Cell-Cycle Cross Talk with Caspases and Their Substrates

  1. Andreas Villunger1,2,3,4
  1. 1Division of Developmental Immunology, Biocenter, Medical University of Innsbruck, Innsbruck 6020, Austria
  2. 2Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna 1090, Austria
  3. 3CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna 1090, Austria
  1. Correspondence: andreas.villunger{at}i-med.ac.at
  1. 4 All authors contributed equally to this work.

Abstract

Caspases play central roles in mediating both cell death and inflammation. It has more recently become evident that caspases also drive other biological processes. Most prominently, caspases have been shown to be involved in differentiation. Several stem and progenitor cell types rely on caspases to initiate and execute their differentiation processes. These range from neural and glial cells, to skeletal myoblasts and osteoblasts, and several cell types of the hematopoietic system. Beyond differentiation, caspases have also been shown to play roles in other “noncanonical” processes, including cell proliferation, arrest, and senescence, thereby contributing to the mechanisms that regulate tissue homeostasis at multiple levels. Remarkably, caspases directly influence the course of the cell cycle in both a positive and negative manner. Caspases both cleave elements of the cell-cycle machinery and are themselves substrates of cell-cycle kinases. Here we aim to summarize the breadth of interactions between caspases and cell-cycle regulators. We also highlight recent developments in this area.



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      1. Cold Spring Harb. Perspect. Biol. 12: a036475 Copyright © 2020 Cold Spring Harbor Laboratory Press; all rights reserved

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