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First published online 7 July 2009
doi: 10.1242/jcs.039347
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Research Article |
The Cell Microscopy Centre, Department of Cell Biology and Institute of Biomembrane, University Medical Centre Utrecht, AZU Rm G02.525, Heidelberglaan 100, 3584CX Utrecht, The Netherlands
* Author for correspondence (e-mail: c.rabouille{at}umcutrecht.nl)
Accepted 22 April 2009
During the epithelium remodelling such as the flattening of the Drosophila follicular epithelium, the
-integrin subunits are unconventionally secreted through a dGRASP-dependent route that is built de novo. The biogenetic process starts with the upregulation of a small subset of targeted mRNAs, including dgrasp. Here, we show that dgrasp mRNA upregulation is triggered by the tension of the underlying oocyte and by applied external forces at the basal side of the follicular epithelium. We show that integrins are also involved in dgrasp mRNA upregulation and the epithelium remodelling. Tension leads to the recruitment of RhoA to the plasma membrane, where it participates in its remodelling. The LIM protein PINCH can cycle to the nucleus and is involved in dgrasp mRNA upregulation. We propose that integrins are involved in triggering the biogenesis of their own unconventional secretion route that they use to strengthen adhesion and ensure epithelial integrity at the next stages of development, perhaps by acting as mechanosensors of the underlying tension through RhoA and PINCH.
Key words: Integrins, Epithelium, Drosophila, RhoA, PINCH, LIM, dgrasp, RNA upregulation, Targeting, Mechano-sensing
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