The Fourth Ward, Department of Neurology, The Third Affiliated Hospital of Qiqihar Medical University, Qiqihar 161000, P.R. China.
Department of Health Care, The Third Affiliated Hospital of Qiqihar Medical University, Qiqihar 161000, P.R. China.
Aging (Albany NY). 2020 Mar 12;12(5):4067-4081. doi: 10.18632/aging.102636.
Parkinson's disease (PD) is a progressive neurodegenerative disorder. A common and disabling disease of the elderly, the standard dopamine replacement therapies do not arrest the ongoing neurodegeneration, thus calling for new treatment strategies. The present study aimed to clarify the functional relevance of the hypoxia inducible factor-1α (HIF-1α)/microRNA-128-3p (miR-128-3p) axis in hippocampal neurodegeneration in a PD mouse model obtained by intraperitoneal injection of MPTP. Targeting relationship between miR-128-3p and was verified, so we probed the roles of , miR-128-3p, and in apoptosis of hippocampal neurons with gain- and loss-of function experiments using flow cytometry and TUNEL staining. We found that was upregulated in hippocampal tissues and cells of the MPTP-lesioned mouse model of PD, while and miR-128-3p were downregulated. Elevation of HIF-1α/miR-128-3p inhibited apoptosis of hippocampal neurons via Wnt/β-catenin signaling pathway activation due to the suppression of in PD. In addition, forced overexpression of could ameliorate motor dysfunction and pathological changes in the model. Collectively, activation of the HIF-1α/miR-128-3p axis could repress hippocampal neurodegeneration in MPTP-lesioned mice through an activated Wnt/β-catenin pathway due to downregulation.
帕金森病(PD)是一种进行性神经退行性疾病。作为一种常见且致残的老年疾病,标准的多巴胺替代疗法并不能阻止持续的神经退行性变,因此需要新的治疗策略。本研究旨在阐明缺氧诱导因子-1α(HIF-1α)/微小 RNA-128-3p(miR-128-3p)轴在 MPTP 腹腔注射诱导的 PD 小鼠模型海马神经退行性变中的功能相关性。验证了 miR-128-3p 与 之间的靶向关系,因此我们通过流式细胞术和 TUNEL 染色的增益和失活功能实验,探讨了 、miR-128-3p 和 在海马神经元凋亡中的作用。我们发现,在 PD 模型的海马组织和细胞中,上调,而下调 miR-128-3p 和 。由于抑制 PD 中的 ,HIF-1α/miR-128-3p 的升高抑制了海马神经元的凋亡,通过激活 Wnt/β-catenin 信号通路。此外, 过表达的强制过表达可以改善模型中的运动功能障碍和病理变化。总之,由于 下调,HIF-1α/miR-128-3p 轴的激活可以通过激活 Wnt/β-catenin 通路来抑制 MPTP 损伤小鼠的海马神经退行性变。