Imaging regulatory T cell dynamics and CTLA4-mediated suppression of T cell priming.
basic_science · Level V
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- Record sourced from PubMed, PMID 25653051.
- Also identified by DOI 10.1038/ncomms7219 and PMC identifier 4347855.
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Abstract
Foxp3(+) regulatory T cells (Tregs) maintain immune homoeostasis through mechanisms that remain incompletely defined. Here by two-photon (2P) imaging, we examine the cellular dynamics of endogenous Tregs. Tregs are identified as two non-overlapping populations in the T-zone and follicular regions of the lymph node (LN). In the T-zone, Tregs migrate more rapidly than conventional T cells (Tconv), extend longer processes and interact with resident dendritic cells (DC) and Tconv. Tregs intercept immigrant DCs and interact with antigen-induced DC:Tconv clusters, while continuing to form contacts with activated Tconv. During antigen-specific responses, blocking CTLA4-B7 interactions reduces Treg-Tconv interaction times, increases the volume of DC:Tconv clusters and enhances subsequent Tconv proliferation in vivo. Our results demonstrate a role for altered cellular choreography of Tregs through CTLA4-based interactions to limit T-cell priming.
Medical subject headings
- CTLA-4 Antigen
- Dendritic Cells
- Lymph Nodes
- T-Lymphocytes, Regulatory