Structure & Function of Epididymis and Vas Deferens

结构

• 批准号: 7019172
• 负责人: KENNETH P ROBERTS
• 金额: $ 26.1万
• 依托单位: UNIVERSITY OF MINNESOTA
• 依托单位国家: 美国
• 财政年份: 1978
• 资助国家: 美国
• 起止时间: 1978-09-29 至 2008-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7019172
• 关键词: SDS polyacrylamide gel electrophoresis; acrosome; active sites; biological signal transduction; calcium channel; calcium flux; confocal scanning microscopy; cysteine; egg /ovum; epididymis; fertilization; glycoproteins; immunoprecipitation; laboratory rat; membrane fusion; membrane proteins; phosphorylation; polymerase chain reaction; protein binding; protein structure; protein structure function; receptor; sperm; sperm capacitation; western blottings

DESCRIPTION (provided by applicant): Funds are requested to study the specific functions of the Crisp-1 protein. Crisp-1 is produced in the epididymis and associates with the sperm during transit through the organ. The high similarity to a known ryanodine receptor agonist suggests that Crisp-1 may have a role in ion channel regulation. Changes in calcium concentrations are required for sperm to become capacitated and undergo the acrosome reaction in preparation for fertilization. In vitro capacitation studies of rat sperm show that when Crisp-1 is present, sperm are prohibited from capacitating. The specific aims focus on determining the mechanisms involved in the inhibition of capacitation by Crisp-l, identification of the receptor for Crisp-1 on sperm, identification of the Crisp-1 active site, and investigation of the ability of other members of the Crisp family to mimic the actions of Crisp-1. Crisp-1 will also be tested for its ability to inhibit capacitation and the acrosome reaction in human sperm. Finally, potential actions of Crisp-1 on the egg, such as the ability to regulate cortical granule fusion, will be examined. The proposed studies will provide significant contributions to our understanding of sperm function and may also have potential application to male infertility and contraceptive development.

描述（由申请人提供）：申请资金用于研究Crisp-1蛋白的特定功能。Crisp-1在附睾中产生，并在精子通过该器官的过程中与精子结合。Crisp-1与一种已知的ryanodine受体激动剂高度相似，这表明Crisp-1可能在离子通道调节中起作用。钙浓度的变化是精子获得能力和进行顶体反应为受精做准备所必需的。对大鼠精子的体外获能研究表明，当Crisp-1存在时，精子被禁止获能。具体目的是确定Crisp-1抑制获能的机制，鉴定Crisp-1在精子上的受体，鉴定Crisp-1的活性位点，以及研究Crisp家族其他成员模仿Crisp-1作用的能力。Crisp-1还将测试其抑制人类精子获能和顶体反应的能力。最后，将研究Crisp-1对卵子的潜在作用，如调节皮质颗粒融合的能力。该研究将为我们对精子功能的理解做出重大贡献，并可能在男性不育和避孕药开发方面具有潜在的应用价值。