Abstract

The intercalation of mesenchymal cells into epithelia, through mesenchymal-to-epithelial transition (MET), underlies organogenesis, for example, in nephrogenesis, and tissue regeneration, during cell renewal and wound repair. Despite its importance, surprisingly little is known about the mechanisms that bring about MET in comparison with the related and much-studied, reverse process, epithelial-to-mesenchymal transition (EMT). We analyse the molecular events that regulate MET as stellate cells integrate into the established epithelium of the developing renal tubules in Drosophila. We show that stellate cells polarise as they integrate between epithelial principal cells and that the normal, localised expression of cell polarity proteins in principal cells is required for stellate cells to become epithelial. While the basolateral and apical membranes act as cues for stellate cell polarity, adherens junction integrity is required to regulate their movement through the epithelium; in the absence of these junctions stellate cells continue migrating into the tubule lumen. We also show that expression of basolateral proteins in stellate cells is a prerequisite for their ingression between principal cells. We present a model in which the contacts with successive principal cell membrane domains made by stellate cells as they integrate between them act as a cue for the elaboration of stellate cell polarity. We suggest that the formation of zonula adherens junctions between new cell neighbours establishes their apico-basal positions and stabilises them in the epithelium.

Highlights

  • During embryonic development diverse cell types migrate over large distances and merge with other cell populations to form complex organs

  • Studies of cells undergoing the reverse process, epithelial-to-mesenchymal transition (EMT), have revealed a tight correlation between a decrease in the levels of E-Cadherin (E-Cad) and adhesive junctions, and loss of apico-basal polarity, with a gain in cell motility (reviewed in Moreno-Bueno et al (2008). This suggests that polarity and adhesion may act to restrict cell motility and retain cells within an epithelium. We investigated this question in the renal tubules of Drosophila, where the ability of cells to undergo mesenchymal-to-epithelial transition (MET) is central to the development of this tissue

  • By mid-late stage 14 the process of stellate cell intercalation into the tubules is complete. While those found in the kink region, and just proximal to the kink remain clustered together, stellate cells found more distally in the tubules tend to be separated by principal cells (Fig. 1B)

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Summary

Introduction

During embryonic development diverse cell types migrate over large distances and merge with other cell populations to form complex organs. MECHANISMS OF DEVELOPMENT 127 (2010) 345–357 kidney develop via the recruitment of mesenchymal cells to the ureteric buds These cells undergo MET to form the renal tubules (Saxon, 1987). Studies of cells undergoing the reverse process, EMT, have revealed a tight correlation between a decrease in the levels of E-Cadherin (E-Cad) and adhesive junctions, and loss of apico-basal polarity, with a gain in cell motility (reviewed in Moreno-Bueno et al (2008). This suggests that polarity and adhesion may act to restrict cell motility and retain cells within an epithelium. In an interesting comparison with the process of EMT, polarity and adhesion are shown to be key regulators of MET

Results and discussion
Drosophila stocks and genetics
Immunohistochemistry
Image acquisition and manipulation
Full Text
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