Human “TH9” cells are a subpopulation of PPAR-γ+ TH2 cells

2019 ◽  
Vol 4 (31) ◽  
pp. eaat5943 ◽  
Author(s):  
Claire Micossé ◽  
Leonhard von Meyenn ◽  
Oliver Steck ◽  
Enja Kipfer ◽  
Christian Adam ◽  
...  

Although TH1, TH2, and TH17 cells are well-defined TH cell lineages in humans, it remains debated whether IL-9–producing TH cells represent a bona fide “TH9” lineage. Our understanding of the cellular characteristics and functions of IL-9–producing TH cells in humans is still nascent. Here, we report that human IL-9–producing TH cells express the chemokine receptors CCR4 and CCR8, produce high levels of IL-5 and IL-13, and express TH2 lineage–associated transcription factors. In these cells, IL-9 production is activation dependent, transient, and accompanied by down-regulation of TH2 cytokines, leading to an apparent “TH9” phenotype. IL-9+ TH2 cells can be distinguished from “conventional” TH2 cells based on their expression of the transcription factor PPAR-γ. Accordingly, PPAR-γ is induced in naïve TH cells by priming with IL-4 and TGF-β (“TH9” priming) and is required for IL-9 production. In line with their identity as early activated TH2 cells, IL-9+ TH2 cells are found in acute allergic skin inflammation in humans. We propose that IL-9–producing TH cells are a phenotypically and functionally distinct subpopulation of TH2 cells that depend on PPAR-γ for full effector functions.

Allergy ◽  
2021 ◽  
Author(s):  
Shinsuke Matsuo ◽  
Takashi Hashimoto ◽  
Fumhiro Matsuura ◽  
Osamu Imamura ◽  
Shogo Endo ◽  
...  

1999 ◽  
Vol 189 (12) ◽  
pp. 1987-1992 ◽  
Author(s):  
Hal E. Broxmeyer ◽  
Scott Cooper ◽  
Giao Hangoc ◽  
Ji-Liang Gao ◽  
Philip M. Murphy

Macrophage inflammatory protein (MIP)-1α, a CC chemokine, enhances proliferation of mature subsets of myeloid progenitor cells (MPCs), suppresses proliferation of immature MPCs, and mobilizes mature and immature MPCs to the blood. MIP-1α binds at least three chemokine receptors. To determine if CCR1 was dominantly mediating the above activities of MIP-1α, CCR1-deficient (−/−) mice, produced by targeted gene disruption, were used. MIP-1α enhanced colony formation of marrow granulocyte/macrophage colony-forming units (CFU-GM), responsive to stimulation by granulocyte/macrophage colony-stimulating factor (GM-CSF), and CFU-M, responsive to stimulation by M-CSF, from littermate control CCR1+/+ but not CCR1−/− mice. Moreover, MIP-1α did not mobilize MPCs to the blood or synergize with G-CSF in this effect in CCR1−/− mice. However, CCR1−/− mice were increased in sensitivity to MPC mobilizing effects of G-CSF. Multi-growth factor–stimulated MPCs in CCR1−/− and CCR1+/+ marrow were equally sensitive to inhibition by MIP-1α. These results implicate CCR1 as a dominant receptor for MIP-1α enhancement of proliferation of lineage-committed MPCs and for mobilization of MPCs to the blood. CCR1 is not a dominant receptor for MIP-1α suppression of MPC proliferation, but it does negatively impact G-CSF–induced MPC mobilization.


2019 ◽  
Vol 139 (9) ◽  
pp. 1957-1965.e2 ◽  
Author(s):  
Joerg U. Eberle ◽  
Daniel Radtke ◽  
Falk Nimmerjahn ◽  
David Voehringer

Allergy ◽  
2018 ◽  
Vol 73 (9) ◽  
pp. 1881-1891 ◽  
Author(s):  
Y. Mitamura ◽  
S. Nunomura ◽  
Y. Nanri ◽  
M. Ogawa ◽  
T. Yoshihara ◽  
...  

