Evidence map›Paper›PMID 27548145›Full record

ArticleInternational journal of molecular sciences2016

Sex-Based Selectivity of PPARγ Regulation in Th1, Th2, and Th17 Differentiation.

Hong-Jai Park, Hyeon-Soo Park, Jae-Ung Lee, Alfred L M Bothwell, Je-Min Choi

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
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  3. Biomedicines · 2025
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  12. Ozonated autohemotherapy elevates PPAR-γ expression in CD4American journal of translational research · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Hong-Jai ParkDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 04763, Korea. hongjai@hanyang.ac.kr.
Hyeon-Soo ParkDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 04763, Korea. hspark91@hanyang.ac.kr.
Jae-Ung LeeDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 04763, Korea. jaeunglee@hanyang.ac.kr.
Alfred L M BothwellDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 06520, USA. alfred.bothwell@yale.edu.
Je-Min ChoiDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 04763, Korea. jeminchoi@hanyang.ac.kr.
Hanyang University · KRInstitute for Basic Science · KRYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI DAVID L RIMM · 1985 to 2026
$85.0M
NCATS NIH HHS UL1 TR001863NCI NIH HHS P30 CA016359
6 · The paper itself

Abstract

Peroxisome proliferator-activated receptor gamma (PPARγ) has recently been recognized to regulate adaptive immunity through Th17 differentiation, Treg functions, and TFH responses. However, its role in adaptive immunity and autoimmune disease is still not clear, possibly due to sexual differences. Here, we investigated in vitro treatment study with the PPARγ agonist pioglitazone to compare Th1, Th2, and Th17 differentiation in male and female mouse splenic T cells. Pioglitazone treatment significantly inhibited various effector T cell differentiations including Th1, Th2, and Th17 cells from female naïve T cells, but it selectively reduced IL-17 production in male Th17 differentiation. Interestingly, pioglitazone and estradiol (E2) co-treatment of T cells in males inhibited differentiation of Th1, Th2, and Th17 cells, suggesting a mechanism for the greater sensitivity of PPARγ to ligand treatment in the regulation of effector T cell differentiation in females. Collectively, these results demonstrate that PPARγ selectively inhibits Th17 differentiation only in male T cells and modulates Th1, Th2, and Th17 differentiation in female T cells based on different level of estrogen exposure. Accordingly, PPARγ could be an important immune regulator of sexual differences in adaptive immunity.

Indexed as

AnimalsCell DifferentiationCells, CulturedEstrogensFemaleMaleMiceMice, Inbred C57BLPioglitazonePPAR gammaSex FactorsTh17 CellsTh1 CellsTh2 CellsThiazolidinedionesEstrogensPioglitazonePPAR gammaThiazolidinedioneseffector T cellsestrogenpioglitazonePPARγsex

Identifiers

PMID27548145
PMCPMC5000743
OpenAlexW2513413220

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.