miR-146a is highly expressed selectively on γδ27− T cells.

Slides:



Advertisements
Similar presentations
Clonal bias of CD56−CD16+ NK cell subpopulations.
Advertisements

Splenic CD169+ macrophages trap and prevent early Lm replication and spread. Splenic CD169+ macrophages trap and prevent early Lm replication and spread.
FIP200 loss links to poor autophagy and high apoptosis in naïve T cells in tumor. FIP200 loss links to poor autophagy and high apoptosis in naïve T cells.
FIP200 deficiency alters mitochondria activation and ROS production in T cells. FIP200 deficiency alters mitochondria activation and ROS production in.
CD8α+ DC-deficient mice are highly susceptible to Lm infection in the absence of CD169+ macrophages. CD8α+ DC-deficient mice are highly susceptible to.
CD169+ macrophages play a critical role in mediating innate immune cell reorganization. CD169+ macrophages play a critical role in mediating innate immune.
Specific depletion of CD4-DTR–derived CD4 T cells.
Three different types of transfer functions with a codomain of [0,1].
Splenic CD169+ macrophages express a unique gene profile.
CCR2+ monocytes are a relevant source of type I IFN in response to Af.
Tfr cells’ transcriptomic profile distinguishes them from Treg and Tfh cells. Tfr cells’ transcriptomic profile distinguishes them from Treg and Tfh cells.
FIP200 controls Bak expression via maintaining microRNA1198-5p expression. FIP200 controls Bak expression via maintaining microRNA1198-5p expression. (A)
Regulatory CD4+ T cell–derived IL-10 is important for B cell differentiation and the GC response. Regulatory CD4+ T cell–derived IL-10 is important for.
Improvement in the transcriptional activity of FOXP3A384T by enhancement of TIP60-FOXP3 interaction. Improvement in the transcriptional activity of FOXP3A384T.
Protein sequence alignment of the NS3 helicase–encoding region of 63 flaviviruses demonstrates conservation of a KIR2DS2-binding peptide. Protein sequence.
Altered distribution of γδT IELs in GPR55-deficient mice.
FIP200 loss links to poor autophagy and high apoptosis in naïve T cells in tumor. FIP200 loss links to poor autophagy and high apoptosis in naïve T cells.
Human PBMC-derived MERS-CoV–specific T cells are multifunctional.
VH usage of cross-reactive B cells induced by H5N1 or H7N9 vaccination
Human cells produce type I and III IFNs upon Af stimulation.
Comparison of repertoire distributions to baseline.
Genetic FIP200 deletion impairs autophagy induction and causes T cell apoptosis. Genetic FIP200 deletion impairs autophagy induction and causes T cell.
β-Glucans do not modulate epithelial IL-33 or AHR.
Tukey boxplots overlaid on data points from objective and subjective measures, displaying results from study 1. Tukey boxplots overlaid on data points.
Tfr cells robustly secrete IL-10 after acute viral infection.
Tfr cell–derived IL-10 is important for B cell differentiation and the GC response. Tfr cell–derived IL-10 is important for B cell differentiation and.
Macrophage-resident NRP1 mitigates cytokine release and proinflammatory polarization. Macrophage-resident NRP1 mitigates cytokine release and proinflammatory.
Definition of the cellular source of IL-22.
Persistent TCR–pMHC-I signaling drives the formation and maintenance of exhausted-like TRM cells. Persistent TCR–pMHC-I signaling drives the formation.
T-bethi MP cells produce IFN-γ in response to IL-12.
TCR signaling is required for exhausted-like TRM cell formation and maintenance. TCR signaling is required for exhausted-like TRM cell formation and maintenance.
Protein sequence alignment of the NS3 helicase–encoding region of 63 flaviviruses demonstrates conservation of a KIR2DS2-binding peptide. Protein sequence.
BAP1 deficiency results in thymic atrophy and loss of thymocyte populations. BAP1 deficiency results in thymic atrophy and loss of thymocyte populations.
Deubiquitinating activity, but not HCF-1 binding, is required for BAP1 function in thymocytes. Deubiquitinating activity, but not HCF-1 binding, is required.
Ag governs CTL behavior at islets but is not required for their accumulation in large numbers. Ag governs CTL behavior at islets but is not required for.
The microbiota inhibits colonic GAPs and antigen delivery after weaning. The microbiota inhibits colonic GAPs and antigen delivery after weaning. (A) Expression.
GPR55 restrains IEL accumulation in the small intestine.
CXCR5+/+ TFH cells are essential for the generation of LCMV-neutralizing antibodies and clearance of a persistent LCMV infection. CXCR5+/+ TFH cells are.
High numbers of non–islet-specific CTLs attenuate effector functions of islet-specific CTLs. High numbers of non–islet-specific CTLs attenuate effector.
