IRSp53 controls plasma membrane shape and polarized transport at the nascent lumen in epithelial tubules

Nat Commun. 2020 Jul 14;11(1):3516. doi: 10.1038/s41467-020-17091-x.

Abstract

It is unclear whether the establishment of apical-basal cell polarity during the generation of epithelial lumens requires molecules acting at the plasma membrane/actin interface. Here, we show that the I-BAR-containing IRSp53 protein controls lumen formation and the positioning of the polarity determinants aPKC and podocalyxin. Molecularly, IRSp53 acts by regulating the localization and activity of the small GTPase RAB35, and by interacting with the actin capping protein EPS8. Using correlative light and electron microscopy, we further show that IRSp53 ensures the shape and continuity of the opposing plasma membrane of two daughter cells, leading to the formation of a single apical lumen. Genetic removal of IRSp53 results in abnormal renal tubulogenesis, with altered tubular polarity and architectural organization. Thus, IRSp53 acts as a membrane curvature-sensing platform for the assembly of multi-protein complexes that control the trafficking of apical determinants and the integrity of the luminal plasma membrane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Cell Membrane / metabolism*
  • Cell Polarity / genetics
  • Cell Polarity / physiology
  • Epithelial Cells / metabolism
  • Female
  • Humans
  • Morphogenesis / genetics
  • Morphogenesis / physiology
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Protein Transport / genetics
  • Protein Transport / physiology
  • Sialoglycoproteins / genetics
  • Sialoglycoproteins / metabolism
  • rab GTP-Binding Proteins / genetics
  • rab GTP-Binding Proteins / metabolism*

Substances

  • Actins
  • BAIAP2 protein, human
  • Nerve Tissue Proteins
  • Sialoglycoproteins
  • podocalyxin
  • RAB35 protein, human
  • rab GTP-Binding Proteins