Zimrin A B, Villeponteau B, Maciag T
Department of Molecular Biology, Holland Laboratory, American Red Cross, Rockville, MD 20855, USA.
Biochem Biophys Res Commun. 1995 Aug 15;213(2):630-8. doi: 10.1006/bbrc.1995.2178.
Endothelial cells can be induced to form a branching network of tubular structures using a variety of cell culture conditions. We have examined this differentiation process using several sets of conditions: plating human umbilical vein endothelial cells (HUVEC) on Matrigel, adding collagen to the apical surface of HUVEC grown on fibronectin, and plating HUVEC on fibrin in the presence of FGF-1. We determined that although the first two conditions produce dramatic morphologic changes in the HUVEC population, gene transcription and translation are not required for the regulation of the process. Rather, post-translational events are involved since the Matrigel-dependent process could be inhibited by the addition of nocodazole, suramin or H7, a protein kinase inhibitor. In contrast, the fibrin matrix-dependent differentiation pathway involved transcriptional and translational events since the addition of either actinomycin D or cycloheximide inhibited this pathway. A modified differential display of RNA extracted from HUVEC after 0, 2, 5, and 24 hours on fibrin revealed expression of a novel cDNA.
利用多种细胞培养条件可诱导内皮细胞形成分支状管状结构网络。我们使用了几组条件来研究这种分化过程:将人脐静脉内皮细胞(HUVEC)接种于基质胶上,向生长在纤连蛋白上的HUVEC顶表面添加胶原蛋白,以及在存在FGF-1的情况下将HUVEC接种于纤维蛋白上。我们确定,尽管前两个条件在HUVEC群体中产生了显著的形态学变化,但该过程的调节并不需要基因转录和翻译。相反,由于基质胶依赖性过程可被诺考达唑、苏拉明或蛋白激酶抑制剂H7的添加所抑制,因此涉及翻译后事件。相比之下,纤维蛋白基质依赖性分化途径涉及转录和翻译事件,因为放线菌素D或环己酰亚胺的添加均抑制了该途径。对在纤维蛋白上培养0、2、5和24小时后的HUVEC提取的RNA进行改良差异显示,揭示了一种新cDNA的表达。