ECM stiffness regulates glial migration in Drosophila and mammalian glioma models

Kim S., Jeibmann A., Halama K., Witte H., Wälte M., Matzat T., Schillers H., Faber C., Senner V., Paulus W., Klämbt C.

Research article (journal) | Peer reviewed

Abstract

Cell migration is an important feature of glial cells. Here, we used the Drosophila eye disc to decipher the molecular network controlling glial migration. We stimulated glial motility by pan-glial PDGF receptor (PVR) activation and identified several genes acting downstream of PVR. Drosophila lox is a non-essential gene encoding a secreted protein that stiffens the extracellular matrix (ECM). Glial-specific knockdown of Integrin results in ECM softening. Moreover, we show that lox expression is regulated by Integrin signaling and vice versa, suggesting that a positive-feedback loop ensures a rigid ECM in the vicinity of migrating cells. The general implication of this model was tested in a mammalian glioma model, where a Lox-specific inhibitor unraveled a clear impact of ECM rigidity in glioma cell migration. © 2014. Published by The Company of Biologists Ltd.

Details about the publication

JournalDevelopment
Volume141
Issue16
Page range3233-3242
StatusPublished
Release year2014
Language in which the publication is writtenEnglish
DOI10.1242/dev.106039
Link to the full texthttp://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84905498660&origin=inward
KeywordsDrosophila; Extracellular matrix; Glial cell migration; Human; Lox; Lysyl oxidase; Mouse; PDGF-receptor; PVR

Authors from the University of Münster

Klämbt, Christian
Professorship of Neuro- and Behavioral Biology (Prof. Klämbt)
Schillers, Hermann
Institute of Physiology II