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Abstract #100703 Published in IGR 23-1
Myocilin Gene Mutation Induced Autophagy Activation Causes Dysfunction of Trabecular Meshwork Cells
Yan X; Wu S; Liu Q; Cheng Y; Zhang J; Wang NFrontiers in cell and developmental biology 2022; 10: 900777
Trabecular meshwork dysfunction is the main cause of primary open angle glaucoma (POAG) associated with elevated intraocular pressure (IOP). Mutant myocilin causes glaucoma mainly via elevating IOP. Previously we have found that accumulated Asn 450 Tyr (N450Y) mutant myocilin impairs human trabecular meshwork (TM) cells by inducing chronic endoplasmic reticulum (ER) stress response . However, it is unclear how ER stress leads to TM damage and whether N450Y myocilin mutation is associated with POAG . Here we found that N450Y mutant myocilin induces autophagy, which worsens cell viability, whereas inhibition of autophagy increases viability and decreases cell death in human TM cells. Furthermore, we construct a transgenic mouse model of N450Y myocilin mutation (Tg-MYOC) and Tg-MYOC mice exhibiting glaucoma phenotypes: IOP elevation, retinal ganglion cell loss and visual impairment. Consistent with our published studies, mutant myocilin fails to secrete into aqueous humor, causes ER stress and actives autophagy in Tg-MYOC mice, and aqueous humor dynamics are altered in Tg-MYOC mice. In summary, our studies demonstrate that activation of autophagy is correlated with pathogenesis of POAG.
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