Teitelbaum I
University of Colorado School of Medicine, Denver 80262.
Am J Physiol. 1992 Dec;263(6 Pt 2):F985-90. doi: 10.1152/ajprenal.1992.263.6.F985.
The inner medullary collecting duct is a complex tissue that exhibits a variety of hormone signaling systems. These include the following: adenylyl cyclase activity stimulated by vasopressin (AVP), beta-adrenergic agonists, or prostanoids and inhibited by alpha 2-adrenergic agents or adenosine; guanylate cyclase activity in response to atrial natriuretic peptide (ANP); phospholipase C activity stimulated by ANP, AVP, bradykinin, endothelin, epidermal growth factor (EGF), and muscarinic cholinergic agents; and phospholipase A2 activity stimulated by AVP, bradykinin, EGF, and endothelin. The signal transduction mechanisms for each of these hormone signaling systems is succinctly reviewed, and the interactions between different signaling pathways are discussed. Central to this interaction is the mutually inhibitory relationship between activation of adenylyl cyclase and phospholipases. Increasing cellular adenosine 3',5'-cyclic monophosphate content impairs activation of phospholipases A2 and C; conversely, stimulation of phospholipase C impairs AVP-stimulated adenylyl cyclase activity via activation of protein kinase C.
内髓集合管是一种复杂的组织,具有多种激素信号系统。这些系统包括:血管加压素(AVP)、β-肾上腺素能激动剂或前列腺素刺激的腺苷酸环化酶活性,以及α2-肾上腺素能药物或腺苷抑制的腺苷酸环化酶活性;心房利钠肽(ANP)刺激的鸟苷酸环化酶活性;ANP、AVP、缓激肽、内皮素、表皮生长因子(EGF)和毒蕈碱胆碱能药物刺激的磷脂酶C活性;以及AVP、缓激肽、EGF和内皮素刺激的磷脂酶A2活性。本文简要综述了这些激素信号系统各自的信号转导机制,并讨论了不同信号通路之间的相互作用。这种相互作用的核心是腺苷酸环化酶激活与磷脂酶之间的相互抑制关系。增加细胞内3',5'-环磷酸腺苷含量会损害磷脂酶A2和C的激活;相反,磷脂酶C的刺激会通过蛋白激酶C的激活损害AVP刺激的腺苷酸环化酶活性。