Evidence map›Paper›PMID 33597545›Full record

ArticleNature communications2021

Single-cell transcriptional profiling of human thymic stroma uncovers novel cellular heterogeneity in the thymic medulla.

Jhoanne L Bautista, Nathan T Cramer, Corey N Miller, Jessica Chavez, David I Berrios, Lauren E Byrnes, Joe Germino, Vasilis Ntranos, Julie B Sneddon, Trevor D Burt and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 129 papers.

0numbers the graph read from it
0cells of the map it votes in
129citing papers in PubMed
12.9field-weighted citation impact, top 1% 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

129 citing papers in PubMed, 185 citations in OpenAlex.

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  7. Runx3 instructs AireJournal of autoimmunity · 2026
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69 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 1 country.

Jhoanne L BautistaDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Nathan T CramerDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Corey N MillerDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Jessica ChavezDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
David I BerriosDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Lauren E ByrnesDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.ORCID 0000-0001-5991-8201
Joe GerminoDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.ORCID 0000-0003-3939-3342
Vasilis NtranosDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Julie B SneddonDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.ORCID 0000-0002-7404-8598
Trevor D BurtBroad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, CA, USA.ORCID 0000-0001-7933-529X
James M GardnerDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Chun J YeBakar Institute for Computational Health Sciences, University of California, San Francisco, San Francisco, CA, USA.ORCID 0000-0001-6560-3783
Mark S Anderson *Diabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Audrey V Parent *Diabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA. Audrey.Parent@ucsf.edu.ORCID 0000-0003-4506-6268
University of California, San Francisco · USDuke University · US

Funding

Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VAISSE, CHRISTIAN · 2003 to 2019
$21.8M
MOLECULAR AND CELLULAR IMMUNOLOGYT32AI007334 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CYSTER, JASON G · 1988 to 2023
$11.0M
RESOURCE-BASED CENTER FOR THE ADVANCEMENT OF PRECISION MEDICINE IN RHEUMATOLOGYP30AR070155 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Mary C Nakamura · 2016 to 2026
$8.2M
PREDOCTORAL TRAINING IN DEVELOPMENTAL BIOLOGYT32HD007470 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Todd Nystul · 1994 to 2026
$7.7M
Modeling autoimmune pathogenesis and beta cell destruction by T1D immune systemsU01DK123559 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ANDERSON, MARK S, PARENT, AUDREY · 2019 to 2023
$4.3M
Filling a Void of Research (FAVOR) Training for Transplant SurgeonsT32AI125222 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PETER G STOCK, Minnie M Sarwal · 2016 to 2026
$3.4M
Using human stem cell-derived thymic epithelium to remodel T1D immune toleranceU01DK107383 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ANDERSON, MARK S, BLUESTONE, JEFFREY A · 2016 to 2019
$2.3M
Defining Transition from Fetal to Adult T Cell Predominance in the Human FetusK08HD067295 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BURT, TREVOR DEON · 2011 to 2015
$628k
NIAID NIH HHS T32 AI007334NIAID NIH HHS T32 AI125222NIAMS NIH HHS P30 AR070155NICHD NIH HHS K08 HD067295NICHD NIH HHS T32 HD007470NIDDK NIH HHS P30 DK063720NIDDK NIH HHS U01 DK107383NIDDK NIH HHS U01 DK123559
6 · The paper itself

Abstract

The thymus' key function in the immune system is to provide the necessary environment for the development of diverse and self-tolerant T lymphocytes. While recent evidence suggests that the thymic stroma is comprised of more functionally distinct subpopulations than previously appreciated, the extent of this cellular heterogeneity in the human thymus is not well understood. Here we use single-cell RNA sequencing to comprehensively profile the human thymic stroma across multiple stages of life. Mesenchyme, pericytes and endothelial cells are identified as potential key regulators of thymic epithelial cell differentiation and thymocyte migration. In-depth analyses of epithelial cells reveal the presence of ionocytes as a medullary population, while the expression of tissue-specific antigens is mapped to different subsets of epithelial cells. This work thus provides important insight on how the diversity of thymic cells is established, and how this heterogeneity contributes to the induction of immune tolerance in humans.

Indexed as

Genetic HeterogeneityAdultAnimalsCell DifferentiationCell LineageEndothelial CellsEpithelial CellsGene Expression ProfilingHumansMesodermMicePericytesSingle-Cell AnalysisThymocytesThymus GlandT-Lymphocytes

Identifiers

PMID33597545
PMCPMC7889611
OpenAlexW3131547751

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.