Macroautophagy supports Sonic Hedgehog signaling by promoting Patched1 degradation

Biochim Biophys Acta Mol Cell Res. 2021 Nov;1868(12):119124. doi: 10.1016/j.bbamcr.2021.119124. Epub 2021 Aug 20.

Abstract

Autophagy is a highly conservative self-digestion process to maintain intracellular homeostasis and to ensure the survival of cells under stress. Activation of Sonic Hedgehog (Shh) signaling depends on the normal endocytic degradation of pathway receptor Patched1 (Ptch1). It is unclear whether autophagy participates in the receptor endocytosis and modulates Shh signaling transduction. Here we found that blocking macroautophagy attenuates Shh signaling due to the failed transport of Smoothened (Smo) into primary cilia. At the upstream of Smo, Ptch1 was poly-ubiquitinated through K63-conjugated ubiquitin chains. Macroautophagy participates Shh-induced degradation of poly-ubiquitinated Ptch1, contributing to the activation of Shh signaling.

Keywords: Autophagy; Degradation; Patched1; Primary cilia; Shh signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy*
  • Cells, Cultured
  • Cilia / metabolism
  • HEK293 Cells
  • Hedgehog Proteins / metabolism*
  • Humans
  • Mice
  • Patched-1 Receptor / metabolism*
  • Proteolysis*
  • Signal Transduction
  • Smoothened Receptor / metabolism
  • Ubiquitination

Substances

  • Hedgehog Proteins
  • Patched-1 Receptor
  • Ptch1 protein, mouse
  • Shh protein, mouse
  • Smo protein, mouse
  • Smoothened Receptor