Tushir Jogender Singh, D'Souza-Schorey Crislyn
Department of Biological Sciences, University of Notre Dame, Notre Dame, IN 46656, USA.
EMBO J. 2007 Apr 4;26(7):1806-19. doi: 10.1038/sj.emboj.7601644. Epub 2007 Mar 15.
Tubules are the building blocks of epithelial organs and form in response to cues derived from morphogens such as hepatocyte growth factor (HGF). Relatively little is known about signaling pathways that orchestrate the cellular behaviors that constitute tubule development. Here, using three-dimensional cell cultures of Madin-Darby canine kidney cells, we show that the ARF6 GTPase is a critical determinant of tubule initiation in response to HGF. ARF6 is transiently activated during tubulogenesis and perturbing the ARF6 GTP/GDP cycle by inducible expression of ARF6 mutants defective in GTP binding or hydrolysis, inhibits the development of mature tubules. Further, we show that activation of ARF6 is necessary and sufficient to initiate tubule extension. The effect of ARF6 on tubule initiation is two-fold. First, ARF6 regulates the subcellular distribution of the GTPase, Rac1, to tubule extensions. Second, ARF6-induced ERK activation regulates Rac1 activation during tubule initiation through the expression of the receptor for urokinase type plasminogen activator. Thus, we have identified a cellular apparatus downstream of ARF6 activation, which regulates membrane and cytoskeleton remodeling necessary for the early stages of tubule development.
肾小管是上皮器官的基本组成部分,其形成是对诸如肝细胞生长因子(HGF)等形态发生素所衍生信号的响应。对于协调构成肾小管发育的细胞行为的信号通路,我们了解得相对较少。在此,利用麦迪逊-达比犬肾细胞的三维细胞培养,我们发现ARF6 GTP酶是响应HGF时肾小管起始的关键决定因素。ARF6在肾小管发生过程中短暂激活,通过诱导表达在GTP结合或水解方面存在缺陷的ARF6突变体来干扰ARF6 GTP/GDP循环,会抑制成熟肾小管的发育。此外,我们表明ARF6的激活对于启动肾小管延伸是必要且充分的。ARF6对肾小管起始的影响具有两方面。首先,ARF6将GTP酶Rac1的亚细胞分布调节至肾小管延伸部位。其次,ARF6诱导的ERK激活通过尿激酶型纤溶酶原激活剂受体的表达在肾小管起始过程中调节Rac1的激活。因此,我们确定了ARF6激活下游的一种细胞机制,其调节肾小管发育早期阶段所需的膜和细胞骨架重塑。