Evidence map›Paper›PMID 24340075›Full record

ArticlePloS one2013

Label retention identifies a multipotent mesenchymal stem cell-like population in the postnatal thymus.

Masako Osada, Varan J Singh, Kenmin Wu, Derek B Sant'Angelo, Mark Pezzano

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Twenty Years of AIRE.Frontiers in immunology · 2018
    Review
  6. Review
  7. Article
  8. Cutting to the chase: taking the pulse of label-retaining cells in kidney.American journal of physiology. Renal physiology · 2015
    Article
  9. Article
  10. Review
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 2 institutions in 1 country.

Masako OsadaDepartment of Biology, The City College of New York, CUNY, New York, New York, United States of America.
Varan J Singh
Kenmin Wu
Derek B Sant'Angelo
Mark Pezzano
City College of New York · USRutgers, The State University of New Jersey · US

Funding

Training and Career Development and Education CoreU54CA137788 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Daniel Alan Heller · 2008 to 2026
$28.1M
TNC FUNCTION IN APOPTOTIC ANTIGEN DRIVEN AUTOIMMUNITYG12RR003060 · NCRR · CITY COLLEGE OF NEW YORK · PI WALLMAN, JOSHUA · 1985 to 2011
$26.1M
Cellular/Molecular Basis of Development: Research CenterG12MD007603 · NIMHD · CITY COLLEGE OF NEW YORK · PI PEZZANO, MARK · 2012 to 2017
$11.5M
Immunobiology of NKT cell development and functionR01AI059739 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI SANT'ANGELO, DEREK B. · 2006 to 2010
$2.5M
The function of PLZF in innate T cellsR01AI083988 · NIAID · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI SANT'ANGELO, DEREK B. · 2010 to 2014
$2.2M
Development and Maintenance of Thymic Epithelial MicroenvironmentsSC1AI104994 · NIAID · CITY COLLEGE OF NEW YORK · PI PEZZANO, MARK · 2012 to 2015
$1.4M
Crosstalk Control of Thymic Epithelial DevelopmentSC1AI081527 · NIAID · CITY COLLEGE OF NEW YORK · PI PEZZANO, MARK · 2008 to 2011
$1.1M
NCI NIH HHS 1U54CA137788NCI NIH HHS U54 CA137788NCRR NIH HHS 2G12RR03060-26A1NCRR NIH HHS G12 RR003060NIAID NIH HHS 1SC1AI081527NIAID NIH HHS 9SC1AI104994NIAID NIH HHS AI059739NIAID NIH HHS R01 AI059739NIAID NIH HHS R01 AI083988NIAID NIH HHS SC1 AI081527NIAID NIH HHS SC1 AI104994NIMHD NIH HHS 8G12MD007603-27NIMHD NIH HHS G12 MD007603
6 · The paper itself

Abstract

Thymic microenvironments are essential for the proper development and selection of T cells critical for a functional and self-tolerant adaptive immune response. While significant turnover occurs, it is unclear whether populations of adult stem cells contribute to the maintenance of postnatal thymic epithelial microenvironments. Here, the slow cycling characteristic of stem cells and their property of label-retention were used to identify a K5-expressing thymic stromal cell population capable of generating clonal cell lines that retain the capacity to differentiate into a number of mesenchymal lineages including adipocytes, chondrocytes and osteoblasts suggesting a mesenchymal stem cell-like phenotype. Using cell surface analysis both culture expanded LRCs and clonal thymic mesenchymal cell lines were found to express Sca1, PDGFRα, PDGFRβ,CD29, CD44, CD49F, and CD90 similar to MSCs. Sorted GFP-expressing stroma, that give rise to TMSC lines, contribute to thymic architecture when reaggregated with fetal stroma and transplanted under the kidney capsule of nude mice. Together these results show that the postnatal thymus contains a population of mesenchymal stem cells that can be maintained in culture and suggests they may contribute to the maintenance of functional thymic microenvironments.

Indexed as

AnimalsAntigens, LyBase SequenceCell DifferentiationCell LineageCell TransplantationFemaleGreen Fluorescent ProteinsHyaluronan ReceptorsIntegrin alpha6Integrin beta1KidneyMaleMesenchymal Stem CellsMiceMice, Inbred C57BLAntigens, LyCd44 protein, mouseGreen Fluorescent ProteinsHyaluronan ReceptorsIntegrin alpha6Integrin beta1Ly6 protein, mouseReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor betaThy-1 Antigens

Identifiers

PMID24340075
PMCPMC3858364
OpenAlexW2067478318

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.