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Biochem Biophys Res Commun. 2005;327(3):811-9.

Ectopic overexpression of adipogenic transcription factors induces transdifferentiation of MC3T3-E1 osteoblasts.

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제1저자 김상완 · 교신저자 신찬수

PMID 15649418 DOI 10.1016/j.bbrc.2004.12.076 IF 2.5 내분비대사내과
소속 (1)
  1. Department of Internal Medicine, Seoul National University College of Medicine, 28 Yungun-Dong, Chongno-Gu, Seoul 110-744, Republic of Korea.

Abstract

Osteoblasts and adipocytes originate from common mesenchymal progenitor cells. We have investigated whether mouse osteoblastic MC3T3-E1 cells can be induced to transdifferentiate into mature adipocytes by the ectopic expression of adipogenic transcription factors, PPARgamma, C/EBPalpha, or both. Retrovirus-mediated overexpression of PPARgamma alone or both PPARgamma and C/EBPalpha resulted in reduced alkaline phosphatase activity and osteoblast-specific gene expression. Moreover, foci of adipocytes were identified in conditions favoring osteoblastic maturation. Upon treatment with insulin, dexamethasone, and IBMX, cells overexpressing PPARgamma alone or both PPARgamma and C/EBPalpha showed marked transdifferentiation to mature adipocytes expressing molecular markers of adipocytes. Cells expressing both PPARgamma and C/EBPalpha showed more robust phenotype of adipocytes than the cells expressing PPARgamma alone. Overexpression of C/EBPalpha alone did not result in adipogenesis. These results suggest that PPARgamma is a key molecular switch for the transdifferentiation to adipocytes whereas C/EBPalpha may differentiate MC3T3-E1 cells into osteoblasts and adipocytes.

그 밖의 정보
출판 형태
Journal Article, Research Support, Non-U.S. Gov't
저널
Biochemical and biophysical research communications · ISSN 0006-291X
MeSH
1-Methyl-3-isobutylxanthine / pharmacology · 3T3 Cells · Adipocytes / metabolism · Alkaline Phosphatase / metabolism · Animals · Base Sequence · CCAAT-Enhancer-Binding Protein-alpha / metabolism · Cell Differentiation / physiology · Cells, Cultured · Dexamethasone / pharmacology · Gene Expression Regulation · Insulin / metabolism · Mice · Osteoblasts / cytology · PPAR gamma / metabolism · Phenotype · Transcription Factors / genetics / physiology
Substances
CCAAT-Enhancer-Binding Protein-alpha · Insulin · PPAR gamma · Transcription Factors · Dexamethasone · Alkaline Phosphatase · 1-Methyl-3-isobutylxanthine