Evidence map›Paper›PMID 19088189›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2008

Regulation of lymphocyte progenitor survival by the proapoptotic activities of Bim and Bid.

Malay Mandal, Kelly M Crusio, Fanyong Meng, Suqing Liu, Marcus Kinsella, Marcus R Clark, Osamu Takeuchi, Iannis Aifantis

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Diverse Roles of Akt in T cells.Immunometabolism · 2021
    Article
  7. Article
  8. Article
  9. Review
  10. Transcription factors and target genes of pre-TCR signaling.Cellular and molecular life sciences : CMLS · 2015
    Review
  11. Article
  12. Review
  13. Rejuvenating Bi(d)ology.Oncogene · 2013
    Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. 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

8 authors at 3 institutions in 2 countries.

Malay MandalDepartment of Medicine, University of Chicago, Chicago, IL 60637, USA.
Kelly M Crusio
Fanyong Meng
Suqing Liu
Marcus Kinsella
Marcus R Clark
Osamu Takeuchi
Iannis Aifantis
University of Chicago · USNew York University · USOsaka University · JP

Funding

TRAINING PROGRAM IN MOLECULAR ONCOLOGY &IMMUNOLOGYT32CA009161 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CARROLL, WILLIAM L., LEVY, DAVID E · 1985 to 2020
$13.3M
Regulation of hematopoietic stem cell differentiationR01CA105129 · NCI · UNIVERSITY OF CHICAGO · PI AIFANTIS, IANNIS · 2005 to 2014
$2.8M
NCI NIH HHS 5 T32 CA 009161NCI NIH HHS R01 CA105129NCI NIH HHS R01CA105129NCI NIH HHS T32 CA009161
6 · The paper itself

Abstract

On their entry into the thymus, developing lymphocyte progenitors depend on signaling from the pre-T cell receptor (pre-TCR), which orchestrates differentiation, cell proliferation, and survival. The exact mechanism of pre-TCR-mediated suppression of T cell death remains unclear and controversial. Here, we identify Bim and Bid, 2 members of the BH3-only group of the BCL2 family, as important regulators of pre-T cell death. Both factors are highly expressed in proapoptotic thymocytes and their expression is suppressed on signaling through the pre-TCR. Their expression is directly regulated by the transcription factors FoxO3a and p53. Bid expression and p53 activity are related to the ongoing rearrangement of the TCR loci and induced DNA damage responses. Bim expression and FoxO3a nuclear translocation are directly controlled by the pre-TCR by means of its downstream kinase Akt/PKB. Interestingly, deletion of either gene on a pre-TCR(-/-) background rescues survival, but fails to induce further progenitor differentiation uncoupling the 2 processes.

Indexed as

Active Transport, Cell NucleusAnimalsApoptosis Regulatory ProteinsBcl-2-Like Protein 11BH3 Interacting Domain Death Agonist ProteinCell DeathCell DifferentiationCell NucleusCell ProliferationCell SurvivalDNA DamageForkhead Box Protein O3Forkhead Transcription FactorsGene Rearrangement, T-LymphocyteLymphoid Progenitor CellsMembrane ProteinsApoptosis Regulatory ProteinsBcl2l11 protein, mouseBcl-2-Like Protein 11BH3 Interacting Domain Death Agonist ProteinBid protein, mouseForkhead Box Protein O3Forkhead Transcription FactorsFoxO3 protein, mouseMembrane ProteinsProto-Oncogene ProteinsProto-Oncogene Proteins c-aktReceptors, Antigen, T-CellTumor Suppressor Protein p53

Identifiers

PMID19088189
PMCPMC2634950
OpenAlexW2153780013

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.