Bowes R C, Lightfoot R T, Van De Water B, Stevens J L
Campbell University School of Pharmacy, Department of Pharmaceutical Sciences, Buies Creek, North Carolina 27506, USA.
J Cell Physiol. 1999 Jul;180(1):81-90. doi: 10.1002/(SICI)1097-4652(199907)180:1<81::AID-JCP9>3.0.CO;2-J.
Hepatocyte growth factor (HGF)-induced tubulogenesis has been demonstrated with renal epithelial cell lines grown in collagen gels but not with primary cultured renal proximal tubular epithelial cells (RPTEs). We show that HGF selectively induces proliferation and branching morphogenesis of primary cultured rat RPTEs. Additional growth factors including fibroblast growth factor (FGF)-1, epidermal growth factor (EGF), FGF-7, or insulin-like growth factor-1 (IGF-1) did not selectively induce tubulogenesis. However, when administered in combination, these factors initiated branching morphogenesis comparable to HGF alone and greatly augmented HGF-induced proliferation and branching. Microscopic analysis revealed that branching RPTEs were undergoing tubulogenesis and formed a polarized epithelium. TGF-beta1 blocked HGF- or growth factor cocktail (GFC; HGF, FGF-1, EGF, IGF-1)-induced proliferation and branching morphogenesis. Adding TGF-beta1 after GFC-induced tubulogenesis had occurred caused a progressive regression of the tubular structures, a response associated with an increase in apoptosis of the RPTEs. Primary cultured RPTEs are capable of undergoing HGF-induced tubulogenesis. Unlike cell lines, combinations of growth factors differentially augment the response.
肝细胞生长因子(HGF)诱导的肾小管形成已在胶原凝胶中培养的肾上皮细胞系中得到证实,但原代培养的肾近端小管上皮细胞(RPTEs)却未出现这种情况。我们发现,HGF可选择性地诱导原代培养的大鼠RPTEs增殖和分支形态发生。包括成纤维细胞生长因子(FGF)-1、表皮生长因子(EGF)、FGF-7或胰岛素样生长因子-1(IGF-1)在内的其他生长因子均不能选择性地诱导肾小管形成。然而,当联合使用这些因子时,它们引发的分支形态发生与单独使用HGF时相当,并且极大地增强了HGF诱导的增殖和分支。显微镜分析显示,发生分支的RPTEs正在进行肾小管形成并形成了极化上皮。转化生长因子(TGF)-β1可阻断HGF或生长因子混合物(GFC;HGF、FGF-1、EGF、IGF-1)诱导的增殖和分支形态发生。在GFC诱导的肾小管形成发生后添加TGF-β1会导致管状结构逐渐退化,这种反应与RPTEs凋亡增加有关。原代培养的RPTEs能够发生HGF诱导的肾小管形成。与细胞系不同,生长因子的组合对反应的增强存在差异。