Knockout of microglial Hv1 proton channel reduces neurotoxic A1 astrocytes and neuronal damage via the ROS/STAT3 pathway after spinal cord injury

• Published in: Glia 2023-10, Vol.71 (10), p.2418-2436
• Main Authors: Li, Ying, Xie, Yi, Liu, Rui, Wang, Ziyue, Chen, Peng, Wang, Minghuan, Yu, Zhiyuan, Wang, Wei, Luo, Xiang
• Format: Article
• Language: English
• Subjects: A1/A2 astrocytes; Acetylcysteine; Astrocytes; Damage; Genotype & phenotype; Injury prevention; Microglia; Neuronal-glial interactions; Neuroprotection; Neurotoxicity; Phagocytosis; Phenotypes; Protons; Reactive oxygen species; Spinal cord injuries; spinal cord injury; Stat3 protein; Synaptogenesis; voltage‐gated proton channel Hv1
• ISSN: 0894-1491; 1098-1136
• DOI: 10.1002/glia.24433

Spinal cord injury (SCI) causes severe functional deficits and neuronal damage, accompanied by intense glial activation. The voltage‐gated proton channel Hv1, selectively expressed on microglia, is associated with SCI progression. However, the effect of Hv1 on the phenotypes and functions of reactive astrocytes after SCI remains unclear. Here, we combined Hv1 knockout (Hv1−/−) mice and T10 spinal cord contusion to investigate the effects of microglial Hv1 on SCI pathophysiology and the phenotypes and functions of reactive astrocytes. After SCI, astrocytes proliferated and activated in the peri‐injury area and exhibited an A1‐dominant phenotype. Hv1 knockout reduced neurotoxic A1 astrocytes and shifted the dominant phenotype of reactive astrocytes from A1 to A2, enhancing synaptogenesis promotion, phagocytosis, and neurotrophy of astrocytes. Moreover, synaptic and axonal remodeling as well as motor recovery after SCI benefited from the improved astrocytic functions of Hv1 knockout. Furthermore, exogenous and endogenous reactive oxygen species (ROS) in astrocytes after SCI were reduced by Hv1 knockout. Our in vitro results showed that inhibition of ROS reduced the neurotoxic A1 phenotype in primary astrocytes via the STAT3 pathway. Similar to the effect of Hv1 knockout, the application of the ROS scavenger N‐acetylcysteine reduced SCI‐induced neurotoxic A1 astrocytes in vivo. Based on the in vivo and vitro results, we elucidated that microglial Hv1 knockout promotes synaptic and axonal remodeling in SCI mice by decreasing neurotoxic A1 astrocytes and increasing neuroprotective A2 astrocytes via the ROS/STAT3 pathway. Therefore, the Hv1 proton channel is a promising target for the treatment of SCI. Main Points SCI increases neurotoxic A1‐like astrocytes. Hv1 knockout reduces ROS production and shifts the dominant phenotype from A1 to A2 after SCI. ROS levels affect the astrocyte phenotypes and functions via the STAT3 pathway in vitro.