Han Ho Jae, Sigurdson Wade J, Nickerson Peter A, Taub Mary
Department of Veterinary Physiology, College of Veterinary Medicine, Hormone Research Center, Chonnam National University, Gwangju 500-757, Korea.
J Cell Sci. 2004 Apr 1;117(Pt 9):1821-33. doi: 10.1242/jcs.01020. Epub 2004 Mar 16.
Tubules may arise during branching morphogenesis through several mechanisms including wrapping, budding, cavitation and cord hollowing. In this report we present evidence that is consistent with renal proximal tubule formation through a process of cord hollowing (a process that requires the concomitant establishment of apicobasal polarity and lumen formation). Pockets of lumen filled with Lucifer Yellow were observed within developing cords of rabbit renal proximal tubule cells in matrigel. The observation of Lucifer Yellow accumulation suggests functional polarization. In the renal proximal tubule Lucifer Yellow is initially transported intracellularly by means of a basolaterally oriented p-aminohippurate transport system, followed by apical secretion into the lumen of the nephron. Consistent with such polarization in developing tubules, Triticum vulgare was observed to bind to the lumenal membranes within pockets of Lucifer Yellow-filled lumens. As this lectin binds apically in the rabbit renal proximal tubule, T. vulgare binding is indicative of the emergence of an apical domain before the formation of a contiguous lumen. Both epidermal growth factor and hepatocyte growth factor stimulated the formation of transporting tubules. The stimulatory effect of both epidermal growth factor and hepatocyte growth factor on tubulogenesis was inhibited by PD98059, a mitogen activated protein kinase kinase inhibitor, rather than by wortmannin, an inhibitor of phosphoinositide 3-kinase. Nevertheless, Lucifer Yellow-filled lumens were observed in tubules that formed in the presence of PD98059 as well as with wortmannin, indicating that these drugs did not prevent the process of cavitation. By contrast, rapamycin, an inhibitor of the mammalian target of rapamycin, prevented the process of cavitation without affecting the frequency of formation of developing cords. Multicellular cysts were observed to form in 8-bromocyclic AMP-treated cultures. As these cysts did not similarly accumulate Lucifer Yellow lumenally, it is very likely that processes other than organic anion accumulation are involved in the process of cystogenesis, including the Na,K-ATPase.
肾小管可能在分支形态发生过程中通过多种机制形成,包括包裹、出芽、空泡化和索状中空。在本报告中,我们提供的证据表明,肾近端小管是通过索状中空过程形成的(该过程需要同时建立顶-基极性和管腔形成)。在基质胶中培养的兔肾近端小管细胞发育索内观察到充满路西法黄的管腔囊。路西法黄积累的观察结果表明存在功能极化。在肾近端小管中,路西法黄最初通过基底外侧定向的对氨基马尿酸转运系统在细胞内运输,随后通过顶端分泌进入肾单位管腔。与发育中小管的这种极化一致,观察到普通小麦凝集素与充满路西法黄的管腔囊内的管腔膜结合。由于这种凝集素在兔肾近端小管中与顶端结合,普通小麦凝集素的结合表明在连续管腔形成之前顶端结构域已经出现。表皮生长因子和肝细胞生长因子均刺激了转运小管的形成。有丝分裂原活化蛋白激酶激酶抑制剂PD98059抑制了表皮生长因子和肝细胞生长因子对小管形成的刺激作用,而磷酸肌醇3激酶抑制剂渥曼青霉素则没有这种作用。然而,在存在PD98059以及渥曼青霉素的情况下形成的小管中也观察到了充满路西法黄的管腔,这表明这些药物并没有阻止空泡化过程。相比之下,雷帕霉素(一种雷帕霉素哺乳动物靶点抑制剂)阻止了空泡化过程,而不影响发育索形成的频率。在经8-溴环磷酸腺苷处理的培养物中观察到形成了多细胞囊肿。由于这些囊肿在管腔内没有类似地积累路西法黄,很可能在囊肿形成过程中涉及除有机阴离子积累之外的其他过程,包括钠钾ATP酶。