肿瘤坏死因子α介导的小胶质细胞与米勒细胞之间的相互作用加剧实验性青光眼中的视网膜神经节细胞损伤
Tumor Necrosis Factor Alpha-Mediated Interaction Between Microglia and Müller Cells Exacerbates Retinal Ganglion Cell Damage in Experimental Glaucoma.
作者信息
Li Shu-Ying, Zhou Hong, Zhao Guoli, Ding Wen-Wen, Zhang Yu, Wang Yong-Chen, Li Fang, Miao Yanying, Sun Xing-Huai, Wang Zhongfeng
机构信息
State Key Laboratory of Brain Function and Disorders and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, Shanghai, 200032, China.
Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, NHC Key Laboratory of Myopia, Shanghai Key Laboratory of Visual Impairment and Restoration, Fudan University, Shanghai, 200031, China.
出版信息
Neurosci Bull. 2025 Aug 30. doi: 10.1007/s12264-025-01478-1.
Interaction between Müller cells and microglia aggravates neuroinflammation, resulting in retinal ganglion cell (RGC) death in glaucoma. Here, we investigated how tumor necrosis factor-alpha (TNF-α) produced by activated microglia mediates the crosstalk between Müller cells and microglia and impacts RGC injury in a chronic ocular hypertension (COH) glaucoma model. In COH retinas, elevated TNF-α induced the activation of Müller cells and microglia, and recruited microglia to the ganglion cell layer. Co-culture with Müller cells enhanced TNF-α-induced microglial activation, migration, and proliferation. Both in vivo and in vitro experiments confirmed that chemokine C-C motif ligand 2 (CCL2), primarily released from Müller cells, mediated the TNF-α-induced effects on microglia in COH retinas. Knockdown of CCL2 attenuated RGC damage and vision loss. Our results demonstrate that TNF-α released from microglia induces the secretion of CCL2 from Müller cells, thus inducing microglial activation and migration, exacerbating retinal neuroinflammation and RGC injury in glaucoma.
米勒细胞与小胶质细胞之间的相互作用会加剧神经炎症,导致青光眼患者视网膜神经节细胞(RGC)死亡。在此,我们研究了活化的小胶质细胞产生的肿瘤坏死因子-α(TNF-α)如何介导米勒细胞与小胶质细胞之间的串扰,并在慢性高眼压(COH)青光眼模型中影响RGC损伤。在COH视网膜中,升高的TNF-α诱导米勒细胞和小胶质细胞活化,并将小胶质细胞募集至神经节细胞层。与米勒细胞共培养可增强TNF-α诱导的小胶质细胞活化、迁移和增殖。体内和体外实验均证实,主要由米勒细胞释放的趋化因子C-C基序配体2(CCL2)介导了TNF-α对COH视网膜中小胶质细胞的诱导作用。敲低CCL2可减轻RGC损伤和视力丧失。我们的结果表明,小胶质细胞释放的TNF-α诱导米勒细胞分泌CCL2,从而诱导小胶质细胞活化和迁移,加剧青光眼患者的视网膜神经炎症和RGC损伤。