Divergent requirement for Gαs and cAMP in the differentiation and inflammatory profile of distinct mouse Th subsets

Xiangli Li, Fiona Murray, Naoki Koide, Jonathan Goldstone, Sara Dann-Grice, Jianzhong Chen, Samuel Bertin, Guo Fu, Lee S. Weinstein, Min Chen, Maripat Corr, Lars Eckmann, Paul A. Insel, Eyal Raz

Research output: Contribution to journalArticle

32 Citations (Scopus)

Abstract

cAMP, the intracellular signaling molecule produced in response to GPCR signaling, has long been recognized as an immunosuppressive agent that inhibits T cell receptor activation and T cell function. However, recent studies show that cAMP also promotes T cell - mediated immunity. Central to cAMP production downstream of GPCR activation is the trimeric G protein Gs. In order to reconcile the reports of divergent effects of cAMP in T cells and to define the direct effect of cAMP in T cells, we engineered mice in which the stimulatory Gαsubunit of Gs (Gαs) could be deleted in T cells using CD4-Cre (Gnas ΔCD4). Gnas ΔCD4 CD4 + T cells had reduced cAMP accumulation and Ca 2+ influx. In vitro and in vivo, Gnas ΔCD4 CD4 + T cells displayed impaired differentiation to specific Th subsets: Th17 and Th1 cells were reduced or absent, but Th2 and regulatory T cells were unaffected. Furthermore, Gnas ΔCD4 CD4 + T cells failed to provoke colitis in an adoptive transfer model, indicating reduced inflammatory function. Restoration of cAMP levels rescued the impaired phenotype of Gnas ΔCD4CD4 + T cells, reinstated the PKA-dependent influx of Ca 2+, and enhanced the ability of these cells to induce colitis. Our findings thus define an important role for cAMP in the differentiation of Th subsets and their subsequent inflammatory responses, and provide evidence that altering cAMP levels in CD4 + T cells could provide an immunomodulatory approach targeting specific Th subsets.

Original languageEnglish (US)
Pages (from-to)963-973
Number of pages11
JournalJournal of Clinical Investigation
Volume122
Issue number3
DOIs
StatePublished - Mar 1 2012

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T-Lymphocytes
Colitis
Th17 Cells
Th1 Cells
Adoptive Transfer
Regulatory T-Lymphocytes
Immunosuppressive Agents
T-Cell Antigen Receptor
GTP-Binding Proteins
Cellular Immunity
Phenotype

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Divergent requirement for Gαs and cAMP in the differentiation and inflammatory profile of distinct mouse Th subsets. / Li, Xiangli; Murray, Fiona; Koide, Naoki; Goldstone, Jonathan; Dann-Grice, Sara; Chen, Jianzhong; Bertin, Samuel; Fu, Guo; Weinstein, Lee S.; Chen, Min; Corr, Maripat; Eckmann, Lars; Insel, Paul A.; Raz, Eyal.

In: Journal of Clinical Investigation, Vol. 122, No. 3, 01.03.2012, p. 963-973.

Research output: Contribution to journalArticle

Li, X, Murray, F, Koide, N, Goldstone, J, Dann-Grice, S, Chen, J, Bertin, S, Fu, G, Weinstein, LS, Chen, M, Corr, M, Eckmann, L, Insel, PA & Raz, E 2012, 'Divergent requirement for Gαs and cAMP in the differentiation and inflammatory profile of distinct mouse Th subsets', Journal of Clinical Investigation, vol. 122, no. 3, pp. 963-973. https://doi.org/10.1172/JCI59097
Li, Xiangli ; Murray, Fiona ; Koide, Naoki ; Goldstone, Jonathan ; Dann-Grice, Sara ; Chen, Jianzhong ; Bertin, Samuel ; Fu, Guo ; Weinstein, Lee S. ; Chen, Min ; Corr, Maripat ; Eckmann, Lars ; Insel, Paul A. ; Raz, Eyal. / Divergent requirement for Gαs and cAMP in the differentiation and inflammatory profile of distinct mouse Th subsets. In: Journal of Clinical Investigation. 2012 ; Vol. 122, No. 3. pp. 963-973.
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AU - Fu, Guo

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