The differential activation of intracellular signaling pathways confers the permissiveness of embryonic stem cell derivation from different mouse strains

Development. 2015 Feb 1;142(3):431-7. doi: 10.1242/dev.112375. Epub 2015 Jan 6.

Abstract

The requirement of leukemia inhibitory factor (LIF) for the establishment and maintenance of mouse embryonic stem cells (ESCs) depends on the genetic background of the ESC origin. To reveal the molecular basis of the strain-dependent function of LIF, we compared the activation of the intracellular signaling pathways downstream of LIF in ESCs with different genetic backgrounds. We found that the JAK-Stat3 pathway was dominantly activated in ESCs derived from 'permissive' mouse strains (129Sv and C57BL6), whereas the MAP kinase pathway was hyperactivated in ESCs from 'non-permissive' strains (NOD, CBA and FVB). Artificial activation of Stat3 supported stable self-renewal of ESCs from non-permissive strains. These data suggest that the difference in the balance between the two intracellular signaling pathways underlies the differential response to LIF.

Keywords: Embryonic stem cell; LIF signaling; MAP kinase; Signal responsiveness; Stat3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA Primers / genetics
  • Embryonic Stem Cells / physiology*
  • Gene Expression Regulation, Developmental / genetics
  • Gene Expression Regulation, Developmental / physiology*
  • Janus Kinase 1 / metabolism
  • Leukemia Inhibitory Factor / metabolism*
  • Mice
  • Mice, Mutant Strains
  • Real-Time Polymerase Chain Reaction
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction / physiology*
  • Species Specificity

Substances

  • DNA Primers
  • Leukemia Inhibitory Factor
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • Jak1 protein, mouse
  • Janus Kinase 1