Barber R
Mol Cell Endocrinol. 1986 Aug;46(3):263-70. doi: 10.1016/0303-7207(86)90008-0.
The relationship between epinephrine-induced receptor-epinephrine affinity changes and intact cell adenylate cyclase activity was investigated using S49 lymphoma cells. It was demonstrated that 20 nM epinephrine caused desensitization (defined as a reduction in the rate of cAMP synthesis with time), but no significant change in receptor-epinephrine affinity as measured by competition with [125I]iodopindolol. On the other hand, treatment with 5 microM epinephrine caused no desensitization (as defined above), but did cause a very significant reduction in receptor-epinephrine affinity. It is suggested that there is a desensitization process which is distinct from the agonist affinity shift and which is expressed primarily as a change in the EC50 of the hormone-induced activation. The demonstration of extensive desensitization at low concentrations of hormone may have important physiological implications.
利用S49淋巴瘤细胞研究了肾上腺素诱导的受体 - 肾上腺素亲和力变化与完整细胞腺苷酸环化酶活性之间的关系。结果表明,20 nM肾上腺素引起脱敏作用(定义为cAMP合成速率随时间降低),但用[125I]碘吲哚洛尔竞争法测定时,受体 - 肾上腺素亲和力无显著变化。另一方面,用5 microM肾上腺素处理未引起脱敏作用(如上所定义),但确实导致受体 - 肾上腺素亲和力非常显著降低。提示存在一种与激动剂亲和力改变不同的脱敏过程,其主要表现为激素诱导激活的EC50变化。低浓度激素时广泛脱敏作用的证明可能具有重要的生理学意义。