Neuron-derived SPP1 instructs microglia to limit degeneration
Neurons actively shape immune responses that maintain central nervous system integrity. We identify SPP1 (secreted phosphoprotein 1) as a neuron-derived signal that reprograms microglia into a neuroprotective, homeostatic state after injury and during neurodegeneration. In mouse models of glaucoma and optic nerve damage, neuronal SPP1 enhances microglial autophagy, debris clearance, and anti-inflammatory activity, preserving neuronal survival and visual function. SPP1 is elevated in neurons of human and primate glaucomatous retinas, where SPP1 + cells show increased resilience. In Alzheimer’s disease brain, neuronal SPP1 correlates with neuronal survival, while microglia around Aβ plaques display defective autophagy. In human iPSC co-cultures, SPP1 enhances microglial Aβ clearance and prevents neurodegeneration. Thus, SPP1 defines a protective neuron–microglia axis in glaucoma and possibly other neurodegenerative diseases.
Authors
- Tatjana Jakobs (ORCID: https://orcid.org/0000-0002-8104-9206)
- Song Li (ORCID: https://orcid.org/0000-0002-0661-4893)
Institutions
- Massachusetts Eye and Ear Infirmary (US)
- Harvard University (US)
- Smith-Kettlewell Eye Research Institute (US)
Publication Details
- Journal
- Science Advances
- Published
- 2026-08-28
- DOI
- https://doi.org/10.1126/sciadv.aee4940
- Primary Topic
- Glaucoma and retinal disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Ellison Medical Foundation
- BrightFocus Foundation
- National Institutes of Health