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.
Skip Nav Destination
Article navigation
11 June 2007
Brief Definitive Report|
May 14 2007
Cyclic adenosine monophosphate is a key component of regulatory T cell–mediated suppression
Christian Becker,
Christian Becker
2Department of Dermatology,
Search for other works by this author on:
Stefan Klein-Heßling,
Stefan Klein-Heßling
4Department of Molecular Pathology, Institute of Pathology, University of Würzburg, 97080 Würzburg, Germany
Search for other works by this author on:
Alois Palmetshofer,
Alois Palmetshofer
4Department of Molecular Pathology, Institute of Pathology, University of Würzburg, 97080 Würzburg, Germany
Search for other works by this author on:
Edgar Serfling,
Edgar Serfling
4Department of Molecular Pathology, Institute of Pathology, University of Würzburg, 97080 Würzburg, Germany
Search for other works by this author on:
Steffen Schmitt,
Steffen Schmitt
3Center for Natural Sciences and Medicine, Johannes Gutenberg University, 55131 Mainz, Germany
Search for other works by this author on:
Hansjörg Schild,
Hansjörg Schild
1Institute for Immunology
Search for other works by this author on:
Martin S. Staege,
Martin S. Staege
5Klinik und Poliklinik für Kinder- und Jugendmedizin, Martin Luther University, 06097 Halle-Wittenberg, Germany
Search for other works by this author on:
Michael Stassen,
Michael Stassen
1Institute for Immunology
Search for other works by this author on:
Helmut Jonuleit,
Helmut Jonuleit
2Department of Dermatology,
Search for other works by this author on:
Edgar Schmitt
Edgar Schmitt
1Institute for Immunology
Search for other works by this author on:
Tobias Bopp
1Institute for Immunology
Christian Becker
2Department of Dermatology,
Matthias Klein
1Institute for Immunology
Stefan Klein-Heßling
4Department of Molecular Pathology, Institute of Pathology, University of Würzburg, 97080 Würzburg, Germany
Alois Palmetshofer
4Department of Molecular Pathology, Institute of Pathology, University of Würzburg, 97080 Würzburg, Germany
Edgar Serfling
4Department of Molecular Pathology, Institute of Pathology, University of Würzburg, 97080 Würzburg, Germany
Valeska Heib
1Institute for Immunology
Marc Becker
1Institute for Immunology
Jan Kubach
2Department of Dermatology,
Steffen Schmitt
3Center for Natural Sciences and Medicine, Johannes Gutenberg University, 55131 Mainz, Germany
Sabine Stoll
2Department of Dermatology,
Hansjörg Schild
1Institute for Immunology
Martin S. Staege
5Klinik und Poliklinik für Kinder- und Jugendmedizin, Martin Luther University, 06097 Halle-Wittenberg, Germany
Michael Stassen
1Institute for Immunology
Helmut Jonuleit
2Department of Dermatology,
Edgar Schmitt
1Institute for Immunology
CORRESPONDENCE Edgar Schmitt: [email protected]
Received:
October 04 2006
Accepted:
April 24 2007
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2007
J Exp Med (2007) 204 (6): 1303–1310.
Article history
Received:
October 04 2006
Accepted:
April 24 2007
Connected Content
Related
cAMP crosses junctions
Citation
Tobias Bopp, Christian Becker, Matthias Klein, Stefan Klein-Heßling, Alois Palmetshofer, Edgar Serfling, Valeska Heib, Marc Becker, Jan Kubach, Steffen Schmitt, Sabine Stoll, Hansjörg Schild, Martin S. Staege, Michael Stassen, Helmut Jonuleit, Edgar Schmitt; Cyclic adenosine monophosphate is a key component of regulatory T cell–mediated suppression . J Exp Med 11 June 2007; 204 (6): 1303–1310. doi: https://doi.org/10.1084/jem.20062129
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
See also
Email alerts
Advertisement