Glial cell-mediated spread of retinal degeneration during detachment: A hypothesis based upon studies in rabbits
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Abstract
In human subjects with peripheral retinal detachments, visual deficits are not restricted to the detached retina but are also present in the non-detached tissue. Based upon studies on a rabbit model of rhegmatogenous retinal detachment, we propose a glial cell-mediated mechanism of spread of retinal degeneration into non-detached retinal areas which may also have importance for the understanding of alterations in the human retina. Both detached and attached portions of the rabbit retina display photoreceptor cell degeneration and cystic degeneration of the innermost layers. An inverse mode of photoreceptor cell degeneration in the attached tissue suggests a disturbed support of the photoreceptor cells by Müller cells which show various indications of gliosis (increased expression of intermediate filaments, cell hypertrophy, decreased plasma membrane K+ conductance, increased Ca2+ responsiveness to purinergic stimulation) in both detached and attached tissues. We propose that gliotic alterations of Müller cells contribute to the degeneration of the attached retina, via disturbance of glial homeostasis mechanisms. A down-regulation of the K+ conductance of Müller cells may prevent effective retinal K+ and water clearance, and may favor photoreceptor cell degeneration and edema development.
Details
| Original language | English |
|---|---|
| Pages (from-to) | 2256-2267 |
| Number of pages | 12 |
| Journal | Vision Research |
| Volume | 45 |
| Issue number | 17 |
| Publication status | Published - Aug 2005 |
| Peer-reviewed | Yes |
| Externally published | Yes |
External IDs
| PubMed | 15924940 |
|---|
Keywords
ASJC Scopus subject areas
Keywords
- Edema, Müller's glia, P2 receptors, Photoreceptors, Potassium channels, Retinal detachment