Evidence map›Paper›PMID 32868763›Full record

ArticleNature communications2020

Single-cell RNA sequencing identifies shared differentiation paths of mouse thymic innate T cells.

Minji Lee, Eunmin Lee, Seong Kyu Han, Yoon Ha Choi, Dong-Il Kwon, Hyobeen Choi, Kwanghwan Lee, Eun Seo Park, Min-Seok Rha, Dong Jin Joo and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
–field-weighted citation impact
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

60 citing papers in PubMed.

  1. Article
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  4. Review
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  6. Article
  7. Review
  8. Metabolic control of innate-like T cells.Nature reviews. Immunology · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Innateness transcriptome gradients characterize mouse T lymphocyte populations.Journal of immunology (Baltimore, Md. : 1950) · 2025
    Article
  16. Article
  17. Article
  18. Article
  19. Restriction of innate Tγδ17 cell plasticity by an AP-1 regulatory axis.bioRxiv : the preprint server for biology · 2024
    Article
  20. Article
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

14 authors.

Minji LeeDivision of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
Eunmin LeeDepartment of New Biology, DGIST, Daegu, 42988, Republic of Korea.ORCID http://orcid.org/0000-0003-1793-6115
Seong Kyu HanDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
Yoon Ha ChoiDepartment of New Biology, DGIST, Daegu, 42988, Republic of Korea.
Dong-Il KwonDivision of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
Hyobeen ChoiDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.ORCID http://orcid.org/0000-0002-5007-0643
Kwanghwan LeeDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
Eun Seo ParkDepartment of New Biology, DGIST, Daegu, 42988, Republic of Korea.
Min-Seok RhaLaboratory of Immunology and Infectious Diseases, Graduate School of Medical Science and Engineering, KAIST, Daejeon, Korea.
Dong Jin JooDepartment of Surgery, Yonsei University, College of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0001-8405-1531
Eui-Cheol ShinLaboratory of Immunology and Infectious Diseases, Graduate School of Medical Science and Engineering, KAIST, Daejeon, Korea.
Sanguk KimDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea. sukim@postech.ac.kr.ORCID http://orcid.org/0000-0002-3449-3814
Jong Kyoung KimDepartment of New Biology, DGIST, Daegu, 42988, Republic of Korea. jkkim@dgist.ac.kr.ORCID http://orcid.org/0000-0002-0257-0547
You Jeong LeeDivision of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea. youjeong77@postech.ac.kr.ORCID http://orcid.org/0000-0002-6786-6955

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Invariant natural killer T (iNKT), mucosal-associated invariant T (MAIT), and γδ T cells are innate T cells that acquire memory phenotype in the thymus and share similar biological characteristics. However, how their effector differentiation is developmentally regulated is still unclear. Here, we identify analogous effector subsets of these three innate T cell types in the thymus that share transcriptional profiles. Using single-cell RNA sequencing, we show that iNKT, MAIT and γδ T cells mature via shared, branched differentiation rather than linear maturation or TCR-mediated instruction. Simultaneous TCR clonotyping analysis reveals that thymic maturation of all three types is accompanied by clonal selection and expansion. Analyses of mice deficient of TBET, GATA3 or RORγt and additional in vivo experiments corroborate the predicted differentiation paths, while human innate T cells from liver samples display similar features. Collectively, our data indicate that innate T cells share effector differentiation processes in the thymus.

Indexed as

Cell DifferentiationImmunity, InnateAnimalsCells, CulturedClonal Selection, Antigen-MediatedHumansLiverLymphocyte ActivationMiceMucosal-Associated Invariant T CellsNatural Killer T-CellsSequence Analysis, RNASingle-Cell AnalysisTh17 CellsThymus GlandT-Lymphocytes

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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.