Role of FKBP12/12.6 in Endothelial Function

描述（由申请人提供）：免疫抑制药物可降低移植后器官排斥反应的发生率，但这些药物可导致内皮功能障碍和高血压。我们的长期目标是阐明免疫抑制药物雷帕霉素和FK 506降低一氧化氮（NO）和升高血压的机制，以便将来可以开发不促进高血压和心血管疾病的药物。我们假设这些作用是由于从细胞内钙释放通道中去除FKBP 12/12.6导致基础内皮细胞钙水平增加和内皮NO合酶（eNOS）磷酸化。为了验证这一假设，我们将：1）确定FKBP 12/12.6耗竭对细胞内钙稳态的影响，2）确定FKBP 12/12.6改变后cPKC在eNOS磷酸化、NO产生和血压升高中的作用，3）评估FKBP 12/12.6在内皮功能和血压调节中的作用。我们将使用FKBP 12/12.6的药理学和/或遗传学扰动的组合，并测量对血压、内皮依赖性舒张、NO产生以及eNOS和PKC表达和磷酸化的影响。我们还将测量内皮细胞中FKBP 12/12.6耗竭如何改变细胞内钙稳态，包括细胞内钙动员的幅度、持续时间和位置的变化。抑制免疫系统的药物在器官移植后非常重要，但这些药物可能导致高血压。我们的研究将使用各种基因改变的小鼠和技术来了解这种情况如何发生的机制，希望开发出未来不会产生负面心血管副作用的免疫抑制药物。

DESCRIPTION (provided by applicant): Immunosuppressive drugs reduce the incidence of organ rejection following transplantation, however these drugs can cause endothelial dysfunction and hypertension. Our long-term goal is to elucidate the mechanisms by which the immunosuppressive drugs rapamycin and FK506 decrease nitric oxide (NO) and increase blood pressure so that future drugs can be developed that do not promote hypertension and cardiovascular disease. We hypothesize that these effects arise from removal of FKBP12/12.6 from intracellular calcium release channels resulting in increased basal endothelial cell calcium levels and phosphorylation of endothelial NO synthase (eNOS). To test this hypothesis we will: 1) Determine the effects of FKBP12/12.6 depletion on intracellular calcium homeostasis, 2) Determine the role of cPKC in eNOS phosphorylation, NO production, and blood pressure elevation following alterations of FKBP12/12.6, and 3) Assess the role of FKBP12/12.6 in endothelial function and blood pressure regulation. We will use a combination of pharmacologic and/or genetic perturbations of FKBP12/12.6 and measure the effects on blood pressure, endothelium-dependent dilation, NO production, and eNOS and PKC expression and phosphorylation. We will also measure how FKBP12/12.6 depletion in endothelial cells alters intracellular calcium homeostasis including changes in the magnitude, duration, and location of intracellular calcium mobilization. Drugs that suppress the immune system are extremely important following organ transplantation, however these drugs can cause high blood pressure. Our research will use various genetically altered mice and techniques to understand the mechanisms of how this happens in hopes of developing future immunosuppressive drugs that will not have negative cardiovascular side effects.