Accelerated retinal ganglion cell death in mice deficient in the Sigma-1 receptor
2011

Role of Sigma-1 Receptor in Retinal Cell Protection

Sample size: 10 publication Evidence: high

Author Information

Author(s): Mavlyutov Timur A., Nickells Robert W., Guo Lian-Wang

Primary Institution: University of Wisconsin, School of Medicine and Public Health

Hypothesis

The sigma-1 receptor (σR1) protects retinal ganglion cells from degeneration after optic nerve damage.

Conclusion

The study found that mice lacking the sigma-1 receptor experienced faster retinal ganglion cell death after optic nerve crush, indicating the receptor's protective role.

Supporting Evidence

  • 86.8% of retinal ganglion cells survived in wild-type mice after optic nerve crush.
  • Only 68.3% of retinal ganglion cells survived in sigma-1 receptor knockout mice after the same injury.
  • The sigma-1 receptor was found to be highly expressed in the retinal ganglion cell layer.

Takeaway

Mice without a specific receptor in their eyes lost more nerve cells when their optic nerve was hurt, showing that this receptor helps protect those cells.

Methodology

The study used optic nerve crush to induce retinal ganglion cell death in wild-type and sigma-1 receptor knockout mice, followed by cell counting in retinal whole mounts.

Limitations

The study did not explore other potential protective factors that may also influence retinal ganglion cell survival.

Participant Demographics

Mice were age-matched pairs of 6- and 12-month-old wild-type and sigma-1 receptor knockout mice.

Statistical Information

P-Value

0.0013

Statistical Significance

p=0.0013

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