2002 ◽  
Vol 109 (5) ◽  
pp. 621-628 ◽  
Author(s):  
Weilie Ma ◽  
Paul J. Bryce ◽  
Alison A. Humbles ◽  
Dhafer Laouini ◽  
Ali Yalcindag ◽  
...  

2013 ◽  
Vol 221 ◽  
pp. S132-S133
Author(s):  
Zeina El Ali ◽  
Cédric Gerbeix ◽  
Philippe Esser ◽  
Pauline Robert ◽  
Jean-Jacques Legrand ◽  
...  

2019 ◽  
Vol 48 (3) ◽  
pp. 030006051988944 ◽  
Author(s):  
Yunfu Lv ◽  
Yejuan Li ◽  
Ning Liu ◽  
Yonghong Dong ◽  
Jie Deng

Objectives To evaluate the Th1/Th2 cell profile in spleens of cirrhotic and hypersplenic rats by investigating the expression of Th1-associated chemokine receptors CXCR3, CCR5 and Th2-associated chemokine receptor CCR3. Methods Experimental liver cirrhosis and hypersplenism were induced in rats by the intragastric administration of carbon tetrachloride (CCl4; 40% solution [0.3 ml/100g, twice/week for 8 weeks]) and confirmed by pathology and hemogram. Presence of the three chemokine receptors was investigated by real-time polymerase chain reaction (RT-PCR), immunohistochemical staining, and western blot analysis. Results By comparison with control animals (n=10), RT-PCR demonstrated that CXCR3 and CCR5-mRNA levels were significantly elevated in the hypersplenic rats (n=26) and CCR3-mRNA levels were lower. Immunohistochemical staining showed that by comparison with controls, the mean density of the Th1-associated CXCR3 and CCR5 receptors was significantly increased but there was no difference between groups in Th2-associated CCR3 receptors. Western blot analysis showed that by comparison with controls, hypersplenic rats had higher levels of CXCR3 and CCR5 protein but lower levels of CCR3 protein. Conclusions The abnormal expression of Th1-associated chemokine receptors in spleens of rats with cirrhosis and hypersplenism induced by CCL4 suggests that a functional imbalance between Th1/Th2 cells may play a role in the pathogenesis of hypersplenism.


Allergy ◽  
2019 ◽  
Vol 75 (2) ◽  
pp. 463-467 ◽  
Author(s):  
Keitaro Hayashi ◽  
Osamu Kaminuma ◽  
Tomoe Nishimura ◽  
Mayumi Saeki ◽  
Kunie Matsuoka ◽  
...  

Author(s):  
Tomoaki Koga ◽  
Fumiyuki Sasaki ◽  
Kazuko Saeki ◽  
Soken Tsuchiya ◽  
Toshiaki Okuno ◽  
...  

Abstract Leukotriene B4 (LTB4) receptor 1 (BLT1) is a chemotactic G protein-coupled receptor expressed by leukocytes, such as granulocytes, macrophages, and activated T cells. Although there is growing evidence that BLT1 plays crucial roles in immune responses, its role in dendritic cells remains largely unknown. Here, we identified novel DC subsets defined by the expression of BLT1, namely, BLT1hi and BLT1lo DCs. We also found that BLT1hi and BLT1lo DCs differentially migrated toward LTB4 and CCL21, a lymph node-homing chemoattractant, respectively. By generating LTB4-producing enzyme LTA4H knockout mice and CD11c promoter-driven Cre recombinase-expressing BLT1 conditional knockout (BLT1 cKO) mice, we showed that the migration of BLT1hi DCs exacerbated allergic contact dermatitis. Comprehensive transcriptome analysis revealed that BLT1hi DCs preferentially induced Th1 differentiation by upregulating IL-12p35 expression, whereas BLT1lo DCs accelerated T cell proliferation by producing IL-2. Collectively, the data reveal an unexpected role for BLT1 as a novel DC subset marker and provide novel insights into the role of the LTB4-BLT1 axis in the spatiotemporal regulation of distinct DC subsets.


Sign in / Sign up

Export Citation Format

Share Document