T cell-intrinsic TLR2 stimulation promotes IL-10 expression and suppressive activity by CD45RbHi T cells

Autor: Douglas M. Oswald, Janice C. Jun, Mark B. Jones, Edward S. Sim, Lori S.C. Kreisman, Amruth R. Jonnalagadda, Brian A. Cobb
Jazyk: angličtina
Rok vydání: 2017
Předmět:
0301 basic medicine
CD4-Positive T-Lymphocytes
Male
Physiology
lcsh:Medicine
Immune Receptors
Biochemistry
T-Lymphocytes
Regulatory

White Blood Cells
Spectrum Analysis Techniques
Cell Signaling
Animal Cells
Immune Physiology
Medicine and Health Sciences
Membrane Receptor Signaling
IL-2 receptor
lcsh:Science
Toll-like Receptors
Cells
Cultured

Innate Immune System
Multidisciplinary
Immune System Proteins
TCR signaling cascade
Chemistry
T Cells
FOXP3
Signaling cascades
Regulatory T cells
Flow Cytometry
Immune Receptor Signaling
Cell biology
Interleukin-10
Interleukin 10
medicine.anatomical_structure
Spectrophotometry
Cytokines
Female
Cytophotometry
Cellular Types
Research Article
Signal Transduction
T cell
Immune Cells
Immunology
Receptors
Antigen
T-Cell

chemical and pharmacologic phenomena
Research and Analysis Methods
03 medical and health sciences
Immune system
medicine
Animals
Innate immune system
Blood Cells
lcsh:R
Interleukin-2 Receptor alpha Subunit
Biology and Life Sciences
Proteins
Cell Biology
Molecular Development
Toll-Like Receptor 2
T Cell Receptors
Mice
Inbred C57BL

TLR2
030104 developmental biology
Immune System
Leukocyte Common Antigens
lcsh:Q
Memory T cell
Developmental Biology
Zdroj: PLoS ONE, Vol 12, Iss 7, p e0180688 (2017)
PLoS ONE
ISSN: 1932-6203
Popis: While Toll-like receptors (TLRs) represent one of the best characterized innate immune pathways, evidence suggests that TLRs are not restricted to innate leukocytes and some epithelial cells, but are also expressed in T cells. Specifically, published evidence focusing on FoxP3+ regulatory T cells demonstrate that they express functional TLR2, which is already known among the TLR family for its association with immune suppression; however, little is known about the relationship between T cell-intrinsic TLR2 binding and cytokine production, T cell differentiation, or T cell receptor (TCR) stimulation. Here, we demonstrate that TCR and TLR2 co-stimulation provides a T cell-intrinsic signal which generates a dramatic, synergistic cytokine response dominated by IL-10. Importantly, the response was not seen in either CD4+CD25+ or CD4+FoxP3+ Tregs, yet resulted in the expansion of a suppressive CD4+CD25+CD62L-CD44+CD45Rbhi effector/memory T cell subset not typically associated with immune inhibition. This study reveals the striking ability of a prototypical innate immune receptor to trigger a potent and suppressive IL-10 response in effector/memory T cells, supporting the notion that TLR2 is a co-regulatory receptor on T cells.
Databáze: OpenAIRE