Membrane and intracellular progesterone receptors as determinants of the

膜和细胞内孕酮受体作为决定因素

• 批准号: 8974805
• 负责人: Meharvan Singh
• 金额: $ 24.96万
• 依托单位: UNIVERSITY OF NORTH TEXAS HLTH SCI CTR
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-08-15 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/8974805
• 关键词: Address; Affect; Age; Animal Model; Brain; Brain-Derived Neurotrophic Factor; Cell Line; Cell model; Cells; Characteristics; Clinical; Complement; Coupled; Cytoprotection; Data; Estradiol; Estrogens; Funding; Future; Goals; Hippocampus (Brain); Human; Injury; Instruction; Intracellular Membranes; Knowledge; Literature; MAP Kinase Gene; MAPK3 gene; MAPK7 gene; Mediating; Mediator of activation protein; Membrane; Menopause; Metabolic; Middle Cerebral Artery Occlusion; Modeling; Molecular; Motor; Neurobiology; Neuroglia; Neurons; Operative Surgical Procedures; Ovariectomy; Pathway interactions; Pattern; Physiological; Primary Cell Cultures; Progesterone; Progesterone Receptors; Refractory; Regulation; Research; Role; Signal Pathway; Steroids; Stroke; Testing; Therapeutic; Time; Translating; Woman; aged; base; brain dysfunction; brain tissue; cognitive function; deprivation; hormone therapy; in vivo; insight; neuroprotection; novel; predicting response; programs; protective effect; receptor; receptor expression; research study; response; steroid hormone; tool

PROJECT SUMMARY (See instructions): During the first period of funding. Project 1 focused on addressing the role of progesterone receptors in mediating the cytoprotective effects of progesterone (P4). In particular. Project 1 challenged the dogma that classical progesterone receptors (PR) are the principal mediators of P4's protective effects in the brain by suggesting that recently described membrane-associated progesterone receptors may be equally important. Major findings included the observation that indeed both the classical PR and membrane-associated progesterone receptors, particularly Pgrmcl, cooperate to regulate key cytoprotective mediators, including effectors of the ERK/MAPK pathway (such as ERK1/2 and ERK5) and BDNF. In the continuation of this project, we propose to apply this knowledge to understand whether 1) there is a finite period (i.e., therapeutic window) following steroid hormone deprivation, or with age, where P4's effects on neuroprotection and key mediators of cytoprotection are maintained, and 2) if the relative abundance of PR and Pgrmcl predict sustained protective effects of P4. Further, we will determine whether specific patterns of progesterone receptor expression predict whether P4 complements or antagonizes estrogen's protective effects. Our hypothesis states that the combined expression of the classical PR and the membrane progesterone receptor, Pgrmcl, is required to maintain responsiveness of the brain to P4. Further, we propose that the relative abundance of these two receptors will also predict whether P4 complements estrogen's protective program or whether it antagonizes estrogen's effects. These hypotheses will be tested in cellular models, where the relative levels of PR and Pgrmcl can be manipulated (pharmacologically or using molecular tools), as well as in an animal model of steroid deprivation (ovariectomy), and finally, translated to a human model of ovariectomy (i.e., the surgical menopause). While the loss of estrogen's beneficial effects with increasing post-ovariectomy duration has been described, nothing is known with respect to the response to P4. Thus, the studies proposed herein will reveal a key piece of the "therapeutic window" puzzle by defining which progesterone receptors are critical determinants of P4's protective effects and importantly, may offer unique insight into how the therapeutic window may be expanded (i.e., through regulation of specific progesterone receptors). Together with the studies proposed in Projects 2 and 3, we expect this program of research to advance our understanding of the neurobiological basis of the "critical window" of therapeutic opportunity for estrogen and progesterone, a goal that could not be achieved by Project 1 alone.

项目概要（见说明）：在第一个供资期间。项目1集中于解决孕酮受体在介导孕酮（P4）的细胞保护作用中的作用。尤其是。项目1挑战了经典孕酮受体（PR）是P4在脑中保护作用的主要介质的教条，提出最近描述的膜相关孕酮受体可能同样重要。主要的发现包括观察到经典的PR和膜相关的孕酮受体，特别是Pgrmcl，确实合作调节关键的细胞保护介质，包括ERK/MAPK途径的效应子（如ERK 1/2和ERK 5）和BDNF。在这个项目的延续中，我们建议应用这些知识来理解1）是否有一个有限的时期（即，治疗窗），其中P4对神经保护和细胞保护的关键介质的作用得以维持，以及2）PR和Pgrmcl的相对丰度是否预测P4的持续保护作用。此外，我们将确定是否孕激素受体表达的特定模式预测是否P4补充或拮抗雌激素的保护作用。我们的假设指出，经典PR和膜孕酮受体Pgrmcl的组合表达是维持大脑对P4的反应所必需的。此外，我们建议这两种受体的相对丰度也将预测P4是否补充雌激素的保护程序或是否拮抗雌激素的作用。这些假设将在细胞模型中进行测试，其中PR和Pgrmcl的相对水平可以被操纵（直接或使用分子工具），以及在类固醇剥夺（卵巢切除术）的动物模型中进行测试，最后，转化为卵巢切除术的人类模型（即，手术绝经期）。虽然已经描述了随着卵巢切除术后持续时间的增加雌激素的有益作用的丧失，但关于对P4的反应还不清楚。因此，本文提出的研究将通过定义哪些孕酮受体是P4保护作用的关键决定因素来揭示“治疗窗”难题的关键部分，并且重要的是，可以提供对如何扩展治疗窗的独特见解（即，通过调节特定的孕酮受体）。与项目2和3中提出的研究一起，我们希望这项研究计划能够促进我们对雌激素和孕激素治疗机会的“关键窗口”的神经生物学基础的理解，这是项目1无法单独实现的目标。