Isoform-specific inhibition of calcineurin to prevent nephrotoxicity

钙调神经磷酸酶异构体特异性抑制可预防肾毒性

• 批准号: 7082384
• 负责人: JENNIFER L GOOCH
• 金额: $ 22.95万
• 依托单位: EMORY UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-04-01 至 2008-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7082384
• 关键词: artificial immunosuppression; calcineurin; cardiotoxin; drug adverse effect; enzyme inhibitors; gene targeting; genetic models; genetically modified animals; hyperlipidemia; immunosuppressive; isozymes; laboratory mouse; model design /development; renal toxin; skin transplantation; toxicology

DESCRIPTION (provided by applicant): L-Calcineurin is an important regulatory enzyme that functions in many cellular processes including T cell signal transduction. Drug such as cyclosporin and FK506 that inhibit calcineurin (CIs) are clinically useful to suppress the immune system following organ transplantation. Unfortunately, inhibition of calcineurin also affects tissues other than the immune system and long-term use of CIs often produces therapeutically-limiting side-effects including nephrotoxicity and cardiovascular disease. Work in our laboratory is focused on specificity of calcineurin action in the kidney. Interestingly, when we examined mice that lack the alpha isoform of the catalytic subunit of calcineurin and mice that lack the beta isoform, we find very different effects. Namely, loss off alpha severely impairs development of the kidney, alters cell cycle regulation, and results in increased matrix production - features consistent with Cl nephrotoxicity while mice lacking the beta isoform lack signs of significant renal damage. Moreover, we find that alpha-/- mice develop hyperlipidemia, demonstrating a direct connection between calcineurin action and development of cardiovascular disease. Finally, mice lacking the beta isoform have been previously described to have an "immune-suppressed"-like phenotype while T cell function in alpha null animals can still be suppressed with cyclosporin. These mouse models clearly demonstrate that calcineurin isoforms have distinct functions that are particularly relevant in the transplant setting. Inhibition of the alpha isoform produces nephrotoxicity and hyperlipidemia while inhibition of the beta isoform results in suppression of T cell signaling. Therefore, we hypothesize that selective inhibition of the beta isoform will result in immune suppression with fewer toxic side-effects. To test this hypothesis, it will be necessary to generate a mouse model that will allow us to carefully compare the effects of selective loss of calcineurin isoforms. Since alpha-/- mice live only a few weeks, it is not currently possible to perform such studies. However, recent advances in gene manipulations provide innovative tools to generate inducible, isoform-specific knockout mice. We will create these mice and characterize the effect of inducible loss of each isoform in immune suppression and nephrotoxic / cardio- vascular side- effects. Using a well-characterized skin transplant model, we will then test the hypothesis that selective inhibition of calcineurin isoforms results in immune suppression with fewer side-effects.

描述（申请人提供）：l -钙调磷酸酶是一种重要的调节酶，在包括T细胞信号转导在内的许多细胞过程中起作用。环孢素和FK506等抑制钙调磷酸酶（CIs）的药物在临床上可用于器官移植后的免疫系统抑制。不幸的是，钙调磷酸酶的抑制也会影响免疫系统以外的组织，长期使用CIs通常会产生治疗限制性副作用，包括肾毒性和心血管疾病。我们实验室的工作重点是研究钙调磷酸酶在肾脏中的特异性作用。有趣的是，当我们检查缺乏钙调磷酸酶催化亚基α亚型的小鼠和缺乏β亚型的小鼠时，我们发现了非常不同的影响。也就是说，α的缺失会严重损害肾脏的发育，改变细胞周期调节，并导致基质生成增加——这与Cl肾毒性一致，而缺乏β亚型的小鼠则没有明显的肾损伤迹象。此外，我们发现α -/-小鼠发生高脂血症，证明钙调磷酸酶作用与心血管疾病的发展之间存在直接联系。最后，缺乏β亚型的小鼠先前被描述为具有“免疫抑制”样表型，而α缺失动物的T细胞功能仍然可以被环孢素抑制。这些小鼠模型清楚地表明，钙调磷酸酶同种异构体具有与移植环境特别相关的独特功能。α -异构体的抑制产生肾毒性和高脂血症，而β -异构体的抑制导致T细胞信号传导的抑制。因此，我们假设选择性抑制β异构体将导致免疫抑制，毒副作用更少。为了验证这一假设，有必要建立一个小鼠模型，使我们能够仔细比较选择性丧失钙调磷酸酶同种异构体的影响。由于α -/-小鼠只能存活几周，目前还不可能进行这样的研究。然而，最近在基因操作方面的进展提供了创新的工具来产生可诱导的、异构体特异性敲除小鼠。我们将创建这些小鼠，并描述诱导丢失每种异构体在免疫抑制和肾毒性/心血管副作用中的作用。使用一个特征良好的皮肤移植模型，我们将验证选择性抑制钙调神经磷酸酶异构体导致免疫抑制且副作用更少的假设。