Department of Cell Biology, Center for Research and Advanced Studies-IPN, Apdo. Postal 14-740, México City 07000, Mexico.
Biochem Biophys Res Commun. 2013 Mar 1;432(1):146-51. doi: 10.1016/j.bbrc.2013.01.069. Epub 2013 Feb 1.
The endothelial differentiation factor-1 (EDF-1) is a calmodulin binding protein that regulates calmodulin-dependent enzymes. In endothelial cells, this factor can form a protein complex with calmodulin. We analyzed the relationship between this factor and the members of calmodulin/calcineurin/nuclear factor of activated T-cells (NFAT) signaling pathway during adipogenesis of 3T3-F442A cells. We found that the expression of edf1 is upregulated during early adipogenesis, whereas that of calcineurin gene is lowered, suggesting that this pathway should be downregulated to allow for adipogenesis to occur. We also found that EDF-1 associates with calmodulin and calcineurin, most likely inactivating calcineurin. Our results showed that EDF-1 inactivates the calmodulin/calcineurin/NFAT pathway via sequestration of calmodulin, during early adipogenesis, and we propose a mechanism that negatively regulates the activation of calcineurin through a complex formation between EDF-1 and calmodulin. This finding raises the possibility that modulating this pathway might offer some alternatives to regulate adipose biology.
内皮分化因子-1(EDF-1)是一种钙调蛋白结合蛋白,可调节钙调蛋白依赖性酶。在内皮细胞中,该因子可以与钙调蛋白形成蛋白复合物。在 3T3-F442A 细胞的脂肪生成过程中,我们分析了该因子与钙调蛋白/钙调磷酸酶/活化 T 细胞核因子(NFAT)信号通路成员之间的关系。我们发现,edf1 的表达在早期脂肪生成过程中上调,而钙调磷酸酶基因的表达降低,表明该途径应下调以允许脂肪生成发生。我们还发现,EDF-1 与钙调蛋白和钙调磷酸酶结合,很可能使钙调磷酸酶失活。我们的结果表明,EDF-1 通过钙调蛋白的隔离在早期脂肪生成过程中使钙调蛋白/钙调磷酸酶/NFAT 途径失活,我们提出了一种通过 EDF-1 与钙调蛋白形成复合物来负调控钙调磷酸酶激活的机制。这一发现提出了一种可能性,即调节该途径可能为调节脂肪生物学提供一些替代方案。