SECOND MESSENGER FUNCTION IN EXOCRINE GLANDS

外分泌腺的第二信使功能

• 批准号: 3220966
• 负责人: THOMAS W HURLEY
• 金额: $ 13.27万
• 依托单位: UNIVERSITY OF MISSOURI-COLUMBIA
• 依托单位国家: 美国
• 财政年份: 1985
• 资助国家: 美国
• 起止时间: 1985-09-01 至 1990-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/3220966
• 关键词: 3'5' cyclic nucleotide phosphodiesterase; adenosine triphosphate; adenosinetriphosphatase; adenylate cyclase; alpha adrenergic agent; amylases; autoradiography; beta adrenergic agent; calcium metabolism; cholinergic agents; cyclic AMP; cyclic GMP; cyclic nucleoside monophosphate; cytoplasm; exocrine glands; gel electrophoresis; guanylate cyclase; hormone regulation /control mechanism; ion transport; membrane permeability; messenger RNA; pancreas; peptidyl dipeptidase A; phosphorylation; potassium; protein kinase; radiotracer; secretion; sialate; submandibular gland

The mechanism of secretion in salivary glands and the pancreas requires Ca2+ and the cyclic nucleotides, but the precise roles of those second messengers and the regulation of their cytosolic concentrations are only partially understood. These studies will evaluate the hypothesis that control of second messenger concentration effected, in part, by the second messengers themselves. This hypothesis will be tested in comparative studies using acinar preparations of the rat submandibular gland and pancreas as model systems to (1) characterize the kinetic and regulatory properties of the enzymes that control second messenger concentration: high affinity CaATPase and active Ca2+ translocation, adenylate and guanylate cyclase activities and cAMP and cGMP phosphodiesterase activities; and (2) characterize the kinetic properties of the forms of those enzymes regulated by the Ca2+-calmodulin complex. A second goal of these studies is to determine the effects of second messengers on kinase activities in exocrine glands and to evaluate the hypothesis that secretion depends on second messenger-regulated protein phosphorylation. Polyacrylamide gel electrophoresis and autoradiography will be used to detect and characterize the phosphorylated substrates of kinases regulated by the second messengers in broken acinar cells. In other studies, functioning acinar preparations will be incubated with P32 to label intracellular ATP then exposed to cholinergic, Alpha and Beta adrenergic or peptidergic agents. Secretory responses (in terms of release of K+, of amylase or as sialic acid liberated from secreted glycoproteins) will be measured at various times thereafter and correlated with changes in protein phosphorylation. In parallel studies, acini will be exposed to secretagogues in the presence of agents which inhibit, augment and/or mimic the effects of the second messengers in order to correlate changes in second messenger-dependent phosphorylation with changes in secretory response. These studies will yield new information concerning the mechanism of stimulus-secretion coupling in well-defined model exocrine systems and will provide new insights regarding the comparative physiology of secretory systems involved in a variety of diseases. In addition these studies will be important in defining the factors that regulate normal salivary gland function and therefore are important for the maintenance of healthy soft and mineralized tissue in the oral cavity.

唾液腺和胰腺分泌的机制需要