AI Article Synopsis

  • The sigma 2 receptor (σR), also known as transmembrane protein 97 (TMEM97), is linked to neuroprotection and may influence neurodegenerative diseases.
  • Research on TMEM97 mice revealed that their retinal ganglion cells (RGCs) show resistance to degeneration during ischemic conditions, highlighting the protective role of σR/TMEM97.
  • The study supports the potential for developing new neuroprotective treatments for RGC diseases by targeting and inhibiting σR/TMEM97 to prevent cell death.

Article Abstract

The sigma 2 receptor (σR) was recently identified as an endoplasmic reticulum (ER) membrane protein known as transmembrane protein 97 (TMEM97). Studies have shown that σR/TMEM97 binding compounds are neuroprotective, suggesting a role of σR/TMEM97 in neurodegenerative processes. To understand the function of σR/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 σR/TMEM97 ligand DKR-1677 significantly protects RGCs from ischemia-induced degeneration in wildtype mice. Our results provide conclusive evidence that σR/TMEM97 plays a role to facilitate RGC death following ischemic injury and that inhibiting the function of σR/TMEM97 is neuroprotective. This work is a breakthrough toward elucidating the biology and function of σR/TMEM97 in RGCs and likely in other σR/TMEM97 expressing neurons. Moreover, these findings support future studies to develop new neuroprotective approaches for RGC degenerative diseases by inhibiting σR/TMEM97.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9715665PMC
http://dx.doi.org/10.1038/s41598-022-24537-3DOI Listing

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