Gebru Niat T, Hill Shannon E, Blair Laura J
USF Health Byrd Alzheimer's Institute, University of South Florida, Tampa, Florida, USA.
Department of Molecular Medicine, University of South Florida, Tampa, Florida, USA.
J Cell Biochem. 2024 Dec;125(12):e30374. doi: 10.1002/jcb.30374. Epub 2023 Feb 13.
FK506 binding protein 51 (FKBP51) is a molecular chaperone that influences stress response. In addition to having an integral role in the regulation of steroid hormone receptors, including glucocorticoid receptor, FKBP51 has been linked with several biological processes including metabolism and neuronal health. Genetic and epigenetic alterations in the gene that encodes FKBP51, FKBP5, are associated with increased susceptibility to multiple neuropsychiatric disorders, which has fueled much of the research on this protein. Because of the complexity of these processes, animal models have been important in understanding the role of FKBP51. This review examines each of the current mouse models of FKBP5, which include whole animal knockout, conditional knockout, overexpression, and humanized mouse models. The generation of each model and observational details are discussed, including behavioral phenotypes, molecular changes, and electrophysiological alterations basally and following various challenges. While much has been learned through these models, there are still many aspects of FKBP51 biology that remain opaque and future studies are needed to help illuminate these current gaps in knowledge. Overall, FKBP5 continues to be an exciting potential target for stress-related disorders.
FK506结合蛋白51(FKBP51)是一种影响应激反应的分子伴侣。除了在包括糖皮质激素受体在内的类固醇激素受体调节中发挥不可或缺的作用外,FKBP51还与包括代谢和神经元健康在内的多种生物学过程相关。编码FKBP51的基因FKBP5中的遗传和表观遗传改变与多种神经精神疾病的易感性增加有关,这推动了对该蛋白的大量研究。由于这些过程的复杂性,动物模型对于理解FKBP51的作用至关重要。这篇综述考察了目前FKBP5的每种小鼠模型,包括全动物敲除、条件性敲除、过表达和人源化小鼠模型。讨论了每种模型的构建及观察细节,包括基础状态下以及在各种刺激后的行为表型、分子变化和电生理改变。虽然通过这些模型已经了解了很多,但FKBP51生物学的许多方面仍然不明确,需要未来的研究来填补当前这些知识空白。总体而言,FKBP5仍然是应激相关疾病一个令人兴奋的潜在靶点。