Leukocyte Cytoskeleton Polarization Is Initiated by Plasma Membrane Curvature from Cell Attachment

Chunguang Ren, Qianying Yuan, Martha Braun, Xia Zhang, Björn Petri, Jiasheng Zhang, Dongjoo Kim, Julia Guez-Haddad, Wenzhi Xue, Weijun Pan, Rong Fan, Paul Kubes, Zhaoxia Sun, Yarden Opatowsky, Franck Polleux, Erdem Karatekin, Wenwen Tang, Dianqing Wu

Research output: Contribution to journalArticlepeer-review

Abstract

Cell polarization is important for various biological processes. However, its regulation, particularly initiation, is incompletely understood. Here, we investigated mechanisms by which neutrophils break their symmetry and initiate their cytoskeleton polarization from an apolar state in circulation for their extravasation during inflammation. We show here that a local increase in plasma membrane (PM) curvature resulting from cell contact to a surface triggers the initial breakage of the symmetry of an apolar neutrophil and is required for subsequent polarization events induced by chemical stimulation. This local increase in PM curvature recruits SRGAP2 via its F-BAR domain, which in turn activates PI4KA and results in PM PtdIns4P polarization. Polarized PM PtdIns4P is targeted by RPH3A, which directs PIP5K1C90 and subsequent phosphorylated myosin light chain polarization, and this polarization signaling axis regulates neutrophil firm attachment to endothelium. Thus, this study reveals a mechanism for the initiation of cell cytoskeleton polarization. The molecular mechanisms controlling cell polarization are incompletely understood. Ren and Yuan et al. show that local increase in plasma membrane (PM) curvature resulting from cell attachment recruits and polarizes an inverse FBAR domain protein SRGAP2 to initiate cell cytoskeleton polarization, which is important for neutrophil adhesion to endothelium.

Original languageEnglish
Pages (from-to)206-219.e7
JournalDevelopmental Cell
Volume49
Issue number2
DOIs
StatePublished - 22 Apr 2019

Keywords

  • BAR domain
  • SRGAP2
  • adhesion
  • cell polarization
  • neutrophil
  • phosphatidylinositol-4-phosphate

All Science Journal Classification (ASJC) codes

  • General Biochemistry,Genetics and Molecular Biology
  • Molecular Biology
  • Cell Biology
  • Developmental Biology

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