학술논문

A crucial role for b2 integrins in podosome formation, dynamics and Toll-like-receptor-signaled disassembly in dendritic cells.
Document Type
Article
Source
Journal of Cell Science. Oct2014, Vol. 127 Issue 19, p4213-4224. 12p. 7 Graphs.
Subject
*INTEGRINS
*CELLULAR signal transduction
*PHOSPHORYLATION
*FORMATION of focal adhesions
*DENDRITIC cells
*TOLL-like receptors
*CELL migration
Language
ISSN
0021-9533
Abstract
The dynamic properties of podosomes, their ability to degrade the underlying matrix and their modulation by Toll-like receptor (TLR) signaling in dendritic cells (DCs) suggests they have an important role in migration. Integrins are thought to participate in formation and dynamics of podosomes but the multiplicity of integrins in podosomes has made this difficult to assess. We report that murine DCs that lack ß2 integrins fail to form podosomes. Re-expression of ß2 integrins restored podosomes but not when the membrane proximal or distal NPxF motifs, or when an intervening triplet of threonine residues were mutated. We show that ß2 integrins are remarkably long-lived in podosome clusters and form a persistent framework that hosts multiple actin-core-formation events at the same or adjacent sites. When ß2 integrin amino acid residues 745 or 756 were mutated from Ser to Ala, podosomes became resistant to dissolution mediated through TLR signaling. TLR signaling did not detectably modulate phosphorylation at these sites but mutation of either residue to phospho-mimetic Asp increased ß2 integrin turnover in podosomes, indicating that phosphorylation at one or both sites establishes permissive conditions for TLR-signaled podosome disassembly. [ABSTRACT FROM AUTHOR]