ß-arrestin control of late endosomal sorting facilitates decoy receptor function and chemokine gradient formation.

Mahabaleshwar H, Tarbashevich K, Nowak M, Brand M, Raz E

Research article (journal) | Peer reviewed

Abstract

A crucial regulator of Cxcl12 is the decoy receptor Cxcr7, which controls the level of the chemokine in the tissue. The molecular mechanisms that enable Cxcr7 to function as an efficient molecular sink are not known. Using zebrafish primordial germ cells as a model, we identify a novel role for ?-arrestins in controlling the intracellular trafficking of Cxcr7. ?-arrestins facilitate the recycling of Cxcr7 from late endosomal compartments back to the plasma membrane, whereas the internalized ligand undergoes lysosomal degradation. ?-arrestins thus function in regulating chemokine gradient formation, allowing responding cells to discriminate between alternative migration targets in vivo.

Details about the publication

JournalDevelopment
Volume139
Issue16
Page range2897-902
StatusPublished
Release year2012
Language in which the publication is writtenEnglish
DOI10.1242/dev.080408

Authors from the University of Münster

Raz, Erez
Institute of Cell Biology
Tarbashevich, Katsiaryna
Centre for Molecular Biology of Inflammation