Department of Anatomy, Shandong University School of Basic Medical Sciences, Jinan, 250012, China; Department of Spine Surgery, Shenzhen People's Hospital, The Second Clinical Medical College, Jinan University, The First Affiliated Hospital, Southern University of Science and Technology, Shenzhen, 518020, China.
Department of Anatomy, Shandong University School of Basic Medical Sciences, Jinan, 250012, China.
Neurosci Res. 2021 Aug;169:9-16. doi: 10.1016/j.neures.2020.06.004. Epub 2020 Jun 25.
The pathogenesis of diabetic peripheral neuropathy (DPN) is complex and not well understood. Recently, oxidative stress and endoplasmic reticulum (ER) stress induced by hyperglycemia have been demonstrated to play a critical role in neuronal apoptosis, which then contributing to DPN. However, the specific molecular mechanism that underlies the hyperglycemia-induced neuronal stresses and apoptosis remains largely unknown. In this study, we demonstrated for the first time that Pim1 kinase is a positive modulator of dorsal root ganglion (DRG) neuron survival in vitro. Hyperglycemia causes compensatory upregulation of Pim1 kinase in the DRG neurons, which provides protection against high glucose-induced oxidative stress and ER stress. Pharmacological inhibition of Pim1 not only sensitizes the stress response to high glucose in the DRG neurons, but also accelerates the apoptosis of DRG neurons in vitro. Therefore, our work provides experimental evidence for the prevention of high glucose-induced neuronal stress and apoptosis by targeting Pim1 kinase.
糖尿病周围神经病变(DPN)的发病机制复杂,目前尚不完全清楚。最近的研究表明,高血糖诱导的氧化应激和内质网(ER)应激在神经元凋亡中起关键作用,进而导致 DPN。然而,高血糖诱导的神经元应激和凋亡的具体分子机制在很大程度上仍不清楚。在这项研究中,我们首次证明 Pim1 激酶是体外背根神经节(DRG)神经元存活的正调节剂。高血糖导致 DRG 神经元中 Pim1 激酶的代偿性上调,为高葡萄糖诱导的氧化应激和 ER 应激提供了保护。Pim1 的药理学抑制不仅使 DRG 神经元对高葡萄糖的应激反应敏感化,而且加速了 DRG 神经元的体外凋亡。因此,我们的工作为通过靶向 Pim1 激酶预防高葡萄糖诱导的神经元应激和凋亡提供了实验依据。