课题基金 / 基金详情

DESENSITIZATION OF LH SECRETION BY GNRH

DESENSITIZATION OF LH SECRETION BY GNRH
GNRH 对 LH 分泌的脱敏作用
批准号:
2889336
负责人:
JIMMY D NEILL
金额:
$27.16万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-04-10 至 2001-03-31

项目摘要

项目成果

JIMMY D NEILL的其他基金

相似基金

相关文献

中文摘要
翻译
描述(改编自研究者摘要):脱敏
英文摘要
DESCRIPTION (Adapted from the Investigator's Abstract): Desensitization of LH secretion by the gonadotrope is a hallmark of GnRH action unless it is administered or secreted in a pulsatile fashion. The cellular and molecular mechanisms of gonadotrope desensitization is poorly understood. A class of proteins discovered originally in yeast have been described as being involved in mammalian cell desensitization. Called regulators of G-protein signalling (RGS), one of these proteins (RGS-3) has been shown by us to inhibit GnRH-stimulated cellular inositol trisphosphate (IP3) levels, its mRNA is present in the gonadotropic aT3-1 cell line, and RGS is detected by antibodies in membranes of aT3-1 and pituitary cells. RGS3 is shown to bind the Gqa protein in vitro supporting the notion that RGSs act by binding G proteins, thus inhibiting G-protein coupling of the receptor to phospholipase C activation. Fifteen mammalian genes encoding RGSs have been identified. The Specific Aims are to: (1) complete the preliminary characterization of RGS3 as participating in GnRH-induced desensitization; (2) Determine if other members of the 15 member RGS family are involved in GnRH-induced desensitization by screening RNA from GnRH-treated aT3-1 cells; (3) Investigate the role of RGS in GnRH-induced desensitization of LH secretion in purified rat pituitary gonadotropes. The experiments have the potential to provide a cellular and molecular explanation of GnRH-induced desensitization, and perhaps provide an entree to the wider issue of regulation of general gonadotrope responsiveness.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1186/1471-2121-2-21
发表时间: 2001
期刊: BMC cell biology
影响因子: --
作者: [Neill JD, Duck LW, Sellers JC, Musgrove LC, Kehrl JH]
通讯作者: Kehrl JH
Potential regulatory roles for G protein-coupled receptor kinases and beta-arrestins in gonadotropin-releasing hormone receptor signaling.
G 蛋白偶联受体激酶和 β-抑制素在促性腺激素释放激素受体信号传导中的潜在调节作用。
DOI: 10.1210/endo.139.4.5868
发表时间: 1998
期刊: Endocrinology
影响因子: 4.8
作者: [Neill,JD, Duck,LW, Musgrove,LC, Sellers,JC]
通讯作者: Sellers,JC
High efficiency method for gene transfer in normal pituitary gonadotropes: adenoviral-mediated expression of G protein-coupled receptor kinase 2 suppresses luteinizing hormone secretion.
正常垂体促性腺激素基因转移的高效方法:腺病毒介导的 G 蛋白偶联受体激酶 2 表达抑制黄体生成素分泌。
DOI: 10.1210/endo.140.6.6688
发表时间: 1999
期刊: Endocrinology
影响因子: 4.8
作者: [Neill,JD, Musgrove,LC, Duck,LW, Sellers,JC]
通讯作者: Sellers,JC
RESPONSIVENESS OF GNRH RECEPTOR SIGNALING
RESPONSIVENESS OF GNRH RECEPTOR SIGNALING
RESPONSIVENESS OF GNRH RECEPTOR SIGNALING
RESPONSIVENESS OF GNRH RECEPTOR SIGNALING
海外基金