GnRH Signaling Mechanisms in the Pituitary Gonadotrope
GnRH Signaling Mechanisms in the Pituitary Gonadotrope
批准号:
8299112
负责人:
Mark Andrew Lawson
金额:
$31.15万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-03-20 至 2015-06-30
关键词:
AddressAnterior Pituitary GlandApoptosisAreaCell DeathCell Differentiation processCell physiologyCellsCellular StressComplexCuesDietElementsEndoplasmic ReticulumEventFatty acid glycerol estersFeedbackFollicle Stimulating HormoneFrequenciesGene ExpressionGenesGenetic TranscriptionGlycoproteinsGonadotrope CellGonadotropin Hormone Releasing HormoneGonadotropin-Releasing Hormone ReceptorGonadotropinsHomeostasisHormonesHypothalamic structureIn VitroInflammatoryKnock-outKnockout MiceLeadLinkLuteinizing HormoneMediatingMediator of activation proteinMessenger RNAMetabolic stressMonitorMusNeuraxisNormal CellOvulationPhosphotransferasesPhysiologic pulsePhysiologicalPituitary GlandPolyribosomesPost-Transcriptional RegulationPredispositionProductionProtein BiosynthesisProteinsRNA BindingReceptor SignalingRegulationRegulatory PathwayReproductionRibonucleoproteinsRoleSchemeSignal TransductionSpecificityStressStructureSystemTestingTranslation InitiationTranslationsVertebratesactivating transcription factorbasebiological adaptation to stresscell growthendoplasmic reticulum stresshormone sensitivitymeetingsmouse modelnovelpublic health relevancereproductivereproductive functionreproductive hormonereproductive successresponsestress management
中文摘要
描述(由申请人提供):促性腺激素释放激素(GnRH)受体的激活启动了垂体促性腺激素中许多复杂的信号级联反应。促性腺激素的节律性刺激是促黄体生成素和促卵泡激素产生差异控制的基础,并最终控制生殖。GnRH受体信号级联调节促性腺激素分泌、基因转录和细胞分化。我们已经证明GnRH调节蛋白质合成并激活未折叠蛋白反应(UPR),这是一种调节蛋白质合成压力需求的保护性反应。普遍定期审议也被炎症和代谢应激信号激活。GnRH受体利用的调节方案对于维持细胞稳态和对反复出现的GnRH脉冲的敏感性至关重要。为了维持脉冲敏感性和激素合成,促性腺激素必须解决由分泌引起的细胞内改变,增加蛋白质合成以继续满足这些需求,并解决由前一个脉冲激活的信号事件,以便对下一个脉冲做出充分反应。我们已经确定了UPR和翻译控制是维持促性腺激素对GnRH的敏感性和生物合成能力的中心因素。我们建议在体外研究这些成分以确定它们的调节机制,并在实验小鼠模型中确定它们在生殖中的生理作用。普遍定期审议可能提供生理应激和生殖功能之间的直接联系。特异性目的1:未折叠蛋白在促性腺激素功能中的反应。我们将确定未折叠蛋白反应的三个主要调节因子EIF2AK3和ERN1在正常促性腺激素细胞功能中的作用。特异性目的2:GnRH对mRNA再分布的反应机制我们已经证明GnRH会导致促性腺激素中mRNA的再分布。我们将确定再分配的特异性和决定再分配易感性的因素。我们将通过检测垂体特异性敲除关键UPR调节因子对生殖的影响,来研究未折叠蛋白反应在正常促性腺细胞功能中的作用。
英文摘要
DESCRIPTION (provided by applicant): Activation of the gonadotropin-releasing hormone (GnRH) receptor initiates a number of complex signaling cascades in pituitary gonadotropes. The rhythmic stimulation of gonadotropes by pulsatile GnRH underlies the differential control of luteinizing hormone and follicle-stimulating hormone production, and ultimately the control of reproduction. GnRH receptor signaling cascades regulate gonadotropin secretion, gene transcription and cell differentiation. We have shown that GnRH regulates protein synthesis and activates the unfolded protein response (UPR), a protective response to modulate stressful demands of protein synthesis. The UPR also activated by inflammatory and metabolic stress signals. The regulatory schemes utilized by the GnRH receptor are essential to maintain cell homeostasis and sensitivity to recurring GnRH pulses. To maintain pulse sensitivity and hormone synthesis, gonadotropes must resolve the intracellular alterations induced by secretion, increase protein synthesis to continue to meet these demands, and resolve the signaling events activated by the previous pulse to allow full response to the next. We have identified the UPR and control of translation as central elements maintaining gonadotrope sensitivity to GnRH and biosynthetic capacity. We propose to examine these components in vitro to determine their mechanism of regulation and in experimental mouse models to determine their physiological role in reproduction. The UPR may provide a direct link between physiological stress and reproductive function. Specific Aim 1: The Unfolded Protein Response in gonadotrope function. We will determine the role of the three main regulators of the unfolded protein response, EIF2AK3 and ERN1, in normal gonadotrope cell function Specific Aim 2: Mechanisms of mRNA redistribution in response to GnRH We have demonstrated that GnRH causes a redistribution of mRNA in gonadotropes. We will determine the specificity of redistribution and the factors determining susceptibility to redistribution. Specific Aim 3: Physiological consequences of an impaired stress response in mice We will examine the role of the unfolded protein response in normal gonadotrope cell function by examining the reproductive impact of pituitary-specific knockout of critical UPR regulatory factors.
PUBLIC HEALTH RELEVANCE: To preserve normal reproductive hormone production and to respond correctly to environmental cues, pituitary cells must minimize cellular stress and adapt to the demand of continued hormone production. We are investigating the mechanisms cells use to adapt to stress and preserve normal cell function. These regulatory pathways are essential to assure proper reproductive hormone synthesis and reproductive success.
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海外基金