BMP2, but not BMP4, is crucial for chondrocyte proliferation and maturation during endochondral bone development

Bing Shu, Ming Zhang, Rong Xie, Meina Wang, Hongting Jin, Wei Hou, Dezhi Tang, Stephen E Harris, Yuji Mishina, Regis J. O'Keefe, Matthew J. Hilton, Yongjun Wang, Di Chen

Research output: Contribution to journalArticle

108 Citations (Scopus)

Abstract

The BMP signaling pathway has a crucial role in chondrocyte proliferation and maturation during endochondral bone development. To investigate the specific function of the Bmp2 and Bmp4 genes in growth plate chondrocytes during cartilage development, we generated chondrocyte-specific Bmp2 and Bmp4 conditional knockout (cKO) mice and Bmp2, Bmp4 double knockout (dKO) mice. We found that deletion of Bmp2 and Bmp4 genes or the Bmp2 gene alone results in a severe chondrodysplasia phenotype, whereas deletion of the Bmp4 gene alone produces a minor cartilage phenotype. Both dKO and Bmp2 cKO mice exhibit severe disorganization of chondrocytes within the growth plate region and display profound defects in chondrocyte proliferation, differentiation and apoptosis. To understand the mechanism by which BMP2 regulates these processes, we explored the specific relationship between BMP2 and Runx2, a key regulator of chondrocyte differentiation. We found that BMP2 induces Runx2 expression at both the transcriptional and post-transcriptional levels. BMP2 enhances Runx2 protein levels through inhibition of CDK4 and subsequent prevention of Runx2 ubiquitylation and proteasomal degradation. Our studies provide novel insights into the genetic control and molecular mechanism of BMP signaling during cartilage development.

Original languageEnglish (US)
Pages (from-to)3428-3440
Number of pages13
JournalJournal of Cell Science
Volume124
Issue number20
DOIs
StatePublished - Oct 2011

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Bone Development
Chondrocytes
Knockout Mice
Cartilage
Growth Plate
Core Binding Factor Alpha 1 Subunit
Enchondromatosis
Genes
Phenotype
Ubiquitination
Gene Deletion
Molecular Biology
Apoptosis

Keywords

  • Bmp2
  • Bmp4
  • Chondrocyte
  • Endochondral bone formation

ASJC Scopus subject areas

  • Cell Biology

Cite this

BMP2, but not BMP4, is crucial for chondrocyte proliferation and maturation during endochondral bone development. / Shu, Bing; Zhang, Ming; Xie, Rong; Wang, Meina; Jin, Hongting; Hou, Wei; Tang, Dezhi; Harris, Stephen E; Mishina, Yuji; O'Keefe, Regis J.; Hilton, Matthew J.; Wang, Yongjun; Chen, Di.

In: Journal of Cell Science, Vol. 124, No. 20, 10.2011, p. 3428-3440.

Research output: Contribution to journalArticle

Shu, B, Zhang, M, Xie, R, Wang, M, Jin, H, Hou, W, Tang, D, Harris, SE, Mishina, Y, O'Keefe, RJ, Hilton, MJ, Wang, Y & Chen, D 2011, 'BMP2, but not BMP4, is crucial for chondrocyte proliferation and maturation during endochondral bone development', Journal of Cell Science, vol. 124, no. 20, pp. 3428-3440. https://doi.org/10.1242/jcs.083659
Shu, Bing ; Zhang, Ming ; Xie, Rong ; Wang, Meina ; Jin, Hongting ; Hou, Wei ; Tang, Dezhi ; Harris, Stephen E ; Mishina, Yuji ; O'Keefe, Regis J. ; Hilton, Matthew J. ; Wang, Yongjun ; Chen, Di. / BMP2, but not BMP4, is crucial for chondrocyte proliferation and maturation during endochondral bone development. In: Journal of Cell Science. 2011 ; Vol. 124, No. 20. pp. 3428-3440.
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