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Flotillin-2 dampens T cell antigen sensitivity and functionality
Sookjin Moon, Fei Zhao, Mohammad N. Uddin, Charles J. Tucker, Peer W.F. Karmaus, Michael B. Fessler
Sookjin Moon, Fei Zhao, Mohammad N. Uddin, Charles J. Tucker, Peer W.F. Karmaus, Michael B. Fessler
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Research Article Immunology

Flotillin-2 dampens T cell antigen sensitivity and functionality

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Abstract

T cell receptor (TCR) engagement triggers T cell responses, yet how TCR-mediated activation is regulated at the plasma membrane remains unclear. Here, we report that deleting the membrane scaffolding protein Flotillin-2 (Flot2) increases T cell antigen sensitivity, resulting in enhanced TCR signaling and effector function in response to weak TCR stimulation. T cell–specific Flot2-deficient mice exhibited reduced tumor growth and enhanced immunity to infection. Flot2-null CD4+ T cells exhibited increased Th1 polarization, proliferation, Nur77 induction, and phosphorylation of ZAP70 and ERK1/2 upon weak TCR stimulation, indicating a sensitized TCR-triggering threshold. Single-cell RNA-Seq suggested that Flot2-null CD4+ T cells follow a similar route of activation as WT CD4+ T cells but exhibit higher occupancy of a discrete activation state under weak TCR stimulation. Given prior reports that TCR clustering influences sensitivity of T cells to stimuli, we evaluated TCR distribution with super-resolution microscopy. Flot2 ablation increased the number of surface TCR nanoclusters on naive CD4+ T cells. Collectively, we posit that Flot2 modulates T cell functionality to weak TCR stimulation, at least in part, by regulating surface TCR clustering. Our findings have implications for improving T cell reactivity in diseases with poor antigenicity, such as cancer and chronic infections.

Authors

Sookjin Moon, Fei Zhao, Mohammad N. Uddin, Charles J. Tucker, Peer W.F. Karmaus, Michael B. Fessler

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Figure 3

Flot2 deficiency promotes CD4+ and CD8+ T cell responses against Listeria monocytogenes infection.

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Flot2 deficiency promotes CD4+ and CD8+ T cell responses against Listeri...
(A) Weight loss in Flot2+/+ or Flot2–/– mice following Listeria monocytogenes infection (5,000 CFU per mouse) is presented as the mean percentage of initial weight (n = 4–5 per group). (B–G) Flow cytometric analysis of splenic T cells from Listeria-infected Flot2+/+ or Flot2–/– mice. Representative plots (B and E) are provided. CD44+Ki67+ (C) and TNF-α+ (D) populations within viable CD45+TCRβ+CD4+ population and CD44+Ki67+ (F) and TNF-α+ (G) populations within viable CD45+TCRβ+CD8+ population are shown. (H) Weight loss in Flot2WT or Flot2CD4 mice following L. monocytogenes infection (5,000 CFU per mouse) is presented as the mean percentage of initial weight (n = 5–6 per group). (I) Splenic CD4+ and CD8+ T cells numbers in infected Flot2WT or Flot2CD4 mice are depicted. (J–Q) Flow cytometric analysis of splenic T cells from L. monocytogenes–infected Flot2WT or Flot2CD4 mice. Representative plots (J, L, and O) are shown. TNF-α+IFN-γ+IL-2+ (K), CD44+Ki67+ (M), and TNF-α+ (N) populations within viable CD45+TCRβ+CD4+ population and CD44+Ki67+ (P) and TNF-α+ (Q) populations within viable CD45+TCRβ+CD8+ population are shown. Data are representative of 2 independent experiments (A–Q). Data were analyzed by unpaired t test (C, D, F, G, I, K, M, N, P, and Q) or 2-way ANOVA followed with Šidák’s multiple-comparison tests (A and H). Data are shown as mean ± SEM; *P < 0.05; **P < 0.01; ***P < 0.001.

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