Matsubara Y, Ichinose M, Yahagi N, Tsukada S, Oka M, Miki K, Kimura S, Omata M, Shiokawa K, Kitamura N, Kaneko Y, Fukamachi H
Department of Internal Medicine, Faculty of Medicine, Department of Biological Sciences, Graduate School of Science, University of Tokyo, Japan.
Biochem Biophys Res Commun. 1998 Dec 18;253(2):477-84. doi: 10.1006/bbrc.1998.9808.
The role played by the hepatocyte growth factor activator (HGFA) during morphogenesis of the gastrointestinal tract was investigated in fetal rats between days 16 and 21 of gestation. By our recently established method using chelation and dissecting microscope, samples could be separated into epithelium and mesenchyme, essentially without cross-contamination. The expression of the gene for HGFA together with those for hepatocyte growth factor (HGF) and its receptor, c-met, was investigated in each tissue element by RT-PCR. In the fetal rat gastrointestinal tract, mRNA signals for the HGFA gene were observed only in epithelia expressing c-met mRNA. In contrast, expression of HGF mRNA was limited to the mesenchymal elements, indicating the presence of a local HGF system in the gastrointestinal tract; an inactive form of HGF (proHGF) is secreted from the mesenchyme and then cleaved into the active form by HGFA secreted by the target epithelia. During the period of morphogenesis and histodifferentiation in the gastrointestinal tract, enhanced expression of the genes for HGF and its receptor/c-met was evident, with elevated HGFA mRNA level observed throughout the gastrointestinal tract except in the forestomach, where mRNA expression was barely detectable. These results strongly suggest the possibility that morphogenesis of the gastrointestinal tract is regulated not only by a local increase in production of HGF, but also by enhanced proteolytic activation of proHGF. Thus, it is probable that locally synthesized HGFA plays a significant role as a regulator of the morphogenic action of HGF during gastrointestinal tract development.
在妊娠第16至21天的胎鼠中,研究了肝细胞生长因子激活剂(HGFA)在胃肠道形态发生过程中所起的作用。通过我们最近建立的使用螯合和解剖显微镜的方法,样本可基本无交叉污染地分离为上皮和间充质。通过逆转录聚合酶链反应(RT-PCR)研究了HGFA基因以及肝细胞生长因子(HGF)及其受体c-met基因在每个组织成分中的表达。在胎鼠胃肠道中,仅在表达c-met mRNA的上皮中观察到HGFA基因的mRNA信号。相反,HGF mRNA的表达仅限于间充质成分,这表明胃肠道中存在局部HGF系统;无活性形式的HGF(proHGF)从间充质分泌,然后被靶上皮分泌的HGFA切割成活性形式。在胃肠道形态发生和组织分化期间,HGF及其受体/c-met基因的表达明显增强,除前胃外,整个胃肠道中HGFA mRNA水平升高,在前胃中mRNA表达几乎检测不到。这些结果有力地表明,胃肠道形态发生不仅受HGF产生局部增加的调节,还受proHGF蛋白水解激活增强的调节。因此,局部合成的HGFA很可能在胃肠道发育过程中作为HGF形态发生作用的调节剂发挥重要作用。