Tomita Masuhiro, Reinhold Martina I, Molkentin Jeffery D, Naski Michael C
Department of Pathology, University of Texas Health Science Center, San Antonio 78229, USA.
J Biol Chem. 2002 Nov 1;277(44):42214-8. doi: 10.1074/jbc.C200504200. Epub 2002 Sep 17.
Nuclear factor of activated T-cells (NFAT) and calcineurin are essential regulators of immune cell and mesenchymal cell differentiation. Here we show that elevated intracellular calcium induces chondrogenesis through a calcineurin/NFAT signaling axis that activates bone morphogenetic protein (BMP) expression. The calcium ionophore, ionomycin, induced chondrogenesis through activation of calcineurin. The calcineurin substrate, NFAT4, also induced chondrogenesis and chondrocyte gene expression. Significantly, the BMP antagonist, noggin, or dominant negative BMP receptors blocked the effects of elevated intracellular calcium on chondrogenesis. This suggested that calcineurin/NFAT4 activates BMP expression. Consistent with this, BMP2 gene expression was increased by ionomycin and suppressed by the calcineurin inhibitor, cyclosporine A. Furthermore, activated NFAT4 induced BMP2 gene expression. These results have important implications for the effects of NFATs during development and adaptive responses.
活化T细胞核因子(NFAT)和钙调神经磷酸酶是免疫细胞和间充质细胞分化的关键调节因子。在此我们表明,细胞内钙水平升高通过激活骨形态发生蛋白(BMP)表达的钙调神经磷酸酶/NFAT信号轴诱导软骨形成。钙离子载体离子霉素通过激活钙调神经磷酸酶诱导软骨形成。钙调神经磷酸酶底物NFAT4也诱导软骨形成和软骨细胞基因表达。重要的是,BMP拮抗剂头蛋白或显性负性BMP受体阻断了细胞内钙水平升高对软骨形成的影响。这表明钙调神经磷酸酶/NFAT4激活BMP表达。与此一致,离子霉素增加了BMP2基因表达,而钙调神经磷酸酶抑制剂环孢素A抑制了该表达。此外,活化的NFAT4诱导BMP2基因表达。这些结果对于NFATs在发育和适应性反应中的作用具有重要意义。