CNRS, INRAe, Physiologie de la Reproduction et des Comportements, 37380 Nouzilly, France.
Faculty of Natural Sciences, Quy Nhon University, Quy Nhon 820000, Vietnam.
Int J Mol Sci. 2021 Apr 28;22(9):4641. doi: 10.3390/ijms22094641.
In contrast to all transmembrane adenylyl cyclases except ADCY9, the cytosolic soluble adenylyl cyclase (ADCY10) is insensitive to forskolin stimulation and is uniquely modulated by calcium and bicarbonate ions. In the present paper, we focus on ADCY10 localization and a kinetic analysis of intracellular cAMP accumulation in response to human LH in the absence or presence of four different ADCY10 inhibitors (KH7, LRE1, 2-CE and 4-CE) in MTLC-1 cells. ADCY10 was immuno-detected in the cytoplasm of MLTC-1 cells and all four inhibitors were found to inhibit LH-stimulated cAMP accumulation and progesterone level in MLTC-1 and testosterone level primary Leydig cells. Interestingly, similar inhibitions were also evidenced in mouse testicular Leydig cells. In contrast, the tmAC-specific inhibitors ddAdo3' and ddAdo5', even at high concentration, exerted weak or no inhibition on cAMP accumulation, suggesting an important role of ADCY10 relative to tmACs in the MLTC-1 response to LH. The strong synergistic effect of HCO under LH stimulation further supports the involvement of ADCY10 in the response to LH.
与除了 ADCY9 以外的所有跨膜腺苷酸环化酶不同,细胞质可溶性腺苷酸环化酶(ADCY10)对福司可林刺激不敏感,并且被钙离子和碳酸氢根离子独特地调节。在本文中,我们专注于 ADCY10 的定位以及在 MTLC-1 细胞中缺乏或存在四种不同的 ADCY10 抑制剂(KH7、LRE1、2-CE 和 4-CE)时对人 LH 反应的细胞内 cAMP 积累的动力学分析。ADCY10 在 MLTC-1 细胞的细胞质中被免疫检测到,并且发现这四种抑制剂均能抑制 LH 刺激的 cAMP 积累和 MLTC-1 中的孕激素水平以及原代睾丸间质细胞中的睾酮水平。有趣的是,在小鼠睾丸间质细胞中也证实了类似的抑制作用。相比之下,tmAC 特异性抑制剂 ddAdo3'和 ddAdo5',即使在高浓度下,对 cAMP 积累的抑制作用也很弱或没有,这表明相对于 tmACs,ADCY10 在 MLTC-1 对 LH 的反应中起着重要作用。在 LH 刺激下 HCO 的强烈协同作用进一步支持了 ADCY10 参与 LH 反应。