Evidence map›Paper›PMID 27233961›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

mTORC2 in Thymic Epithelial Cells Controls Thymopoiesis and T Cell Development.

Hong-Xia Wang, Joyce S Cheng, Shuai Chu, Yu-Rong Qiu, Xiao-Ping Zhong

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. 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
1.0field-weighted citation impact, top 22% 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, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Metabolic regulation of T cell development.Frontiers in immunology · 2022
    Review
  4. Article
  5. Review
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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 2 institutions in 2 countries.

Hong-Xia WangLaboratory Medicine Center, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, China; Division of Allergy and Immunology, Department of Pediatrics, Duke University Medical Center, Durham, NC 27710;
Joyce S ChengDivision of Allergy and Immunology, Department of Pediatrics, Duke University Medical Center, Durham, NC 27710; Pre-Med (BS/MD) Health Scholar Program, Temple University, Philadelphia, PA 19222;
Shuai ChuLaboratory Medicine Center, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, China; Division of Allergy and Immunology, Department of Pediatrics, Duke University Medical Center, Durham, NC 27710;ORCID 0000-0002-2164-2016
Yu-Rong QiuLaboratory Medicine Center, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, China; xiaoping.zhong@duke.edu qiuyuronggz@126.com.
Xiao-Ping ZhongDivision of Allergy and Immunology, Department of Pediatrics, Duke University Medical Center, Durham, NC 27710; Department of Immunology, Duke University Medical Center, Durham, NC 27710; and Hematologic Malignancies and Cellular Therapies Program, Duke Cancer Institute, Duke University Medical Center, Durham, NC 27710 xiaoping.zhong@duke.edu qiuyuronggz@126.com.ORCID 0000-0002-4619-8783
Nanfang Hospital · CNDuke Medical Center · US

Funding

Regulation of peripheral T cell toleranceR01AI079088 · NIAID · DUKE UNIVERSITY · PI ZHONG, XIAOPING · 2008 to 2019
$3.5M
TSC1-mTOR signaling and T cell toleranceR01AI101206 · NIAID · DUKE UNIVERSITY · PI ZHONG, XIAOPING · 2012 to 2016
$1.9M
NIAID NIH HHS R01 AI079088NIAID NIH HHS R01 AI101206
6 · The paper itself

Abstract

Thymic epithelial cells (TECs) play important roles in T cell generation. Mechanisms that control TEC development and function are still not well defined. The mammalian or mechanistic target of rapamycin complex (mTORC)2 signals to regulate cell survival, nutrient uptake, and metabolism. We report in the present study that mice with TEC-specific ablation of Rictor, a critical and unique adaptor molecule in mTORC2, display thymic atrophy, which accompanies decreased TEC numbers in the medulla. Moreover, generation of multiple T cell lineages, including conventional TCRαβ T cells, regulatory T cells, invariant NKT cells, and TCRγδ T cells, was reduced in TEC-specific Rictor-deficient mice. Our data demonstrate that mTORC2 in TECs is important for normal thymopoiesis and efficient T cell generation.

Indexed as

LymphopoiesisAnimalsCarrier ProteinsCell DifferentiationCell LineageCells, CulturedEpithelial CellsKiller Cells, NaturalLymphocyte SubsetsMechanistic Target of Rapamycin Complex 2MiceMice, Inbred C57BLMice, KnockoutMultiprotein ComplexesRapamycin-Insensitive Companion of mTOR ProteinReceptors, Antigen, T-Cell, alpha-betaCarrier ProteinsMechanistic Target of Rapamycin Complex 2Multiprotein ComplexesRapamycin-Insensitive Companion of mTOR ProteinReceptors, Antigen, T-Cell, alpha-betaReceptors, Antigen, T-Cell, gamma-deltarictor protein, mouseTOR Serine-Threonine Kinases

Identifiers

PMID27233961
PMCPMC4912958
OpenAlexW2394759216

What OpenQuestion holds

Textmetadata
LicenceTDM
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.