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Creb5 coordinates synovial joint formation with the genesis of articular cartilage

Author

Listed:
  • Cheng-Hai Zhang

    (Blavatnik Institute at Harvard Medical School)

  • Yao Gao

    (Blavatnik Institute at Harvard Medical School)

  • Han-Hwa Hung

    (Massachusetts Institute of Technology)

  • Zhu Zhuo

    (Harvard T.H. Chan School of Public Health)

  • Alan J. Grodzinsky

    (Massachusetts Institute of Technology)

  • Andrew B. Lassar

    (Blavatnik Institute at Harvard Medical School)

Abstract

While prior work has established that articular cartilage arises from Prg4-expressing perichondrial cells, it is not clear how this process is specifically restricted to the perichondrium of synovial joints. We document that the transcription factor Creb5 is necessary to initiate the expression of signaling molecules that both direct the formation of synovial joints and guide perichondrial tissue to form articular cartilage instead of bone. Creb5 promotes the generation of articular chondrocytes from perichondrial precursors in part by inducing expression of signaling molecules that block a Wnt5a autoregulatory loop in the perichondrium. Postnatal deletion of Creb5 in the articular cartilage leads to loss of both flat superficial zone articular chondrocytes coupled with a loss of both Prg4 and Wif1 expression in the articular cartilage; and a non-cell autonomous up-regulation of Ctgf. Our findings indicate that Creb5 promotes joint formation and the subsequent development of articular chondrocytes by driving the expression of signaling molecules that both specify the joint interzone and simultaneously inhibit a Wnt5a positive-feedback loop in the perichondrium.

Suggested Citation

  • Cheng-Hai Zhang & Yao Gao & Han-Hwa Hung & Zhu Zhuo & Alan J. Grodzinsky & Andrew B. Lassar, 2022. "Creb5 coordinates synovial joint formation with the genesis of articular cartilage," Nature Communications, Nature, vol. 13(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-35010-0
    DOI: 10.1038/s41467-022-35010-0
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