Journal of Cellular Biochemistry

Retinoic acid and the transcription factor MafB act together and differentially to regulate aggrecan and matrix metalloproteinase gene expression in neonatal chondrocytes§

Authors

  • Yao Zhang,

    1. Department of Nutritional Sciences, Pennsylvania State University, University Park, Pennsylvania 16802
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  • Dr. A. Catharine Ross PhD

    Corresponding author
    1. Department of Nutritional Sciences, Pennsylvania State University, University Park, Pennsylvania 16802
    2. Center of Molecular Immunology and Infectious Disease, Pennsylvania State University, University Park, Pennsylvania 16802
    • 110 Chandlee Laboratory, University Park, PA 16802.
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  • All authors state that they have no conflicts of interest.

  • Materials disclosure: Information about the materials and methods used is available from Dr. Ross. No permanent new materials or models were generated.

  • §

    Author's contribution: Study design, conduct, data interpretation, and manuscript preparation: Y.Z. and A.C.R. A.C.R. takes responsibility for the integrity of the data analysis.

Abstract

Vitamin A (VA) and its active form, retinoic acid (RA), are regulators of skeletal development and chondrogenesis. MafB, a transcription factor, has been identified as an important mediator in monocyte and osteoclast differentiation. However, the presence and function of MafB in chondrocytes is not clear. In this study, MafB gene expression was regulated by both the VA status of the mother (VA-marginal, adequate, and supplemented diets) and by direct oral supplementation of the neonates with VARA (VA mixed with 10% RA). Expression was highest in neonates of VA-supplemented versus VA-marginal dams (P < 0.05), and in VARA-treated versus placebo-treated neonates across all diet groups (P < 0.05). To examine cellular changes, primary chondrocytes derived from neonatal rat ribs were cultured in the presence of RA for up to 48 h. MafB mRNA exhibited a time- and dose-dependent increase in response to RA, while the induction of MafB mRNA was attenuated by BMS-493, a pan-RAR inverse agonist, implicating RAR signaling in the regulation of MafB. The genetic knockdown of MafB in chondrocytes using siRNA (MafBSI chondrocytes) abrogated the RA-induced increase in MafB expression. MafBSI chondrocytes expressed higher levels of aggrecan mRNA. Additionally, the increased matrix metalloproteinase (MMP)3 and MMP13 gene expression due to RA was attenuated in MafBSI chondrocytes, while total extracellular matrix staining was increased. These results support a role for MafB as a regulator of chondrocyte gene expression and matrix formation via control of aggrecan, MMP3 and MMP13 expression, and indicate an important role for RA in the regulation of MafB. J. Cell. Biochem. 114: 471–479, 2013. © 2012 Wiley Periodicals, Inc.

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