Evidence map›Paper›PMID 24106272›Full record

ArticleThe Journal of biological chemistry2013

Early growth response-1 (EGR-1) and nuclear factor of activated T cells (NFAT) cooperate to mediate CD40L expression in megakaryocytes and platelets.

Scott A Crist, Bennett D Elzey, Michelle T Ahmann, Timothy L Ratliff

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

21 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Immunological face of megakaryocytes.Frontiers of medicine · 2024
    Review
  4. Article
  5. Article
  6. Review
  7. Megakaryocytes in the lung: History and future perspectives.Research and practice in thrombosis and haemostasis · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. New Insights Into the Differentiation of Megakaryocytes From Hematopoietic Progenitors.Arteriosclerosis, thrombosis, and vascular biology · 2019
    Review
  16. Megakaryocytes as immune cells.Journal of leukocyte biology · 2019
    Review
  17. Article
  18. Article
  19. Article
  20. 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

4 authors at 2 institutions in 1 country.

Scott A CristDepartment of Comparative Pathobiology, Purdue University School of Veterinary Medicine, West Lafayette, Indiana 47907; Purdue Center for Cancer Research, Purdue University, West Lafayette, Indiana 47907.
Bennett D ElzeyDepartment of Comparative Pathobiology, Purdue University School of Veterinary Medicine, West Lafayette, Indiana 47907; Purdue Center for Cancer Research, Purdue University, West Lafayette, Indiana 47907.
Michelle T AhmannDepartment of Comparative Pathobiology, Purdue University School of Veterinary Medicine, West Lafayette, Indiana 47907.
Timothy L RatliffDepartment of Comparative Pathobiology, Purdue University School of Veterinary Medicine, West Lafayette, Indiana 47907; Purdue Center for Cancer Research, Purdue University, West Lafayette, Indiana 47907. Electronic address: scrist@purdue.edu.
Purdue University West Lafayette · USCenter for Cancer Research · US

Funding

Platelet Contribution to Thymus-dependent B cell ImmunityK01DK071712 · NIDDK · UNIVERSITY OF IOWA · PI ELZEY, BENNETT DAVID · 2006 to 2008
$381k
NIAID NIH HHS R01-AI06924NIDDK NIH HHS K01 DK071712
6 · The paper itself

Abstract

Increasing evidence implicates circulating platelets as mediators of chronic inflammatory and autoimmune diseases via the expression and release of CD40L, an important modulator of inflammation and adaptive immune responses traditionally associated with activated T cells. Emerging evidence suggests that platelet CD40L is dynamically regulated in several chronic inflammatory and autoimmune diseases and may mediate progression and secondary pathology associated with those disease states. The present study identifies NFATc2 as a key transcriptional modulator of CD40L expression in megakaryocytes and inflammatory activity of platelets. Furthermore, the current data show that EGR-1, a member of the early growth response family of zinc finger transcription factors, modulates NFATc2-dependent regulation of CD40L expression in megakaryocytes. Our novel demonstration that in vivo biochemical or genetic inhibition of NFATc2 activity in megakaryocyte diminishes platelet CD40L implicates the NFATc2/EGR-1 axis as a key regulatory pathway of inflammatory and immunomodulatory activity in platelets and represents a target for the development of therapeutics for the potential treatment of chronic inflammatory and autoimmune diseases.

Indexed as

AnimalsAutoimmune DiseasesBlood PlateletsCD40 LigandEarly Growth Response Protein 1Gene Expression RegulationHumansInflammationJurkat CellsK562 CellsMegakaryocytesMiceMice, Inbred BALB CMice, KnockoutNFATC Transcription FactorsCD40 LigandEarly Growth Response Protein 1EGR1 protein, humanEgr1 protein, mouseNFATC2 protein, humanNfatc2 protein, mouseNFATC Transcription FactorsEndothelial CellInflammationMegakaryocytesPlateletsSignalingTranscription

Identifiers

PMID24106272
PMCPMC3837138
OpenAlexW2069373300

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.