Lack of Paxillin phosphorylation promotes single-cell migration in vivo

J Cell Biol. 2023 Mar 6;222(3):e202206078. doi: 10.1083/jcb.202206078. Epub 2023 Feb 1.

Abstract

Focal adhesions are structures that physically link the cell to the extracellular matrix for cell migration. Although cell culture studies have provided a wealth of information regarding focal adhesion biology, it is critical to understand how focal adhesions are dynamically regulated in their native environment. We developed a zebrafish system to visualize focal adhesion structures during single-cell migration in vivo. We find that a key site of phosphoregulation (Y118) on Paxillin exhibits reduced phosphorylation in migrating cells in vivo compared to in vitro. Furthermore, expression of a non-phosphorylatable version of Y118-Paxillin increases focal adhesion disassembly and promotes cell migration in vivo, despite inhibiting cell migration in vitro. Using a mouse model, we further find that the upstream kinase, focal adhesion kinase, is downregulated in cells in vivo, and cells expressing non-phosphorylatable Y118-Paxillin exhibit increased activation of the CRKII-DOCK180/RacGEF pathway. Our findings provide significant new insight into the intrinsic regulation of focal adhesions in cells migrating in their native environment.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cell Movement* / physiology
  • Focal Adhesion Protein-Tyrosine Kinases / metabolism
  • Focal Adhesions* / metabolism
  • Mice
  • Paxillin* / genetics
  • Paxillin* / metabolism
  • Phosphorylation
  • Zebrafish* / genetics
  • Zebrafish* / metabolism

Substances

  • Focal Adhesion Protein-Tyrosine Kinases
  • Paxillin