Research Laboratory of Cell Regulation, Shanghai Jiaotong University School of Medicine, Shanghai, China.
FEBS Lett. 2010 Apr 16;584(8):1549-52. doi: 10.1016/j.febslet.2010.03.006. Epub 2010 Mar 6.
This work studied the role of cyclic AMP responsive element binding protein (CREB) in the up-regulation of M(1) muscarinic acetylcholine receptor (M(1) receptor) density by sarsasapogenin (ZMS) in CHO cells transfected with M(1) receptor gene (CHOm1 cells). During cell aging, sarsasapogenin elevated M(1) receptor density as well as CREB and phosphor-CREB (pCREB) levels. CREB peaked earliest, followed by pCREB and M(1) receptor density peaked last. When CREB synthesis was blocked by antisense oligonucleotides, the elevation effect of sarsasapogenin on M(1) receptor density was abolished. These results suggest that sarsasapogenin up-regulates M(1) receptor density in aged cells by promoting CREB production and phosphorylation. Furthermore, the results support the hypothesis that pCREB regulates M(1) receptor gene expression through heterodimer formation.
这项工作研究了环状 AMP 反应元件结合蛋白(CREB)在芝麻素(ZMS)上调转染 M1 受体基因(CHOm1 细胞)的 CHO 细胞中 M1 毒蕈碱乙酰胆碱受体(M1 受体)密度中的作用。在细胞衰老过程中,芝麻素升高了 M1 受体密度以及 CREB 和磷酸化 CREB(pCREB)水平。CREB 最早达到峰值,其次是 pCREB,最后是 M1 受体密度达到峰值。当使用反义寡核苷酸阻断 CREB 合成时,芝麻素对 M1 受体密度的升高作用被消除。这些结果表明,芝麻素通过促进 CREB 的产生和磷酸化来上调衰老细胞中的 M1 受体密度。此外,这些结果支持 pCREB 通过形成异二聚体来调节 M1 受体基因表达的假说。