Roles for Ndel1 in keratin organization and desmosome function

Mol Biol Cell. 2021 Oct 1;32(20):ar2. doi: 10.1091/mbc.E21-02-0087. Epub 2021 Jul 28.

Abstract

Keratin intermediate filaments form dynamic polymer networks that organize in specific ways dependent on the cell type, the stage of the cell cycle, and the state of the cell. In differentiated cells of the epidermis, they are organized by desmosomes, cell-cell adhesion complexes that provide essential mechanical integrity to this tissue. Despite this, we know little about how keratin organization is controlled and whether desmosomes locally regulate keratin dynamics in addition to binding preassembled filaments. Ndel1 is a desmosome-associated protein in the differentiated epidermis, though its function at these structures has not been examined. Here, we show that Ndel1 binds directly to keratin subunits through a motif conserved in all intermediate filament proteins. Further, Ndel1 was necessary for robust desmosome-keratin association and sufficient to reorganize keratins at distinct cellular sites. Lis1, a Ndel1 binding protein, was required for desmosomal localization of Ndel1, but not for its effects on keratin filaments. Finally, we use mouse genetics to demonstrate that loss of Ndel1 results in desmosome defects in the epidermis. Our data thus identify Ndel1 as a desmosome-associated protein that promotes local assembly/reorganization of keratin filaments and is essential for robust desmosome formation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Alkyl-2-acetylglycerophosphocholine Esterase / metabolism
  • Animals
  • Carrier Proteins / metabolism*
  • Cell Adhesion / physiology
  • Cell Differentiation
  • Cells, Cultured
  • Cytoskeleton / metabolism
  • Desmoplakins / metabolism
  • Desmosomes / metabolism*
  • Epidermal Cells / metabolism
  • Epidermis / metabolism
  • Intermediate Filaments / metabolism
  • Keratinocytes / metabolism
  • Keratins / metabolism*
  • Mice
  • Microtubule-Associated Proteins / metabolism

Substances

  • Carrier Proteins
  • Desmoplakins
  • Microtubule-Associated Proteins
  • Ndel1 protein, mouse
  • Keratins
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase
  • Pafah1b1 protein, mouse