Sakurai H, Barros E J, Tsukamoto T, Barasch J, Nigam S K
Renal Division, Department of Medicine, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 1997 Jun 10;94(12):6279-84. doi: 10.1073/pnas.94.12.6279.
Interactions between the ureteric bud (UB) and metanephric mesenchyme are crucial for tubulogenesis during kidney development. Two immortalized cell lines derived from the day 11.5 embryonic kidney, UB cells, which appear to be epithelial (cytokeratin-positive, E-cadherin-positive, and ZO-1-positive by immunostaining) and BSN cells, which are largely mesenchymal (vimentin-positive, but negative for cytokeratin, cell surface E-cadherin, and cell surface ZO-1), were used to establish an in vitro tubulogenesis system. BSN cells expressed hepatocyte growth factor (HGF) and transforming growth factor-beta1 mRNAs, and its conditioned medium (BSN-CM) contained factors capable of activating the epidermal growth factor (EGF) receptor (EGFR). When UB cells were cultured in an extracellular matrix gel in the presence of the embryonic kidney or BSN-CM, the UB cells underwent morphogenetic changes characteristic of early in vitro branching tubulogenesis. These changes were largely inhibited by a combination of neutralizing anti-HGF antibodies and the EGFR inhibitor tyrphostin AG1478, suggesting that EGFR ligands, together with HGF, account for much of this early morphogenetic activity. Nevertheless, there was a significant fraction of tubulogenic activity that could not be inhibited, suggesting the existence of other soluble factors. Whereas HGF, EGF, transforming growth factor alpha, basic fibroblast growth factor (bFGF), and insulin-like growth factor 1 (IGF-1), or a mixture of these growth factors, induced epithelial processes for up to 3 days, only IGF-1, possibly bFGF, and the mixture were able to sustain morphogenesis for longer periods, though not nearly to the same degree as BSN-CM. Moreover, only BSN-CM induced branching tubular structures with clear lumens, consistent with the existence of other soluble factors crucial for the formation and/or maintenance of branching tubular structures with lumens in vitro.
在肾脏发育过程中,输尿管芽(UB)与后肾间充质之间的相互作用对于肾小管形成至关重要。从第11.5天胚胎肾脏衍生出两种永生化细胞系,即UB细胞(免疫染色显示其似乎为上皮细胞,细胞角蛋白阳性、E-钙黏蛋白阳性且ZO-1阳性)和BSN细胞(主要为间充质细胞,波形蛋白阳性,但细胞角蛋白、细胞表面E-钙黏蛋白和细胞表面ZO-1阴性),用于建立体外肾小管形成系统。BSN细胞表达肝细胞生长因子(HGF)和转化生长因子-β1 mRNA,其条件培养基(BSN-CM)含有能够激活表皮生长因子(EGF)受体(EGFR)的因子。当UB细胞在细胞外基质凝胶中于胚胎肾脏或BSN-CM存在的情况下培养时,UB细胞会发生早期体外分支肾小管形成特有的形态发生变化。这些变化在很大程度上被中和抗HGF抗体与EGFR抑制剂 tyrphostin AG1478的组合所抑制,这表明EGFR配体与HGF共同构成了这种早期形态发生活性的大部分原因。然而,仍有相当一部分肾小管形成活性无法被抑制,这表明存在其他可溶性因子。虽然HGF、EGF、转化生长因子α、碱性成纤维细胞生长因子(bFGF)和胰岛素样生长因子1(IGF-1),或这些生长因子的混合物,可诱导上皮突起长达3天,但只有IGF-1、可能还有bFGF以及该混合物能够在更长时间内维持形态发生过程,尽管程度远不及BSN-CM。此外,只有BSN-CM能诱导出具有清晰管腔的分支管状结构,这与存在其他对体外具有管腔的分支管状结构的形成和/或维持至关重要的可溶性因子一致。