Venanzi Alexander W, McGee Laura D, Hackam Abigail S
Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, 1638 NW 10Th Ave, Rm 404, Miami, FL, 33136, USA.
Mol Neurobiol. 2025 May;62(5):6212-6227. doi: 10.1007/s12035-024-04679-3. Epub 2024 Dec 30.
The optic nerve contains retinal ganglion cell (RGC) axons and functions to transmit visual stimuli to the brain. Injury to the optic nerve from ischemia, trauma, or disease leads to retrograde axonal degeneration and subsequent RGC dysfunction and death, causing irreversible vision loss. Inflammatory responses to neurological damage and axonal injuries in the central nervous system (CNS) are typically harmful to neurons and prevent recovery. However, recent evidence indicates that certain inflammatory cell types and signaling pathways are protective after optic nerve injury and promote RGC survival and axonal regeneration. The objective of this review is to examine the evidence for diverse effects of inflammatory cell types on the retina and optic nerve after injury. Additionally, we highlight promising avenues for further research.
视神经包含视网膜神经节细胞(RGC)轴突,其功能是将视觉刺激传递至大脑。缺血、创伤或疾病对视神经造成的损伤会导致逆行性轴突变性,随后引发RGC功能障碍和死亡,从而导致不可逆的视力丧失。中枢神经系统(CNS)对神经损伤和轴突损伤的炎症反应通常对神经元有害,并会阻碍恢复。然而,最近的证据表明,某些炎症细胞类型和信号通路在视神经损伤后具有保护作用,并能促进RGC存活和轴突再生。本综述的目的是研究炎症细胞类型在损伤后对视网膜和视神经产生不同影响的证据。此外,我们还强调了有前景的进一步研究途径。