Watt V M, Schimmer B P
J Biol Chem. 1982 Feb 25;257(4):1684-9.
Adrenocorticotropin(ACTH)-induced desensitization of adenylate cyclase was examined in subclones derived from the ACTH-responsive, Y1 mouse adrenocortical tumor cell line. This report describes clonal variation in ACTH-induced desensitization of adenylate cyclase and an associated variation in the level of a 68,000-dalton protein, p68. A subclone of Y1 cells with a low level of p68 (0.8% of total protein) exhibited a faster rate of desensitization and a slower rate of recovery from desensitization when compared with a clone containing a high level of p68 (10% of total protein). In three clones with low levels of p68, ACTH desensitized adenylate cyclase with ED50 values from 0.3 to 0.5 nM. In several clones with high levels of p68, the adenylate cyclase system was more resistant to ACTH-induced desensitization; the ED50 values for ACTH in these clones ranged from 2 to 12 nM. Among 11 ACTH-responsive subclones, the level of p68 correlated significantly (p less than 0.001, r = 0.87) with resistance to the desensitization induced by 1 nM ACTH. These results suggest that p68 may function in the maintenance of an ACTH-responsive adenylate cyclase system, or that the level of p68 and responsiveness to ACTH are coordinately regulated.
在源自促肾上腺皮质激素(ACTH)反应性Y1小鼠肾上腺皮质肿瘤细胞系的亚克隆中,研究了ACTH诱导的腺苷酸环化酶脱敏作用。本报告描述了ACTH诱导的腺苷酸环化酶脱敏作用中的克隆变异以及一种68,000道尔顿蛋白p68水平的相关变异。与含有高水平p68(占总蛋白的10%)的克隆相比,p68水平低(占总蛋白的0.8%)的Y1细胞亚克隆表现出更快的脱敏速率和更慢的脱敏恢复速率。在三个p68水平低的克隆中,ACTH使腺苷酸环化酶脱敏的ED50值为0.3至0.5 nM。在几个p68水平高的克隆中,腺苷酸环化酶系统对ACTH诱导的脱敏作用更具抗性;这些克隆中ACTH的ED50值范围为2至12 nM。在11个ACTH反应性亚克隆中,p68水平与对1 nM ACTH诱导的脱敏作用的抗性显著相关(p小于0.001,r = 0.87)。这些结果表明,p68可能在维持ACTH反应性腺苷酸环化酶系统中发挥作用,或者p68水平与对ACTH的反应性受到协同调节。