Diemler Cory A, MacLean Michael, Heuer Sarah E, Hewes Amanda A, Marola Olivia J, Libby Richard T, Howell Gareth R
The Jackson Laboratory, Bar Harbor, ME, United States.
Graduate School of Biological Sciences and Engineering, University of Maine, Orono, ME, United States.
Front Aging Neurosci. 2024 Jul 2;16:1396443. doi: 10.3389/fnagi.2024.1396443. eCollection 2024.
In recent years, microglia have been highlighted for playing integral roles in neurodegenerative diseases, like glaucoma. To better understand the role of microglia during chronic ocular hypertension, we depleted microglia from aged (9-12 months old) DBA/2 J (D2) mice, which exhibit age-related increases in intraocular pressure, using a dietary CSF1R antagonist, PLX5622. Retinal ganglion cell (RGC) somas were counted, and optic nerve cross-sections stained and assessed for glaucomatous damage. Sustained administration of dietary PLX5622 significantly reduced the numbers of retinal microglia. Dietary PLX5622 did not lead to changes in intraocular pressure in D2 or normotensive DBA/2 J- (D2- ) control mice. While PLX5622-treated D2- did not develop optic nerve damage, PLX5622-treated D2 mice showed a significant increase in moderate-to-severe optic nerve damage compared to D2 mice fed a control diet. In conclusion, global reduction of microglia exacerbated glaucomatous neurodegeneration in D2 mice suggesting microglia play an overall beneficial role in protecting from ocular hypertension associated RGC loss.
近年来,小胶质细胞因其在神经退行性疾病(如青光眼)中发挥不可或缺的作用而受到关注。为了更好地理解小胶质细胞在慢性高眼压过程中的作用,我们使用饮食性集落刺激因子1受体(CSF1R)拮抗剂PLX5622,清除了年龄较大(9至12个月大)的DBA/2J(D2)小鼠体内的小胶质细胞,这些小鼠的眼压会随着年龄增长而升高。对视网膜神经节细胞(RGC)的胞体进行计数,并对视神经横断面进行染色,评估青光眼性损伤情况。持续给予饮食性PLX5622可显著减少视网膜小胶质细胞的数量。饮食性PLX5622不会导致D2或血压正常的DBA/2J-(D2-)对照小鼠眼压发生变化。虽然经PLX5622处理的D2-小鼠未出现视神经损伤,但与喂食对照饮食的D2小鼠相比,经PLX5622处理的D2小鼠中重度视神经损伤显著增加。总之,小胶质细胞的整体减少加剧了D2小鼠的青光眼性神经退行性变,这表明小胶质细胞在保护免受高眼压相关的RGC丢失方面总体上发挥有益作用。