Epigenetic Regulation of Transition Among Different Pluripotent States: Concise Review

Stem Cells. 2019 Nov;37(11):1372-1380. doi: 10.1002/stem.3064. Epub 2019 Aug 14.

Abstract

The extraordinary progress of pluripotent stem cell research provides a revolutionary avenue to understand mammalian early embryonic development. Besides well-established conventional mouse and human embryonic stem cells, the discoveries of naive state human stem cell, two-cell-like cell, and the newly defined "extended pluripotent" stem cell and "expanded potential" stem cell with bidirectional chimeric ability have greatly broadened the horizons of more pluripotent states recaptured and maintained in dish, infinitely approaching the totipotent blastomere state. Although all these pluripotent cell types can self-renew and have the ability to differentiate into all the three germ layers, accumulating evidence suggests that these pluripotent states display distinct epigenetic characters. More strikingly, epigenetic reprogramming, including DNA methylation, histone modification, and chromatin remodeling, is required to reset the cell fate commitment, suggesting that epigenetic mechanisms may play an active and important role in the maintenance and transition among these pluripotent states. Here, we have reviewed studies on various pluripotent states, with a highlight on the epigenetic regulation during the interconversion. Stem Cells 2019;37:1372-1380.

Keywords: Epigenetics; Expanded potential stem cell; Extended pluripotent stem cell; Naive pluripotency; Pluripotency; Totipotency; Two-cell-like.

Publication types

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

MeSH terms

  • Animals
  • Cellular Reprogramming / genetics
  • Cellular Reprogramming / physiology
  • Chromatin Assembly and Disassembly / genetics
  • Chromatin Assembly and Disassembly / physiology
  • DNA Methylation / genetics
  • DNA Methylation / physiology
  • Epigenesis, Genetic / genetics*
  • Gene Expression Regulation, Developmental / physiology
  • Histones / metabolism
  • Humans
  • Pluripotent Stem Cells / cytology*
  • Pluripotent Stem Cells / metabolism*

Substances

  • Histones