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

Tobias Bopp(Institute of Immunology), Christian Becker, Matthias Klein(Institute of Immunology), Stefan Klein‐Hessling(University of Würzburg), Alois Palmetshofer(University of Würzburg), Edgar Serfling(University of Würzburg), Valeska Heib(Institute of Immunology), Marc A. Becker(Institute of Immunology), Jan Kubach, Steffen Schmitt(Johannes Gutenberg University Mainz), Sabine Stoll, Hansjörg Schild(Institute of Immunology), Martin S. Staege(Klinik und Poliklinik für Kinder- und Jugendmedizin), Michael Stassen(Institute of Immunology), Helmut Jonuleit, Edgar Schmitt(Institute of Immunology)
The Journal of Experimental Medicine
May 14, 2007
Cited by 635Open Access
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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.


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