Impact of human CD95 mutations on cell death and autoimmunity: a model

Trends Immunol. 2022 Jan;43(1):22-40. doi: 10.1016/j.it.2021.11.006. Epub 2021 Dec 3.

Abstract

CD95/Fas/APO-1 can trigger apoptotic as well as nonapoptotic pathways in immune cells. CD95 signaling in humans can be inhibited by several mechanisms, including mutations in the gene encoding CD95. CD95 mutations lead to autoimmune disorders, such as autoimmune lymphoproliferative syndrome (ALPS). Gaining further insight into the reported mutations of CD95 and resulting alterations of its signaling networks may provide further understanding of their presumed role in certain autoimmune diseases. For illustrative purposes and to better understand the potential outcomes of CD95 mutations, here we assign their positions to the recently determined 3D structures of human CD95. Based on this, we make certain predictions and speculate on the putative role of CD95 mutation defects in CD95-mediated signaling for certain autoimmune diseases.

Keywords: 3D structure; ALPS; CD95; apoptosis; autoimmune disease; mutation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Apoptosis / genetics
  • Autoimmune Diseases* / genetics
  • Autoimmunity / genetics
  • Cell Death / genetics
  • Humans
  • Lymphoproliferative Disorders* / genetics
  • Mutation / genetics
  • fas Receptor / genetics*
  • fas Receptor / metabolism

Substances

  • FAS protein, human
  • fas Receptor