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.

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

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 zur Publikation

FachzeitschriftDevelopment
Jahrgang / Bandnr. / Volume141
Ausgabe / Heftnr. / Issue16
Seitenbereich3233-3242
StatusVeröffentlicht
Veröffentlichungsjahr2014
Sprache, in der die Publikation verfasst istEnglisch
DOI10.1242/dev.106039
Link zum Volltexthttp://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84905498660&origin=inward
StichwörterDrosophila; Extracellular matrix; Glial cell migration; Human; Lox; Lysyl oxidase; Mouse; PDGF-receptor; PVR

Autor*innen der Universität Münster

Klämbt, Christian
Professur für Neuro- und Verhaltensbiologie (Prof. Klämbt)
Schillers, Hermann
Institut für Physiologie II