A broad perspective on the molecular regulation of retinal ganglion cell degeneration in glaucoma

被引:13
作者
Tezel, Gulgun [1 ]
机构
[1] Columbia Univ, Dept Ophthalmol, Edward S Harkness Eye Inst, Vagelos Coll Phys & Surg, New York, NY 10027 USA
来源
GLAUCOMA: A NEURODEGENERATIVE DISEASE OF THE RETINA AND BEYOND - PT A | 2020年 / 256卷
关键词
Glaucoma; Molecular signaling; Neurodegeneration; Neuroinflammation; Optic nerve axons; Retinal ganglion cells; OPTIC-NERVE HEAD; LATERAL GENICULATE-NUCLEUS; NECROSIS-FACTOR-ALPHA; NITRIC-OXIDE SYNTHASE; MOUSE MODEL; OXIDATIVE STRESS; LAMINA-CRIBROSA; IMMUNOHISTOCHEMICAL ASSESSMENT; INFLAMMATORY RESPONSES; AXONAL DEGENERATION;
D O I
10.1016/bs.pbr.2020.05.027
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Glaucoma is a complex neurodegenerative disease involving RGC axons, somas, and synapses at dendrites and axon terminals. Recent research advancements in the field have revealed a bigger picture of glaucomatous neurodegeneration that encompasses multiple stressors, multiple injury sites, multiple cell types, and multiple signaling pathways for asynchronous degeneration of RGCs during a chronic disease period. Optic nerve head is commonly viewed as the critical site of injury in glaucoma, where early injurious insults initiate distal and proximal signaling for axonal and somatic degeneration. Despite compartmentalized processes for degeneration of RGC axons and somas, there are intricate interactions between the two compartments and mechanistic overlaps between the molecular pathways that mediate degeneration in axonal and somatic compartments. This review summarizes the recent progress in the molecular understanding of RGC degeneration in glaucoma and highlights various etiological paths with biomechanical, metabolic, oxidative, and inflammatory components. Through this growing body of knowledge, the glaucoma community moves closer toward causative treatment of this blinding disease.
引用
收藏
页码:49 / 77
页数:29
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