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Müller cell activation, proliferation and migration following laser injury. | LitMetric

AI Article Synopsis

  • Müller cells are crucial for retinal health, but their response to injury and role in retinal repair need more research; this study explores how they react to retinal damage through a specific mouse model.
  • The study induced localized retinal injuries using laser photocoagulation in young mice and evaluated the Müller cell response via protein analysis and live cell imaging.
  • Findings showed that Müller cells become reactive and migrate toward the injury site, indicating they participate in retinal repair, but no evidence of their conversion into other cell types was found.

Article Abstract

Purpose: Müller cells are well known for their critical role in normal retinal structure and function, but their reaction to retinal injury and subsequent role in retinal remodeling is less well characterized. In this study we used a mouse model of retinal laser photocoagulation to examine injury-induced Müller glial reaction, and determine how this reaction was related to injury-induced retinal regeneration and cellular repopulation.

Methods: Experiments were performed on 3-4-week-old C57BL/6 mice. Retinal laser photocoagulation was used to induce small, circumscribed injuries; these were principally confined to the outer nuclear layer, and surrounded by apparently healthy retinal tissue. Western blotting and immunohistochemical analyses were used to determine the level and location of protein expression. Live cell imaging of green fluorescent protein (GFP)-infected Müller cells (AAV-GFAP-GFP) were used to identify the rate and location of retinal Müller cell nuclear migration.

Results: Upon injury, Müller cells directly at the burn site become reactive, as evidenced by increased expression of the intermediate filament proteins glial fibrillary acidic protein (GFAP) and nestin. These reactive cells re-enter the cell cycle as shown by expression of the markers Cyclin D1 and D3, and their nuclei begin to migrate toward the injury site at a rate of approximately 12 microm/hr. However, unlike other reports, evidence for Müller cell transdifferentiation was not identified in this model.

Conclusions: Retinal laser photocoagulation is capable of stimulating a significant glial reaction, marked by activation of cell cycle progression and retinal reorganization, but is not capable of stimulating cellular transdifferentiation or neurogenesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2746266PMC

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