Gαs-coupled receptor signaling and sleep regulate integrin activation of human antigen-specific T cells
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Standard
Gαs-coupled receptor signaling and sleep regulate integrin activation of human antigen-specific T cells. / Dimitrov, Stoyan; Lange, Tanja; Gouttefangeas, Cécile; Jensen, Anja T R; Szczepanski, Michael; Lehnnolz, Jannik; Soekadar, Surjo; Rammensee, Hans-Georg; Born, Jan; Besedovsky, Luciana.
I: The Journal of Experimental Medicine, Bind 216, Nr. 3, 2019, s. 517-526.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
APA
Vancouver
Author
Bibtex
}
RIS
TY - JOUR
T1 - Gαs-coupled receptor signaling and sleep regulate integrin activation of human antigen-specific T cells
AU - Dimitrov, Stoyan
AU - Lange, Tanja
AU - Gouttefangeas, Cécile
AU - Jensen, Anja T R
AU - Szczepanski, Michael
AU - Lehnnolz, Jannik
AU - Soekadar, Surjo
AU - Rammensee, Hans-Georg
AU - Born, Jan
AU - Besedovsky, Luciana
PY - 2019
Y1 - 2019
N2 - Efficient T cell responses require the firm adhesion of T cells to their targets, e.g., virus-infected cells, which depends on T cell receptor (TCR)-mediated activation of β2-integrins. Gαs-coupled receptor agonists are known to have immunosuppressive effects, but their impact on TCR-mediated integrin activation is unknown. Using multimers of peptide major histocompatibility complex molecules (pMHC) and of ICAM-1-the ligand of β2-integrins-we show that the Gαs-coupled receptor agonists isoproterenol, epinephrine, norepinephrine, prostaglandin (PG) E2, PGD2, and adenosine strongly inhibit integrin activation on human CMV- and EBV-specific CD8+ T cells in a dose-dependent manner. In contrast, sleep, a natural condition of low levels of Gαs-coupled receptor agonists, up-regulates integrin activation compared with nocturnal wakefulness, a mechanism possibly underlying some of the immune-supportive effects of sleep. The findings are also relevant for several pathologies associated with increased levels of Gαs-coupled receptor agonists (e.g., tumor growth, malaria, hypoxia, stress, and sleep disturbances).
AB - Efficient T cell responses require the firm adhesion of T cells to their targets, e.g., virus-infected cells, which depends on T cell receptor (TCR)-mediated activation of β2-integrins. Gαs-coupled receptor agonists are known to have immunosuppressive effects, but their impact on TCR-mediated integrin activation is unknown. Using multimers of peptide major histocompatibility complex molecules (pMHC) and of ICAM-1-the ligand of β2-integrins-we show that the Gαs-coupled receptor agonists isoproterenol, epinephrine, norepinephrine, prostaglandin (PG) E2, PGD2, and adenosine strongly inhibit integrin activation on human CMV- and EBV-specific CD8+ T cells in a dose-dependent manner. In contrast, sleep, a natural condition of low levels of Gαs-coupled receptor agonists, up-regulates integrin activation compared with nocturnal wakefulness, a mechanism possibly underlying some of the immune-supportive effects of sleep. The findings are also relevant for several pathologies associated with increased levels of Gαs-coupled receptor agonists (e.g., tumor growth, malaria, hypoxia, stress, and sleep disturbances).
U2 - 10.1084/jem.20181169
DO - 10.1084/jem.20181169
M3 - Journal article
C2 - 30755455
VL - 216
SP - 517
EP - 526
JO - The Journal of Experimental Medicine
JF - The Journal of Experimental Medicine
SN - 0022-1007
IS - 3
ER -
ID: 214991267