Secreted Ephrin Receptor A7 Promotes Somatic Cell Reprogramming by Inducing ERK Activity Reduction

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Joonseong Lee - , Kyoto University (Author)
  • May Nakajima-Koyama - , Kyoto University (Author)
  • Masamitsu Sone - , Kyoto University (Author)
  • Makito Koga - , RIKEN Center for Developmental Biology (Author)
  • Miki Ebisuya - , Chair of Cell and Tissue Control, Clusters of Excellence PoL: Physics of Life, RIKEN Center for Developmental Biology (Author)
  • Takuya Yamamoto - , Kyoto University (Author)
  • Eisuke Nishida - , Kyoto University (Author)

Abstract

The role of secreted molecules in cellular reprogramming has been poorly understood. Here we identify a truncated form of ephrin receptor A7 (EPHA7) as a key regulator of reprogramming. Truncated EPHA7 is prominently upregulated and secreted during reprogramming. EPHA7 expression is directly regulated by OCT3/4. EphA7 knockdown results in marked reduction of reprogramming efficiency, and the addition of truncated EPHA7 is able to restore it. ERK activity is markedly reduced during reprogramming, and the secreted, truncated EPHA7 is responsible for ERK activity reduction. Remarkably, treatment of EphA7-knockdown MEFs with the ERK pathway inhibitor restores reprogramming efficiency. Analyses show that truncated EPHA7-induced ERK activity reduction plays an important role in the middle phase of reprogramming. Thus, our findings uncover the importance of secreted EPHA7-induced ERK activity reduction in reprogramming.

Details

Original languageEnglish
Pages (from-to)480-9
Number of pages10
JournalStem cell reports
Volume5
Issue number4
Publication statusPublished - 13 Oct 2015
Peer-reviewedYes

External IDs

PubMedCentral PMC4625027
Scopus 84944394663

Keywords

Keywords

  • Animals, Cells, Cultured, Cellular Reprogramming, Fibroblasts/cytology, Gene Knockdown Techniques, HEK293 Cells, Humans, MAP Kinase Signaling System, Mice, Mice, Inbred ICR, Receptor, EphA7/genetics