A forskolin-mediated increase in cAMP promotes T helper cell
differentiation into the Th1 and Th2 subsets rather than into
the Th17 subset

J 2023

A forskolin-mediated increase in cAMP promotes T helper cell differentiation into the Th1 and Th2 subsets rather than into the Th17 subset

DAĎOVÁ, Petra; Antónia MIKULOVÁ; Radim JAROUŠEK; Michaela CHORVÁTOVÁ; Stjepan ULDRIJAN et. al.

Základní údaje

Originální název

A forskolin-mediated increase in cAMP promotes T helper cell differentiation into the Th1 and Th2 subsets rather than into the Th17 subset

Autoři

DAĎOVÁ, Petra; Antónia MIKULOVÁ; Radim JAROUŠEK; Michaela CHORVÁTOVÁ; Stjepan ULDRIJAN a Lukáš KUBALA

Vydání

International Immunopharmacology, Elsevier, 2023, 1567-5769

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10608 Biochemistry and molecular biology

Stát vydavatele

Nizozemské království

Utajení

není předmětem státního či obchodního tajemství

Odkazy

URL

Impakt faktor

Impact factor: 4.800

Kód RIV

RIV/00216224:14310/23:00133100

Organizační jednotka

Přírodovědecká fakulta

DOI

https://doi.org/10.1016/j.intimp.2023.111166

UT WoS

001112358600001

EID Scopus

2-s2.0-85176617007

Klíčová slova anglicky

DEPENDENT PROTEIN-KINASE; CYCLIC-AMP; GENETIC ARCHITECTURE; PDE4 INHIBITOR; RESPONSES; MEMORY; NAIVE; LYMPHOCYTES; EXPRESSION; MODULATORS

Štítky

14110513, 14314010, podil, rivok

Příznaky

Mezinárodní význam, Recenzováno

Změněno: 12. 3. 2024 12:56, Mgr. Marie Novosadová Šípková, DiS.

Anotace

V originále

The adenylyl cyclase (AC) signaling pathway is suggested to be a key regulator of immune system functions. However, specific effects of cyclic adenosine mono -phosphate (cAMP) on T helper (Th) cell differentiation and functions are unclear. The involvement of cAMP in the Th cell differentiation program, in particular the development of Th1, Th2, and Th17 subsets, was evaluated employing forskolin (FSK), a labdane diterpene well known as an AC activator. FSK mediated an elevation in Th1-specific markers reinforcing the Th1 cell phenotype. The Th2 differentiation was supported by FSK, though cell metabolism was negatively affected. In contrast, the Th17 immunophenotype was severely suppressed leading to the highly specific upregulation of CXCL13. The causality between FSK-elicited cAMP production and the observed reinforcement of Th2 differentiation was established by using AC inhibitor 2 ',5 '-dideoxyadenosine, which reverted the FSK effects. Overall, an FSK-mediated cAMP increase affects Th1, Th2 and Th17 differentiation and can contribute to the identification of novel therapeutic targets for the treatment of Th cell-related pathological processes.

Návaznosti

EF16_025/0007381, projekt VaV

Název: Preklinická progrese nových organických sloučenin s cílenou biologickou aktivitou

MUNI/A/1393/2022, interní kód MU

Název: Biomedicínské vědy III

Investor: Masarykova univerzita, Biomedicínské vědy III

Citovat

DAĎOVÁ, Petra; Antónia MIKULOVÁ; Radim JAROUŠEK; Michaela CHORVÁTOVÁ; Stjepan ULDRIJAN a Lukáš KUBALA. A forskolin-mediated increase in cAMP promotes T helper cell differentiation into the Th1 and Th2 subsets rather than into the Th17 subset. International Immunopharmacology. Elsevier, 2023, roč. 125, December, s. 1-15. ISSN 1567-5769. Dostupné z: https://doi.org/10.1016/j.intimp.2023.111166.

@article{2362940,
   author = {Daďová, Petra and Mikulová, Antónia and Jaroušek, Radim and Chorvátová, Michaela and Uldrijan, Stjepan and Kubala, Lukáš},
   article_number = {December},
   doi = {https://doi.org/10.1016/j.intimp.2023.111166},
   keywords = {DEPENDENT PROTEIN-KINASE; CYCLIC-AMP; GENETIC ARCHITECTURE; PDE4 INHIBITOR; RESPONSES; MEMORY; NAIVE; LYMPHOCYTES; EXPRESSION; MODULATORS},
   language = {eng},
   issn = {1567-5769},
   journal = {International Immunopharmacology},
   title = {A forskolin-mediated increase in cAMP promotes T helper cell differentiation into the Th1 and Th2 subsets rather than into the Th17 subset},
   url = {https://www.sciencedirect.com/science/article/pii/S1567576923014923},
   volume = {125},
   year = {2023}
}

TY  - JOUR
ID  - 2362940
AU  - Daďová, Petra - Mikulová, Antónia - Jaroušek, Radim - Chorvátová, Michaela - Uldrijan, Stjepan - Kubala, Lukáš
PY  - 2023
TI  - A forskolin-mediated increase in cAMP promotes T helper cell differentiation into the Th1 and Th2 subsets rather than into the Th17 subset
JF  - International Immunopharmacology
VL  - 125
IS  - December
SP  - 1-15
EP  - 1-15
PB  - Elsevier
SN  - 15675769
KW  - DEPENDENT PROTEIN-KINASE
KW  - CYCLIC-AMP
KW  - GENETIC ARCHITECTURE
KW  - PDE4 INHIBITOR
KW  - RESPONSES
KW  - MEMORY
KW  - NAIVE
KW  - LYMPHOCYTES
KW  - EXPRESSION
KW  - MODULATORS
UR  - https://www.sciencedirect.com/science/article/pii/S1567576923014923
N2  - The adenylyl cyclase (AC) signaling pathway is suggested to be a key regulator of immune system functions. However, specific effects of cyclic adenosine mono -phosphate (cAMP) on T helper (Th) cell differentiation and functions are unclear. The involvement of cAMP in the Th cell differentiation program, in particular the development of Th1, Th2, and Th17 subsets, was evaluated employing forskolin (FSK), a labdane diterpene well known as an AC activator. FSK mediated an elevation in Th1-specific markers reinforcing the Th1 cell phenotype. The Th2 differentiation was supported by FSK, though cell metabolism was negatively affected. In contrast, the Th17 immunophenotype was severely suppressed leading to the highly specific upregulation of CXCL13. The causality between FSK-elicited cAMP production and the observed reinforcement of Th2 differentiation was established by using AC inhibitor 2 ',5 '-dideoxyadenosine, which reverted the FSK effects. Overall, an FSK-mediated cAMP increase affects Th1, Th2 and Th17 differentiation and can contribute to the identification of novel therapeutic targets for the treatment of Th cell-related pathological processes.
ER  -

DAĎOVÁ, Petra; Antónia MIKULOVÁ; Radim JAROUŠEK; Michaela CHORVÁTOVÁ; Stjepan ULDRIJAN a Lukáš KUBALA. A forskolin-mediated increase in cAMP promotes T helper cell differentiation into the Th1 and Th2 subsets rather than into the Th17 subset. \textit{International Immunopharmacology}. Elsevier, 2023, roč.~125, December, s.~1-15. ISSN~1567-5769. Dostupné z: https://doi.org/10.1016/j.intimp.2023.111166.

Přehled o publikaci