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σ(2)R/TMEM97 in retinal ganglion cell degeneration
The sigma 2 receptor (σ(2)R) was recently identified as an endoplasmic reticulum (ER) membrane protein known as transmembrane protein 97 (TMEM97). Studies have shown that σ(2)R/TMEM97 binding compounds are neuroprotective, suggesting a role of σ(2)R/TMEM97 in neurodegenerative processes. To understa...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9715665/ https://www.ncbi.nlm.nih.gov/pubmed/36456686 http://dx.doi.org/10.1038/s41598-022-24537-3 |
Sumario: | The sigma 2 receptor (σ(2)R) was recently identified as an endoplasmic reticulum (ER) membrane protein known as transmembrane protein 97 (TMEM97). Studies have shown that σ(2)R/TMEM97 binding compounds are neuroprotective, suggesting a role of σ(2)R/TMEM97 in neurodegenerative processes. To understand the function of σ(2)R/TMEM97 in neurodegeneration pathways, we characterized ischemia-induced retinal ganglion cell (RGC) degeneration in TMEM97(−/−) mice and found that RGCs in TMEM97(−/−) mice are resistant to degeneration. In addition, intravitreal injection of a selective σ(2)R/TMEM97 ligand DKR-1677 significantly protects RGCs from ischemia-induced degeneration in wildtype mice. Our results provide conclusive evidence that σ(2)R/TMEM97 plays a role to facilitate RGC death following ischemic injury and that inhibiting the function of σ(2)R/TMEM97 is neuroprotective. This work is a breakthrough toward elucidating the biology and function of σ(2)R/TMEM97 in RGCs and likely in other σ(2)R/TMEM97 expressing neurons. Moreover, these findings support future studies to develop new neuroprotective approaches for RGC degenerative diseases by inhibiting σ(2)R/TMEM97. |
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