Direct reprogramming of fibroblasts into smooth muscle-like cells with defined transcription factors-brief report

Hiroyuki Hirai, Bo Yang, Minerva T. Garcia-Barrio, Oren Rom, Peter X. Ma, Jifeng Zhang, Y. Eugene Chen

Research output: Contribution to journalArticle

6 Scopus citations

Abstract

Objective-To identify the transcription factors that could contribute to direct reprogramming of fibroblasts toward smooth muscle cell fate. Approach and Results-We screened various combinations of transcription factors, including Myocd (myocardin), Mef2C (myocyte enhancer factor 2C), Mef2B (myocyte enhancer factor 2B), Mkl1 (MKL [megakaryoblastic leukemia]/Myocdlike 1), Gata4 (GATA-binding protein 4), Gata5 (GATA-binding protein 5), Gata6 (GATA-binding protein 6), Ets1 (E26 avian leukemia oncogene 1, 5' domain), and their corresponding carboxyterminal fusions to the transactivation domain of MyoD (myogenic differentiation 1)-indicated by∗-for their effects on reprogramming mouse embryonic fibroblasts and human adult dermal fibroblasts to the smooth muscle cell fate as determined by the expression of specific markers. The combination of 3 transcription factors, Myocd (or Myocd∗) with Mef2C (or Mef2C∗) and Gata6, was the most efficient in enhancing the expression of smooth muscle marker genes and decreasing fibroblast gene expression. Additionally, the derived induced smooth muscle-like cells showed a contractile phenotype in response to carbachol. Conclusions-Combination of Myocd and Gata6 with Mef2C∗(MG2∗) could sufficiently and efficiently direct differentiation of mouse embryonic and human dermal fibroblasts into induced smooth muscle-like cells, thus opening new opportunities for disease modeling, tissue engineering, and personalized medicine.

Original languageEnglish (US)
Pages (from-to)2191-2197
Number of pages7
JournalArteriosclerosis, thrombosis, and vascular biology
Volume38
Issue number9
DOIs
StatePublished - 2018

Keywords

  • animals
  • humans
  • mice
  • myocytes, smooth muscle
  • phenotype

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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