Open AccessTransforming growth factor β controls CCN3 expression in nucleus pulposus cells of the intervertebral disc
Author(s) -
Tran Cassie M.,
Smith Harvey E.,
Symes Aviva,
Rittié Laure,
Perbal Bernard,
Shapiro Irving M.,
Risbud Makarand V.
Publication year - 2011
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.30468
Subject(s) - versican , nucleus , transforming growth factor , chemistry , gene knockdown , microbiology and biotechnology , transforming growth factor beta , aggrecan , small interfering rna , extracellular matrix , biology , transfection , proteoglycan , medicine , pathology , gene , articular cartilage , biochemistry , alternative medicine , osteoarthritis
Objective To investigate transforming growth factor β (TGFβ) regulation of CCN3 expression in cells of the nucleus pulposus. Methods Real‐time reverse transcription–polymerase chain reaction and Western blot analyses were used to measure CCN3 expression in the nucleus pulposus. Transfections were used to measure the effect of Smad3, MAPKs, and activator protein 1 (AP‐1) on TGFβ‐mediated CCN3 promoter activity. Lentiviral knockdown of Smad3 was performed to assess the role of Smad3 in CCN3 expression. Results CCN3 was expressed in embryonic and adult intervertebral discs. TGFβ decreased the expression of CCN3 and suppressed its promoter activity in nucleus pulposus cells. DN‐Smad3, Smad3 small interfering RNA, or DN‐AP‐1 had little effect on TGFβ suppression of CCN3 promoter activity. However, p38 and ERK inhibitors blocked suppression of CCN3 by TGFβ, suggesting involvement of these signaling pathways in the regulation of CCN3. Interestingly, overexpression of Smad3 in the absence of TGFβ increased CCN3 promoter activity. We validated the role of Smad3 in controlling CCN3 expression in Smad3‐null mice and in nucleus pulposus cells transduced with lentiviral short hairpin Smad3. In terms of function, treatment with recombinant CCN3 showed a dose‐dependent decrease in the proliferation of nucleus pulposus cells. Moreover, CCN3‐treated cells showed a decrease in aggrecan, versican, CCN2, and type I collagen expression. Conclusion The opposing effect of TGFβ on CCN2 and CCN3 expression and the suppression of CCN2 by CCN3 in nucleus pulposus cells further the paradigm that these CCN proteins form an interacting triad, which is possibly important in maintaining extracellular matrix homeostasis and cell numbers.