Cyclic adenosine monophosphate is a key component of regulatory T cell–mediated suppression

Author:

Bopp Tobias1,Becker Christian2,Klein Matthias1,Klein-Heßling Stefan3,Palmetshofer Alois3,Serfling Edgar3,Heib Valeska1,Becker Marc1,Kubach Jan2,Schmitt Steffen4,Stoll Sabine2,Schild Hansjörg1,Staege Martin S.5,Stassen Michael1,Jonuleit Helmut2,Schmitt Edgar1

Affiliation:

1. Institute for Immunology

2. Department of Dermatology,

3. Department of Molecular Pathology, Institute of Pathology, University of Würzburg, 97080 Würzburg, Germany

4. Center for Natural Sciences and Medicine, Johannes Gutenberg University, 55131 Mainz, Germany

5. Klinik und Poliklinik für Kinder- und Jugendmedizin, Martin Luther University, 06097 Halle-Wittenberg, Germany

Abstract

Naturally occurring regulatory T cells (T reg cells) are a thymus-derived subset of T cells, which are crucial for the maintenance of peripheral tolerance by controlling potentially autoreactive T cells. However, the underlying molecular mechanisms of this strictly cell contact–dependent process are still elusive. Here we show that naturally occurring T reg cells harbor high levels of cyclic adenosine monophosphate (cAMP). This second messenger is known to be a potent inhibitor of proliferation and interleukin 2 synthesis in T cells. Upon coactivation with naturally occurring T reg cells the cAMP content of responder T cells is also strongly increased. Furthermore, we demonstrate that naturally occurring T reg cells and conventional T cells communicate via cell contact–dependent gap junction formation. The suppressive activity of naturally occurring T reg cells is abolished by a cAMP antagonist as well as by a gap junction inhibitor, which blocks the cell contact–dependent transfer of cAMP to responder T cells. Accordingly, our results suggest that cAMP is crucial for naturally occurring T reg cell–mediated suppression and traverses membranes via gap junctions. Hence, naturally occurring T reg cells unexpectedly may control the immune regulatory network by a well-known mechanism based on the intercellular transport of cAMP via gap junctions.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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