Supporting data for: Caspase-8 expression in CD8+ T cells promotes pathogen restriction in the brain during Toxoplasma gondii infection (MERFISH infected)

Cell death is an integral restriction mechanism against intracellular pathogens. We have previously reported extensive cell death in the brain during infection with the intracellular parasite, Toxoplasma gondii. Here we focus on the role of caspase-8, a regulator of extrinsic apoptosis, during T. gondii infection. We find that Casp8-/-Ripk3-/- mice have increased brain parasite burden in comparison to controls and succumb to infection, despite the generation of robust immune responses. We observed that neurons, astrocytes, and CD8+ T cells had high rates of parasite interactions in Casp8-/-Ripk3-/- mice compared to WT mice. While Casp8 deficiency in neurons and astrocytes did not impact control of infection, deletion of Casp8 in CD8+ T cells led to impaired survival, increased parasite burden and direct infection of CD8+ T cells in the brain. We conclude that in addition to well-characterized effector functions, CD8+ T cells utilize caspase-8 to control T. gondii in the brain.This item contains data for MERFISH (Multiplexed Error-Robust Fluorescence In Situ Hybridization), a single-molecule imaging technique that allows for spatially mapping of single nuclear transcripts. This item contains data for a T. gondii infected brain at 28 dpi including raw data, cell clustering script, cell by gene identification, and detected transcripts.