Evidence map›Paper›PMID 22362037›Full record

ArticleBlood2012

Regulation of mast cell survival and function by tuberous sclerosis complex 1.

Jinwook Shin, Hongjie Pan, Xiao-Ping Zhong

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Role of TSC1 in physiology and diseases.Molecular and cellular biochemistry · 2021
    Review
  5. Article
  6. Article
  7. Article
  8. Essential Role of mTORC1 in Self-Renewal of Murine Alveolar Macrophages.Journal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Regulation of innate immune cell function by mTOR.Nature reviews. Immunology · 2015
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Mechanistic target of rapamycin complex 1 is critical for invariant natural killer T-cell development and effector function.Proceedings of the National Academy of Sciences of the United States of America · 2014
    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

3 authors at 1 institution in 1 country.

Jinwook ShinDepartment of Pediatrics-Division of Allergy and Immunology, Duke University Medical Center, Durham, NC 27710, USA.
Hongjie Pan
Xiao-Ping Zhong
Duke Medical Center · US

Funding

Regulation of peripheral T cell toleranceR01AI079088 · NIAID · DUKE UNIVERSITY · PI ZHONG, XIAOPING · 2008 to 2019
$3.5M
A Murine Model of Chronic Autoimmune Hepatitis and Liver FibrosisR01AI076357 · NIAID · DUKE UNIVERSITY · PI ZHONG, XIAOPING · 2008 to 2012
$1.5M
Immunotherapy for Peanut AllergyR21AI079873 · NIAID · DUKE UNIVERSITY · PI ZHONG, XIAOPING · 2008 to 2009
$422k
NIAID NIH HHS R01 AI076357NIAID NIH HHS R01AI076357NIAID NIH HHS R01 AI079088NIAID NIH HHS R01AI079088NIAID NIH HHS R21 AI079873NIAID NIH HHS R21AI079873
6 · The paper itself

Abstract

Mast cells play critical roles in allergic disorders and asthma. The importance of tuberous sclerosis complex 1/2-mammalian target of rapamycin (TSC1/2-mTOR) signaling in mast cells is unknown. Here, we report that TSC1 is a critical regulator for mTOR signaling in mast cells downstream of FcεRI and c-Kit, and differentially controls mast cell degranulation and cytokine production. TSC1-deficiency results in impaired mast cell degranulation, but enhanced cytokine production in vitro and in vivo after FcεRI engagement. Furthermore, TSC1 is critical for mast cell survival through multiple pathways of apoptosis including the down-regulation of p53, miR-34a, reactive oxygen species, and the up-regulation of Bcl-2. Together, these findings reveal that TSC1 is a critical regulator of mast cell activation and survival, suggesting the manipulation of the TSC1/2-mTOR pathway as a therapeutic strategy for mast cell-mediated diseases.

Indexed as

AnimalsApoptosisCell DeathCell DegranulationCell LineCell SurvivalCytokinesGene ExpressionHumansImmunoglobulin EIntracellular Signaling Peptides and ProteinsMast CellsMechanistic Target of Rapamycin Complex 1MiceMice, TransgenicMicroRNAsCrtc2 protein, mouseCytokinesFcRI protein, mouseImmunoglobulin EIntracellular Signaling Peptides and ProteinsMechanistic Target of Rapamycin Complex 1MicroRNAsMIRN34a microRNA, mouseMultiprotein ComplexesProteinsProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-bcl-2Reactive Oxygen SpeciesTOR Serine-Threonine KinasesTrans-ActivatorsTranscription FactorsTSC1 protein, humanTsc1 protein, mouseTuberous Sclerosis Complex 1 ProteinTumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID22362037
PMCPMC3321856
OpenAlexW1990524611

What OpenQuestion holds

Textmetadata
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.