Substrate engagement of integrins α5β1 and αvβ3 is necessary, but not sufficient, for high directional persistence in migration on fibronectin

The interplay between specific integrin-mediated matrix adhesion and directional persistence in cell migration is not well understood. Here, we characterized fibroblast adhesion and migration on the extracellular matrix glycoproteins fibronectin and vitronectin, focusing on the role of α5β1 and αvβ3...

Full description

Saved in:
Bibliographic Details
Main Authors: Missirlis, Dimitris (Author) , Haraszti, Tamás (Author) , Scheele, Catharina (Author) , Wiegand, Tina (Author) , Diaz, Carolina (Author) , Neubauer, Stefanie (Author) , Rechenmacher, Florian (Author) , Kessler, Horst (Author) , Spatz, Joachim P. (Author)
Format: Article (Journal)
Language:English
Published: 18 March 2016
In: Scientific reports
Year: 2016, Volume: 6
ISSN:2045-2322
DOI:10.1038/srep23258
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1038/srep23258
Verlag, lizenzpflichtig, Volltext: https://www.nature.com/articles/srep23258
Get full text
Author Notes:Dimitris Missirlis, Tamás Haraszti, Catharina v C. Scheele, Tina Wiegand, Carolina Diaz, Stefanie Neubauer, Florian Rechenmacher, Horst Kessler & Joachim P. Spatz
Description
Summary:The interplay between specific integrin-mediated matrix adhesion and directional persistence in cell migration is not well understood. Here, we characterized fibroblast adhesion and migration on the extracellular matrix glycoproteins fibronectin and vitronectin, focusing on the role of α5β1 and αvβ3 integrins. Fibroblasts manifested high directional persistence in migration on fibronectin-, but not vitronectin-coated substrates, in a ligand density-dependent manner. Fibronectin stimulated α5β1-dependent organization of the actin cytoskeleton into oriented, ventral stress fibers and assembly of dynamic, polarized protrusions, characterized as regions free of stress fibers and rich in nascent adhesions at their edge. Such protrusions correlated with persistent, local leading edge advancement, but were not sufficient, nor necessary for directional migration over longer times. Selective blocking of αvβ3 or α5β1 integrins using small molecule integrin antagonists reduced directional persistence on fibronectin, indicating integrin cooperativity in maintaining directionality. On the other hand, patterned substrates, designed to selectively engage either integrin, or their combination, were not sufficient to establish directional migration. Overall, our study demonstrates adhesive coating-dependent regulation of directional persistence in fibroblast migration and challenges the generality of the previously suggested role of β1 and β3 integrins in directional migration.
Item Description:Im Titel sind die Zahlen "5", "1", "3" sowie das Zeichen "v" tiefgestellt
Gesehen am 23.06.2020
Physical Description:Online Resource
ISSN:2045-2322
DOI:10.1038/srep23258