Prohibitin 2 regulates the proliferation and lineage-specific differentiation of mouse embryonic stem cells in mitochondria

PLoS One. 2014 Apr 7;9(4):e81552. doi: 10.1371/journal.pone.0081552. eCollection 2014.

Abstract

Background: The pluripotent state of embryonic stem (ES) cells is controlled by a network of specific transcription factors. Recent studies also suggested the significant contribution of mitochondria on the regulation of pluripotent stem cells. However, the molecules involved in these regulations are still unknown.

Methodology/principal findings: In this study, we found that prohibitin 2 (PHB2), a pleiotrophic factor mainly localized in mitochondria, is a crucial regulatory factor for the homeostasis and differentiation of ES cells. PHB2 was highly expressed in undifferentiated mouse ES cells, and the expression was decreased during the differentiation of ES cells. Knockdown of PHB2 induced significant apoptosis in pluripotent ES cells, whereas enhanced expression of PHB2 contributed to the proliferation of ES cells. However, enhanced expression of PHB2 strongly inhibited ES cell differentiation into neuronal and endodermal cells. Interestingly, only PHB2 with intact mitochondrial targeting signal showed these specific effects on ES cells. Moreover, overexpression of PHB2 enhanced the processing of a dynamin-like GTPase (OPA1) that regulates mitochondrial fusion and cristae remodeling, which could induce partial dysfunction of mitochondria.

Conclusions/significance: Our results suggest that PHB2 is a crucial mitochondrial regulator for homeostasis and lineage-specific differentiation of ES cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / physiology*
  • Cell Line
  • Cell Lineage / physiology*
  • Cell Proliferation / physiology*
  • Embryonic Stem Cells / cytology
  • Embryonic Stem Cells / metabolism*
  • Gene Expression Regulation / physiology
  • Mediator Complex / biosynthesis
  • Mediator Complex / genetics
  • Mice
  • Mitochondria / genetics
  • Mitochondria / metabolism
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism*
  • Prohibitins
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*

Substances

  • Med12 protein, mouse
  • Mediator Complex
  • Mitochondrial Proteins
  • Phb2 protein, mouse
  • Prohibitins
  • Repressor Proteins

Grants and funding

This work was supported by Grant-in-Aid for Scientific Research (17510165 and 20610008). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.