Activation-Induced Cytidine Deaminase Regulates Fibroblast Growth Factor/Extracellular Signal-Regulated Kinases Signaling to Achieve the Naïve Pluripotent State During Reprogramming. Academic Article uri icon

Overview

abstract

  • Induced pluripotent stem cells (iPSCs) derived by in vitro reprogramming of somatic cells retain the capacity to self-renew and to differentiate into many cell types. Pluripotency encompasses multiple states, with naïve iPSCs considered as ground state, possessing high levels of self-renewal capacity and maximum potential without lineage restriction. We showed previously that activation-induced cytidine deaminase (AICDA) facilitates stabilization of pluripotency during reprogramming. Here, we report that Acida-/- iPSCs, even when successfully reprogrammed, fail to achieve the naïve pluripotent state and remain primed for differentiation because of a failure to suppress fibroblast growth factor (FGF)/extracellular signal-regulated kinases (ERK) signaling. Although the mutant cells display marked genomic hypermethylation, suppression of FGF/ERK signaling by AICDA is independent of deaminase activity. Thus, our study identifies AICDA as a novel regulator of naïve pluripotency through its activity on FGF/ERK signaling. Stem Cells 2019;37:1003-1017.

publication date

  • May 8, 2019

Research

keywords

  • Cellular Reprogramming
  • Cytidine Deaminase
  • Extracellular Signal-Regulated MAP Kinases
  • Fibroblast Growth Factors
  • Induced Pluripotent Stem Cells
  • MAP Kinase Signaling System

Identity

PubMed Central ID

  • PMC6766926

Scopus Document Identifier

  • 85065662498

Digital Object Identifier (DOI)

  • 10.1002/stem.3023

PubMed ID

  • 31021461

Additional Document Info

volume

  • 37

issue

  • 8