New insights into redox regulation of stem cell self-renewal and differentiation

Biochim Biophys Acta. 2015 Aug;1850(8):1518-26. doi: 10.1016/j.bbagen.2015.02.017. Epub 2015 Mar 10.

Abstract

Background: Reactive oxygen species (ROS), the natural byproducts of aerobic metabolism, are precisely orchestrated to evoke diverse signaling pathways. To date, studies have focused mainly on the detrimental effects of ROS in stem cells. Recently, accumulating evidence has suggested that ROS also function as second messengers that modulate stem cell self-renewal and differentiation by regulating intricate signaling networks. Although many efforts have been made to clarify the general effects of ROS on signal transduction in stem cells, less is known about the initial and direct executors of ROS signaling, which are known as 'redox sensors'.

Scope of review: Modifications of cysteine residues in redox sensors are of significant importance in the modulation of protein function in response to different redox conditions. Intriguingly, most key molecules in ROS signaling and cell cycle regulation (including transcriptional factors and kinases) that are crucial in the regulation of stem cell self-renewal and differentiation have the potential to be redox sensors.

Major conclusions: We highlight herein the importance of redox regulation of these key regulators in stem cell self-renewal and differentiation.

General significance: Understanding the mechanisms of redox regulation in stem cell self-renewal and differentiation will open exciting new perspectives for stem cell biology. This article is part of a Special Issue entitled Redox regulation of differentiation and de-differentiation.

Keywords: Cysteine; ROS; Redox modification; Self-renewal; Stem cell.

Publication types

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

MeSH terms

  • Cell Differentiation / genetics
  • Cell Differentiation / physiology*
  • Cell Proliferation*
  • MicroRNAs / genetics
  • Models, Biological
  • Oxidation-Reduction
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / genetics
  • Signal Transduction / physiology*
  • Stem Cells / cytology*
  • Stem Cells / metabolism
  • Sulfhydryl Compounds / metabolism
  • Transcription Factors / metabolism

Substances

  • MicroRNAs
  • Reactive Oxygen Species
  • Sulfhydryl Compounds
  • Transcription Factors