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Regulation of gene expression by NFAT transcription factors in hibernating ground squirrels is dependent on the cellular environment

机译:NFAT转录因子在冬松鼠冬眠中对基因表达的调控取决于细胞环境

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Calcineurin is a calmodulin-stimulated phosphatase that regulates the nuclear translocation of nuclear factor of activated T cell (NFAT) c1-4 through dephosphorylation. We believe that this mechanism plays various roles in the remodeling and maintenance of Ictidomys tridecemlineatus skeletal muscle. During hibernation, bouts of torpor and arousal take place, and squirrels do not lose muscle mass despite being inactive. Protein expression of Ca2+ signaling proteins were studied using immunoblotting. A DNA-protein interaction ELISA technique was created to test the binding of NFATs in the nucleus to DNA probes containing the NFAT response element under environmental conditions reflective of those during hibernation. Calcineurin protein levels increased by 3.08-fold during torpor (compared to euthermic control), whereas calpain1 levels also rose by 3.66-fold during torpor. Calmodulin levels were elevated upon entering torpor. NFATc4 binding to DNA showed a 1.4-fold increase during torpor, and we found that this binding was further enhanced when 600?nM of Ca2+ was supplemented. We also found that decreasing the temperature of ELISAs resulted in progressive decreases in the binding of NFATs c1, c3, and c4 to DNA. In summary, calmodulin and calpain1 appear to activate calcineurin and NFATc4 during torpor. NFAT binding to target promoters is affected by intranuclear [Ca2+] and environmental temperatures. Therefore, Ca2+ signaling and temperature changes play key roles in regulation of the NFAT-calcineurin pathway in skeletal muscle of hibernating 13-lined ground squirrels over the torpor-arousal cycle, and they may contribute to the avoidance of disuse-induced muscle atrophy that occurs naturally in these animals.
机译:钙调神经磷酸酶是钙调蛋白刺激的磷酸酶,它通过去磷酸化调节活化T细胞(NFAT)c1-4的核因子的核转运。我们认为,该机制在Ictidomys tridecemlineatus骨骼肌的重塑和维持中起着多种作用。在冬眠期间,会发生to打和唤醒,并且即使不活动,松鼠也不会失去肌肉质量。使用免疫印迹研究了Ca2 +信号蛋白的蛋白表达。建立了一种DNA-蛋白质相互作用ELISA技术,以在反映休眠状态的环境条件下测试细胞核中NFAT与含有NFAT反应元件的DNA探针的结合。钙调磷酸酶蛋白水平在torpor期间增加了3.08倍(与正常控制相比),而calcain1水平在torpor期间也增加了3.66倍。进入玉米粥后钙调蛋白水平升高。 NFATc4与DNA的结合在玉米粉蒸煮过程中增加了1.4倍,我们发现当补充600?nM Ca2 +时,这种结合会进一步增强。我们还发现降低ELISA温度会导致NFAT c1,c3和c4与DNA的结合逐渐减少。总而言之,钙调蛋白和钙蛋白酶1似乎在玉米粥中激活钙调神经磷酸酶和NFATc4。 NFAT与靶标启动子的结合受核内[Ca2 +]和环境温度的影响。因此,Ca2 +信号传导和温度变化在冬眠的13个内衬松鼠的骨骼肌中NFAT-calcineurin通路的调节中起着关键作用,在冬眠周期中,它们可能有助于避免因滥用引起的肌肉萎缩在这些动物中自然。

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