lumen formation of hepatocytes, but it did not change the commencement of differentiation. When the hepatic endoderm was recombined with hepatic mesenchyme or 4-day embryonic chick lung mesenchyme, clotted in Matrigel, which is a basement-membrane-like substratum, and cultured for 5 days in vitro, it differentiated into large hepatocytes expressing albumin and CPSI and accumulating glycogen. Lung mesenchyme promoted duct formation more efficiently than the hepatic mesenchyme did. However, the hepatic endodermal cells failed to differentiate into large hepatocytes when cultured with 6-day embryonic chick metanephric mesenchyme or with 2.5-day chick somitic mesenchyme, or cultured alone in Matrigel, suggesting that the endodermal cells require the presence of splanchnic mesoderm for their differentiation in vitro. Addition of HGF (hepatocyte growth factor), aFGF (acidic fibroblast growth factor), or bFGF (basic fibroblast growth factor) also did not support the survival of hepatic endodermal cells or hepatocyte differentiation in culture without mesenchyme. Matrigel and those growth factors might not be a suitable substitute for the mesenchyme.
肝内胚层细胞的分化受内胚层-中胚层相互作用的影响。为了研究这种分化的调控机制,我们在体外培养了小鼠肝原基以及肝内胚层与同源或异源间充质的组织重组体。当体节期15 - 23的肝原基在体外培养5 - 10天时,内胚层细胞分化为表达甲胎蛋白(AFP)、白蛋白和氨甲酰磷酸合成酶I(CPSI)并储存糖原的大肝细胞。在培养10天的过程中,AFP持续在肝细胞中表达。白蛋白和CPSI的表达分别在培养后第1天和第2天开始于肝细胞中。地塞米松刺激肝细胞分化(CPSI表达和糖原积累)以及肝细胞形成大的管腔,但它并没有改变分化的起始。当肝内胚层与肝间充质或4天胚胎期鸡肺间充质重组,在基底膜样基质Matrigel中凝结,并在体外培养5天时,它分化为表达白蛋白和CPSI并积累糖原的大肝细胞。肺间充质比肝间充质更有效地促进胆管形成。然而,当与6天胚胎期鸡后肾间充质或2.5天鸡体节间充质一起培养,或单独在Matrigel中培养时,肝内胚层细胞无法分化为大肝细胞,这表明内胚层细胞在体外分化需要脏壁中胚层的存在。添加肝细胞生长因子(HGF)、酸性成纤维细胞生长因子(aFGF)或碱性成纤维细胞生长因子(bFGF)在没有间充质的培养中也不支持肝内胚层细胞的存活或肝细胞分化。Matrigel和那些生长因子可能不是间充质的合适替代品。