Abstract

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.

Highlights

  • Epithelial branching morphogenesis has been observed to occur in vitro, in reconstituted basement membranes, as well as in vivo during early development (Grobstein, 1967; Taub et al, 1990; Unsworth and Grobstein, 1970)

  • We find that primary rabbit kidney cells do possess the capacity to form proximal tubules in matrigel, which accumulate Lucifer Yellow into the lumen of the tubules

  • Transepithelial solute transport occurs in renal proximal tubules with either complete or even with partially formed lumens To determine whether these ‘tubules’ were functional, the matrigel cultures were incubated with Lucifer Yellow, a fluorescent substrate of the p-aminohippurate (PAH) transport system (Masereeuw et al, 1999)

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Summary

Introduction

Epithelial branching morphogenesis has been observed to occur in vitro, in reconstituted basement membranes, as well as in vivo during early development (Grobstein, 1967; Taub et al, 1990; Unsworth and Grobstein, 1970). Ultrastructure studies indicate that matrigel is composed of a network of matrix proteins similar to the lamina densa in authentic basement membranes. The same proteins present in authentic basement membranes, which include laminin, collagen IV, heparan sulfate proteoglycan and nidogen/entactin, are present in matrigel (Kleinman et al, 1982). The presence of laminin in particular, as well as collagen IV in matrigel, provides this preparation the ability to promote tube formation by human umbilical cord endothelial cells in vitro (Grant et al, 1989)

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