Department of Ophthalmology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, 83301, Taiwan.
Department of Ophthalmology, Louis J. Fox Center for Vision Restoration, University of Pittsburgh School of Medicine, Pittsburgh, PA, 15219, USA.
Mol Aspects Med. 2023 Dec;94:101219. doi: 10.1016/j.mam.2023.101219. Epub 2023 Oct 13.
Glaucoma is a neurodegenerative eye disease that causes permanent vision impairment. The main pathological characteristics of glaucoma are retinal ganglion cell (RGC) loss and optic nerve degeneration. Glaucoma can be caused by elevated intraocular pressure (IOP), although some cases are congenital or occur in patients with normal IOP. Current glaucoma treatments rely on medicine and surgery to lower IOP, which only delays disease progression. First-line glaucoma medicines are supported by pharmacotherapy advancements such as Rho kinase inhibitors and innovative drug delivery systems. Glaucoma surgery has shifted to safer minimally invasive (or microinvasive) glaucoma surgery, but further trials are needed to validate long-term efficacy. Further, growing evidence shows that adeno-associated virus gene transduction and stem cell-based RGC replacement therapy hold potential to treat optic nerve fiber degeneration and glaucoma. However, better understanding of the regulatory mechanisms of RGC development is needed to provide insight into RGC differentiation from stem cells and help choose target genes for viral therapy. In this review, we overview current progress in RGC development research, optic nerve fiber regeneration, and human stem cell-derived RGC differentiation and transplantation. We also provide an outlook on perspectives and challenges in the field.
青光眼是一种神经退行性眼病,可导致永久性视力损害。青光眼的主要病理特征是视网膜神经节细胞(RGC)丧失和视神经变性。尽管有些病例是先天性的或发生在眼压正常的患者中,但青光眼可能是由眼内压(IOP)升高引起的。目前的青光眼治疗方法依赖于降低 IOP 的药物和手术,这只能延缓疾病的进展。Rho 激酶抑制剂和创新药物输送系统等药物治疗进展支持一线青光眼药物。青光眼手术已转向更安全的微创(或微创新)青光眼手术,但仍需要进一步的试验来验证长期疗效。此外,越来越多的证据表明,腺相关病毒基因转导和基于干细胞的 RGC 替代疗法有可能治疗视神经纤维变性和青光眼。然而,需要更好地了解 RGC 发育的调控机制,以深入了解从干细胞分化为 RGC,并帮助选择病毒治疗的靶基因。在这篇综述中,我们概述了 RGC 发育研究、视神经纤维再生以及人干细胞衍生的 RGC 分化和移植的最新进展。我们还展望了该领域的前景和挑战。