Qiu Meiqian, Zhang Wenhao, Dai Jiahua, Sun Weiwen, Lai Meijing, Tang Shiyi, Xu En, Ning Yuping, Zhan Lixuan
Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
The Affiliated Brain Hospital of Guangzhou Medical University, Guangzhou, China.
Cell Death Dis. 2024 Dec 18;15(12):904. doi: 10.1038/s41419-024-07293-2.
Neuronal necroptosis appears to be suppressed by the deubiquitinating enzyme A20 and is capable to regulate the polarization of microglia/macrophages after cerebral ischemia. We have demonstrated that hypoxic preconditioning (HPC) can alleviate receptor interacting protein 3 (RIP3)-induced necroptosis in CA1 after transient global cerebral ischemia (tGCI). However, it is still unclear whether HPC serves to regulate the phenotypic polarization of microglia/macrophages after cerebral ischemia by mitigating neuronal necroptosis. We hence aim to elucidate the underlying mechanism(s) by which the ubiquitination of RIP3-dependent necroptosis regulated by A20 affects microglia/macrophages phenotype after cerebral ischemic tolerance. We found that microglia/macrophages in CA1 of rats underwent M1 and M2 phenotypic polarization in response to tGCI. Notably, the treatment with HPC, as well as inhibitors of necroptosis, including Nec-1 and mixed lineage kinase domain-like (MLKL) siRNA, attenuated neuroinflammation associated with M1 polarization of microglia/macrophages induced by tGCI. Mechanistically, HPC was revealed to upregulate A20 and in turn enhance the interaction between A20 and RIP3, thereby reducing K63-linked polyubiquitination of RIP3 in CA1 after tGCI. Consequently, RIP3-dependent necroptosis and the M1 polarization of microglia/macrophages were blocked either by HPC or via overexpression of A20 in neurons, which ultimately mitigated cerebral injury in CA1 after tGCI. These data support that A20 serves as a crucial mediator of microglia/macrophages polarization by suppressing neuronal necroptosis in a RIP3 ubiquitination-dependent manner after tGCI. Also, a novel mechanism by which HPC functions in cerebral ischemic tolerance is elucidated.
神经元坏死性凋亡似乎受到去泛素化酶A20的抑制,并且能够在脑缺血后调节小胶质细胞/巨噬细胞的极化。我们已经证明,缺氧预处理(HPC)可以减轻短暂性全脑缺血(tGCI)后CA1区中受体相互作用蛋白3(RIP3)诱导的坏死性凋亡。然而,HPC是否通过减轻神经元坏死性凋亡来调节脑缺血后小胶质细胞/巨噬细胞的表型极化仍不清楚。因此,我们旨在阐明A20调节的RIP3依赖性坏死性凋亡的泛素化影响脑缺血耐受后小胶质细胞/巨噬细胞表型的潜在机制。我们发现,大鼠CA1区的小胶质细胞/巨噬细胞在tGCI刺激下发生M1和M2表型极化。值得注意的是,HPC处理以及坏死性凋亡抑制剂,包括Nec-1和混合谱系激酶结构域样(MLKL)siRNA,减轻了与tGCI诱导的小胶质细胞/巨噬细胞M1极化相关的神经炎症。从机制上讲,HPC被发现上调A20,进而增强A20与RIP3之间的相互作用,从而减少tGCI后CA1区RIP3的K63连接的多聚泛素化。因此,HPC或通过在神经元中过表达A20均可阻断RIP3依赖性坏死性凋亡和小胶质细胞/巨噬细胞的M1极化,最终减轻tGCI后CA1区的脑损伤。这些数据支持,A20通过在tGCI后以RIP3泛素化依赖性方式抑制神经元坏死性凋亡,从而作为小胶质细胞/巨噬细胞极化的关键介质。此外,还阐明了HPC在脑缺血耐受中发挥作用的新机制。