4.5 Article

Elimination of BMP7 from the developing limb mesenchyme leads to articular cartilage degeneration and synovial inflammation with increased age

Journal

FEBS LETTERS
Volume 589, Issue 11, Pages 1240-1248

Publisher

WILEY
DOI: 10.1016/j.febslet.2015.04.004

Keywords

Bone morphogenetic protein 7; Articular cartilage; Synovitis; Proteoglycan; Activin A; Osteoarthritis

Funding

  1. Japan Society for the Promotion of Science (JSPS)
  2. Japan Ministry of Education, Culture, Sports, Science, and Technology
  3. Global Center of Excellence (GCOE) Program, International Research Center for Molecular Science in Tooth and Bone Diseases
  4. Pfizer Academic Contributions
  5. Grants-in-Aid for Scientific Research [15K10464, 26462287, 25460716, 25293317] Funding Source: KAKEN

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While osteo- and chondro-inductive activities of recombinant human bone morphogenetic protein 7 are well established, evaluation of the role of endogenous BMP7 in skeletal homeostasis has been hampered by perinatal lethality in BMP7 knockout mice. Here, we examined physiological roles of endogenous BMP7 in joint homeostasis and showed that proteoglycan contents in articular cartilage were significantly reduced in the absence of BMP7. Loss of BMP7 did not affect survival of articular cartilage cells, but resulted in reduced expression of aggrecan and enhanced expression of matrix metalloproteinase 13. We also found extensive synovial hyperplasia and enhanced expression of Activin A. These findings suggest that locally produced BMP7 is prerequisite for postnatal synovial joint homeostasis and may be involved in osteoarthritic changes in adults. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

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