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CD8+ T cells localize preferentially to cerebral vasculature and promote fatal vascular breakdown during ECM.

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posted on 2016-12-01, 04:30 authored by Phillip A. Swanson II, Geoffrey T. Hart, Matthew V. Russo, Debasis Nayak, Takele Yazew, Mirna Peña, Shahid M. Khan, Chris J. Janse, Susan K. Pierce, Dorian B. McGavern

(A) Survival curve showing PbA-infected wild type (black line), CD4+ T cell depleted (red line), and CD8+ T cell depleted (green line) mice over time (n = 4–5 mice per group). CD8+ or CD4+ T cells were depleted by injecting anti-CD8 or CD4 antibodies, respectively, at d4 p.i. (B) Representative maximal projections of 3D time lapses captured through a thinned skull window and the corresponding ear of a wild type mouse seeded i.v. with 104 naïve mCerulean+ OT-I cells (green) and then infected one day later PbA-OVA-mCherry. Time lapses were captured at d6 p.i. Blood vessels are shown red (n = 7 mice per group). See corresponding S5S7 Movies. (C) Maximal projections captured through a thinned skull window depicting OT-I cells (green), blood vessels (red), and a volumetric mask corresponding to the vascular quantum dot signal (gray). Each row represents a different mouse. See corresponding S8 Movie. (D) Pie graph showing the percentage of luminal vs. extravascular OT-I cells at day 6 p.i. (mean ±SD; n = 5 mice). All data in this figure are representative of two independent experiments. Asterisks denote statistical significance (*P < 0.05).

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