A kindlin-3-leupaxin-paxillin signaling pathway regulates podosome stability

J Cell Biol. 2019 Oct 7;218(10):3436-3454. doi: 10.1083/jcb.201903109. Epub 2019 Sep 19.

Abstract

Binding of kindlins to integrins is required for integrin activation, stable ligand binding, and subsequent intracellular signaling. How hematopoietic kindlin-3 contributes to the assembly and stability of the adhesion complex is not known. Here we report that kindlin-3 recruits leupaxin into podosomes and thereby regulates paxillin phosphorylation and podosome turnover. We demonstrate that the activity of the protein tyrosine phosphatase PTP-PEST, which controls paxillin phosphorylation, requires leupaxin. In contrast, despite sharing the same binding mode with leupaxin, paxillin recruitment into podosomes is kindlin-3 independent. Instead, we found paxillin together with talin and vinculin in initial adhesion patches of kindlin-3-null cells. Surprisingly, despite its presence in these early adhesion patches, podosomes can form in the absence of paxillin or any paxillin member. In conclusion, our findings show that kindlin-3 not only activates and clusters integrins into podosomes but also regulates their lifetime by recruiting leupaxin, which controls PTP-PEST activity and thereby paxillin phosphorylation and downstream signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion
  • Cell Adhesion Molecules / metabolism*
  • Cells, Cultured
  • Chromatography, Liquid
  • Cytoskeletal Proteins / deficiency
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Paxillin / metabolism*
  • Podosomes / metabolism*
  • RAW 264.7 Cells
  • Signal Transduction*
  • Tandem Mass Spectrometry
  • Transcription Factors / metabolism*

Substances

  • Cell Adhesion Molecules
  • Cytoskeletal Proteins
  • Lpxn protein, mouse
  • Paxillin
  • Pxn protein, mouse
  • Transcription Factors
  • kindlin-3 protein, mouse