Early retinal microglial activation and ganglion cell dysfunction following severe traumatic brain injury in mice

Authors

Pentek, L., Czeiter, E., Amrein, K., Szentivanyi, A., Kovacs, B., Balogh, B., Szarka, G., Volgyi, B., Kovacs-Oller, T.

Abstract

Traumatic brain injury (TBI) induces rapid neuroinflammatory responses not only in the brain but also in anatomically and immunologically connected central nervous system (CNS) compartments, including the retina. In our study, we investigated retinal microglial activation, retinal ganglion cell (RGC) calcium dynamics, and caspase3 activation in adult mice subjected to severe traumatic brain injury using the Marmarou impact acceleration model at 24 and 48 h post-injury. Carrying out Ca2+ imaging, immunohistochemistry, and ex vivo lapse microscopy, we found robust microglial activation in both the superficial and deep retinal layers following TBI, accompanied by increased microglial motility. RGCs exhibited a transient surge in degeneration-induced spontaneous activity at 24 h, followed by a marked reduction below control levels at 48 h, consistent with early degenerative changes. Activated caspase3 levels were significantly elevated in both microglia and other retinal cell types at both time points, indicating ongoing apoptotic effects. Together, these findings demonstrate that TBI rapidly triggers inflammatory and apoptotic mechanisms in the retina, which are detectable within the first 48 hours. Our results highlight the retina as a sensitive indicator of early CNS pathology after traumatic injury and underscore the potential of retinal analysis for monitoring TBI-induced neurodegeneration for future clinical implementation.

Preprint server: bioRxiv
The authors list and abstract were imported from bioRxiv on 02 Jul 2026.

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