IL1A enhances TNF-induced retinal ganglion cell death
We identified a novel role of IL1A, we found that IL1A acted as a sensitizer to TNF-induced death. Co-injection of IL1A and TNF resulted in rapid RGC death, with significant RGC loss 14 days after injection. TNF+IL1A-induced RGC death did not depend on JUN activation and was rather SARM1 dependent. Also, RNA-seq analyses indicated that while <i>Sarm1</i> deficiency protected from IL1A+TNF induced RGC loss it did not significantly alter microglia and astrocyte responses. Altogether, these findings indicate that IL1A potentiates SARM1-dependent TNF-induced RGC death <i>in vivo</i>.
Authors
- Katherine M. Andersh (ORCID: https://orcid.org/0000-0001-7709-4111)
- Richard T. Libby (ORCID: https://orcid.org/0000-0003-2844-7632)
- Michael MacLean (ORCID: https://orcid.org/0000-0001-9685-3400)
- Gareth R. Howell
Institutions
- University of Rochester Medical Center (US)
- Jackson Laboratory (US)
- University of Rochester (US)
Publication Details
- Journal
- Frontiers in Aging Neuroscience
- Published
- 2026-02-05
- DOI
- https://doi.org/10.3389/fnagi.2026.1754881
- Primary Topic
- Glaucoma and retinal disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Research to Prevent Blindness
- BrightFocus Foundation
- University of Rochester
- Center for Visual Science