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Activation of Wnt Planar cell polarity (PCP) signaling promotes growth plate column formation in vitro
Author(s) -
Randall Rachel M.,
Shao Yvonne Y.,
Wang Lai,
Ballock R. Tracy
Publication year - 2012
Publication title -
journal of orthopaedic research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.041
H-Index - 155
eISSN - 1554-527X
pISSN - 0736-0266
DOI - 10.1002/jor.22152
Subject(s) - wnt signaling pathway , microbiology and biotechnology , cell polarity , chondrocyte , frizzled , cell growth , chemistry , morphogenesis , lrp5 , biology , cell , signal transduction , in vitro , biochemistry , gene
Disrupting the Wnt Planar Cell Polarity (PCP) signaling pathway in vivo results in loss of columnar growth plate architecture, but it is unknown whether activation of this pathway in vitro is sufficient to promote column formation. We hypothesized that activation of the Wnt PCP pathway in growth plate chondrocyte cell pellets would promote columnar organization in these cells that are normally oriented randomly in culture. Rat growth plate chondrocytes were transfected with plasmids encoding the Fzd7 cell‐surface Wnt receptor, a Fzd7 deletion mutant lacking the Wnt‐binding domain, or Wnt receptor‐associated proteins Ror2 or Vangl2, and then cultured as three‐dimensional cell pellets in the presence of recombinant Wnt5a or Wnt5b for 21 days. Cellular morphology was evaluated using histomorphometric measurements. Activation of Wnt PCP signaling components promoted the initiation of columnar morphogenesis in the chondrocyte pellet culture model, as measured by histomorphometric analysis of the column index (ANOVA p = 0.01). Activation of noncanonical Wnt signaling through overexpression of both the cell‐surface Wnt receptor Fzd7 and receptor‐associated protein Ror2 with addition of recombinant Wnt5a promotes the initiation of columnar architecture of growth plate chondrocytes in vitro, representing an important step toward growth plate regeneration. © 2012 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 30:1906–1914, 2012