García-Higuera I, Mayor F
Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Universidad Autónoma, Madrid, Spain.
J Clin Invest. 1994 Mar;93(3):937-43. doi: 10.1172/JCI117099.
Exposure of beta-adrenergic receptors (BAR) to agonists often leads to a rapid loss of receptor responsiveness. The proposed mechanisms of such rapid receptor desensitization include receptor phosphorylation by either cAMP-dependent protein kinase or the specific beta-adrenergic receptor kinase (BARK), leading to functional uncoupling from adenylyl cyclase and sequestration of the receptors away from the cell surface. To evaluate the physiological role of such mechanisms, we have investigated whether rapid regulation of BAR occurs in the neonatal rat liver immediately after birth, a physiological situation characterized by a dramatic but transient increase in plasma catecholamines. We have detected a rapid, transient uncoupling of liver plasma membrane BARs from adenylyl cyclase (corresponding to a desensitization of approximately 45%) within the first minutes of extrauterine life, followed by a transient sequestration of approximately 40% of the BARs away from the plasma membrane. In agreement with such pattern of desensitization, we have detected (by enzymatic and immunological assays) rapid changes in BARK specific activity in different neonatal rat liver subcellular fractions that take place within the same time frame of BAR uncoupling and sequestration. Our results provide new evidence on the potential role of BAR desensitization mechanisms in vivo and suggest that they are involved in modulating catecholamines actions at the moment of birth. Furthermore, our data indicate that in addition to its suggested role as a rapid modulator of adrenergic receptor function at synapse, rapid BARK-mediated receptor regulation may have functional relevance in other tissues in response to high circulating or local levels of agonists.
β-肾上腺素能受体(BAR)暴露于激动剂常常导致受体反应性迅速丧失。这种快速受体脱敏的推测机制包括由环磷酸腺苷(cAMP)依赖性蛋白激酶或特异性β-肾上腺素能受体激酶(BARK)介导的受体磷酸化,导致与腺苷酸环化酶功能解偶联以及受体从细胞表面内陷。为了评估这些机制的生理作用,我们研究了出生后即刻新生大鼠肝脏中BAR是否发生快速调节,这是一种以血浆儿茶酚胺急剧但短暂增加为特征的生理状态。我们检测到宫外生活的最初几分钟内,肝细胞膜BAR与腺苷酸环化酶迅速、短暂解偶联(相当于约45%的脱敏),随后约40%的BAR从细胞膜内陷。与这种脱敏模式一致,我们通过酶学和免疫学检测发现,不同新生大鼠肝脏亚细胞组分中BARK比活性在与BAR解偶联和内陷相同的时间框架内发生快速变化。我们的结果为BAR脱敏机制在体内的潜在作用提供了新证据,并表明它们在出生时参与调节儿茶酚胺的作用。此外,我们的数据表明,除了其作为突触处肾上腺素能受体功能快速调节剂的推测作用外,快速的BARK介导的受体调节可能在其他组织中对高循环或局部激动剂水平有功能相关性。