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Structure & Function of Epididymis and Vas Deferens

Structure & Function of Epididymis and Vas Deferens
结构
批准号:
7210587
负责人:
KENNETH P ROBERTS
金额:
$25.34万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1978
资助国家:
美国
项目状态:
已结题
起止时间:
1978-09-29 至 2008-03-31

项目摘要

项目成果

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中文摘要
翻译
描述(申请人提供):请求资金研究Crisp-1蛋白的具体功能。Crisp-1在附睾中产生,并在通过该器官的过程中与精子结合。与已知的ryanodine受体激动剂的高度相似性表明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准备受精所必需的。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。具体目标集中于确定Crisp-1抑制获能的机制,鉴定精子上Crisp-1的受体,鉴定Crisp-1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,将检查Crisp-1对卵的潜在作用,例如调节皮质颗粒融合的能力。这些研究将为我们理解精子功能做出重大贡献,也可能对男性不育和避孕开发具有潜在的应用价值。
英文摘要
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.
期刊论文(29)
专著(0)
科研奖励(0)
会议论文
Dolichol concentration and biosynthesis in rat testis and epididymis.
大鼠睾丸和附睾中的多醇浓度和生物合成。
DOI: 10.1095/biolreprod23.5.1054
发表时间: 1980
期刊: Biology of reproduction
影响因子: 3.6
作者: [Wenstrom,JC, Hamilton,DW]
通讯作者: Hamilton,DW
Immunocytochemical evidence for the specific localization of aldose reductase in rat Sertoli cells.
大鼠支持细胞中醛糖还原酶特异性定位的免疫细胞化学证据。
DOI: 10.1095/biolreprod26.2.311
发表时间: 1982
期刊: Biology of reproduction
影响因子: 3.6
作者: [Ludvigson,MA, Waites,GM, Hamilton,DW]
通讯作者: Hamilton,DW
An 18-kDa androgen-regulated protein that modifies galactosyltransferase activity is synthesized by the rat caput epididymidis, but has no structural similarity to rat milk alphalactalbumin.
一种可修饰半乳糖基转移酶活性的 18 kDa 雄激素调节蛋白由大鼠附睾合成,但与大鼠乳汁 α-乳白蛋白没有结构相似性。
DOI: 10.1095/biolreprod43.3.497
发表时间: 1990
期刊: Biology of reproduction
影响因子: 3.6
作者: [Moore,A, Hall,L, Hamilton,DW]
通讯作者: Hamilton,DW
Membrane glycoproteins from spermatozoa: partial characterization of an integral Mr = approximately 24,000 molecule from rat spermatozoa that is glycosylated during epididymal maturation.
来自精子的膜糖蛋白:来自大鼠精子的完整 Mr = 大约 24,000 个分子的部分表征,该分子在附睾成熟过程中被糖基化。
DOI: 10.1095/biolreprod34.5.925
发表时间: 1986
期刊: Biology of reproduction
影响因子: 3.6
作者: [Hamilton,DW, Wenstrom,JC, Baker,JB]
通讯作者: Baker,JB
22
    New Approaches to Rat Sperm Cryopreservation
    • 批准号:
      6906674
    • 项目类别:
    • 资助金额:
      $20.45万
    • 财政年份:
      2005
    • 负责人:
      KENNETH P ROBERTS
    • 依托单位:
    HORMONAL REGULATION OF SERTOLI CELL FUNCTION
    • 批准号:
      3049150
    • 项目类别:
    • 资助金额:
      $2.86万
    • 财政年份:
      1992
    • 负责人:
      KENNETH P ROBERTS
    • 依托单位:
    HORMONAL REGULATION OF SERTOLI CELL FUNCTION
    • 批准号:
      3049149
    • 项目类别:
    • 资助金额:
      $2.27万
    • 财政年份:
      1991
    • 负责人:
      KENNETH P ROBERTS
    • 依托单位:
    FACULTY DEVELOPMENT IN GIM AND/OR GP
    • 批准号:
      3015730
    • 项目类别:
    • 资助金额:
      $0.0万
    • 财政年份:
      1987
    • 负责人:
      KENNETH P ROBERTS
    • 依托单位:
    国内基金
    海外基金
    原生动物四膜虫生殖小核(germline nucleus)体功能(somatic function)的分子基础研究