Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Angiari, S; Rossi, B; Piccio, L; Zinselmeyer, BH; Budui, S; Zenaro, E; Della Bianca, V; Bach, SD; Scarpini, E; Bolomini-Vittori, M; Piacentino, G; Dusi, S; Laudanna, C; Cross, AH; Miller, MJ; Constantin, G.
Regulatory T cells suppress the late phase of the immune response in lymph nodes through P-selectin glycoprotein ligand-1.
J Immunol. 2013; 191(11): 5489-5500. Doi: 10.4049/jimmunol.1301235 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Führende Autor*innen der Med Uni Graz
Angiari Stefano
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
Regulatory T cells (Tregs) maintain tolerance toward self-antigens and suppress autoimmune diseases, although the underlying molecular mechanisms are unclear. In this study, we show that mice deficient for P-selectin glycoprotein ligand-1 (PSGL-1) develop a more severe form of experimental autoimmune encephalomyelitis than wild type animals do, suggesting that PSGL-1 has a role in the negative regulation of autoimmunity. We found that Tregs lacking PSGL-1 were unable to suppress experimental autoimmune encephalomyelitis and failed to inhibit T cell proliferation in vivo in the lymph nodes. Using two-photon laser-scanning microscopy in the lymph node, we found that PSGL-1 expression on Tregs had no role in the suppression of early T cell priming after immunization with Ag. Instead, PSGL-1-deficient Tregs lost the ability to modulate T cell movement and failed to inhibit the T cell-dendritic cell contacts and T cell clustering essential for sustained T cell activation during the late phase of the immune response. Notably, PSGL-1 expression on myelin-specific effector T cells had no role in T cell locomotion in the lymph node. Our data show that PSGL-1 represents a previously unknown, phase-specific mechanism for Treg-mediated suppression of the persistence of immune responses and autoimmunity induction.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Cell Communication - genetics
Cell Growth Processes - genetics
Cell Movement - genetics
Cells, Cultured -
Dendritic Cells - immunology
Disease Progression -
Encephalomyelitis, Autoimmune, Experimental - immunology
Female -
Humans -
Lymph Nodes - pathology
Lymphocyte Activation - genetics
Membrane Glycoproteins - genetics
Membrane Glycoproteins - immunology
Membrane Glycoproteins - metabolism
Mice -
Mice, Inbred C57BL -
Mice, Knockout -
Myelin Sheath - immunology
T-Lymphocyte Subsets - immunology
T-Lymphocytes, Regulatory - immunology

© Med Uni Graz Impressum