BAP1 is required for homeostatic and antigen-driven expansion of peripheral T cells. BAP1 is required for homeostatic and antigen-driven expansion of peripheral.
CD4+CLA+CD103+ T cells from human blood and skin share a transcriptional profile. CD4+CLA+CD103+ T cells from human blood and skin share a transcriptional.
Slc7a5 expression in preosteoclasts is reduced in ovariectomized mice.
CD4+CLA+CD103+ T cells constitute a unique cell population in human blood. CD4+CLA+CD103+ T cells constitute a unique cell population in human blood. (A)
Fig. 2 IT1t prevents TLR7-mediated inflammation in pDCs.
Effects of NAT10 inhibition or depletion on gene expression.
RAPTOR deficiency impairs the DN-to-DP transition in αβ T cell development. RAPTOR deficiency impairs the DN-to-DP transition in αβ T cell development.
Dynamic regulation of cell metabolism and mTORC1 activity and the requirement of RAPTOR in thymocyte development. Dynamic regulation of cell metabolism.
RORα deficiency in Tregs results in exaggerated skin inflammation in response to EC sensitization. RORα deficiency in Tregs results in exaggerated skin.
CD25 expression identifies two transcriptionally distinct subsets of very early effector cells. CD25 expression identifies two transcriptionally distinct.
Loss of BAP1 blocks T cell differentiation at the DN3 stage in vitro.
CD25 surface expression and TCR signal strength predict T helper differentiation and memory potential of early effector T cells in vivo. CD25 surface expression.
Detection of GPR55 ligand in the small intestine.
Tfr cells respond better to immunization with self-antigens than with foreign antigens. Tfr cells respond better to immunization with self-antigens than.
Partial alteration of the Treg gene signature by the p.A384T mutation.
ZIKV-infected Ifnar1+/− fetuses show up-regulated hypoxia response genes just before demise. ZIKV-infected Ifnar1+/− fetuses show up-regulated hypoxia.
CD25 expression predicts effector and memory differentiation.
SLC30A8 and INS gene expression in mTECs and circulating islet-reactive CD8+ T cell frequencies in HLA-A2+ and HLA-A2− healthy donors. SLC30A8 and INS.
GPR55 regulates γδT cell egress from PP and homing of gut-tropic CD8 T cells to the small intestine. GPR55 regulates γδT cell egress from PP and homing.
Tregs preferentially regulate TH2 cytokines in skin.
Bacterial antigen encounter occurs during a specific preweaning interval, is dependent on GCs, and correlates with the presence of colonic GAPs. Bacterial.
Lin28b promotes the positive selection of CD5+ ImmB cells in neonatal mice. Lin28b promotes the positive selection of CD5+ ImmB cells in neonatal mice.
IL-9–expressing TH cells are highly enriched in CCR4+/CCR8+ effector memory TH cells. IL-9–expressing THcells are highly enriched in CCR4+/CCR8+effector.
REV-ERBα deficiency reduces frequency and number of NKp46+ ILC3s.
REV-ERBα deficiency alters the epigenetic landscape and differentially affects clock gene expression in ILC3 subsets. REV-ERBα deficiency alters the epigenetic.
Circadian gene expression in ILC3s is associated with rhythmic cytokine expression. Circadian gene expression in ILC3s is associated with rhythmic cytokine.
Meningeal γδ T cells are biased toward IL-17 production.
Meningeal γδ T cell homeostasis is independent of inflammatory signals
Fetal-derived γδ T cells infiltrate the meninges from birth.
Cartoon model for the increased p-HLA display engendered by peptide splicing. Cartoon model for the increased p-HLA display engendered by peptide splicing.
In response to allergen, T cells and ILCs are equally important sources of IL-13. In response to allergen, T cells and ILCs are equally important sources.
Presentation transcript:

miR-146a is highly expressed selectively on γδ27− T cells. miR-146a is highly expressed selectively on γδ27− T cells. (A) Microarray heat map of differentially expressed miRNAs in duplicate samples of γδ27+ (n = 4 mice per sample) and γδ27−CCR6+ T cells (n = 8 mice per sample) isolated from pooled lymph nodes and spleen of C57BL/6 mice (more than twofold enrichment). (B) RT-qPCR analysis of miR-146a and miR-146b expression in sorted γδ27+ and γδ27− T cells from pooled peripheral organs (lymph node and spleen) of C57BL/6 mice. NS, not significant. (C) RT-qPCR analysis of miR-146a expression in sorted DN2 (CD4−CD8−CD44+CD25+), DN3 (CD4−CD8−CD44−CD25+), γδ25+ (CD25+CD27+), γδ27+, and γδ27− thymocytes of C57BL/6 mice. Results are presented relative to miR-423-3p or RNU5G (reference small RNA) expression. Each symbol in (B) and (C) represents an individual mouse. *P < 0.05 and **P < 0.01 (Mann-Whitney two-tailed test). Nina Schmolka et al. Sci. Immunol. 2018;3:eaao1392 Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works