Evidence map›Paper›PMID 21454454›Full record

ArticleBlood2011

Regulatory effects of TLR2 on megakaryocytic cell function.

Lea M Beaulieu, Elaine Lin, Kristine M Morin, Kahraman Tanriverdi, Jane E Freedman

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

59 citing papers in PubMed, 106 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Towards liquid biopsy-based analysis of antitumour immunity.Nature reviews. Clinical oncology · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Immunological face of megakaryocytes.Frontiers of medicine · 2024
    Review
  10. Article
  11. Versatility of megakaryocytes in homeostasis and disease.Blood science (Baltimore, Md.) · 2024
    Review
  12. Article
  13. Megakaryocytes in the lung: History and future perspectives.Research and practice in thrombosis and haemostasis · 2023
    Article
  14. Review
  15. Toll-like Receptors and Thrombopoiesis.International journal of molecular sciences · 2023
    Review
  16. Article
  17. Article
  18. Article
  19. CXCR4eLife · 2022
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Lea M BeaulieuWhitaker Cardiovascular Institute, Department of Medicine, Boston University School of Medicine, 700 Albany Street, Boston, MA 02118, USA. lmb@bu.edu
Elaine Lin
Kristine M Morin
Kahraman Tanriverdi
Jane E Freedman
Boston University · US

Funding

Multidisciplinary Training in Cardiovascular ResearchT32HL007224 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI HAMBURG, NAOMI MIRIAM, WAINFORD, RICHARD DAVID · 1985 to 2020
$12.3M
Vascular Consequences of Insulin Resistance and ObesityP50HL083801 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI VITA, JOSEPH A. · 2006 to 2010
$11.2M
Role of Innate Immune System in Pathogen Induced Chronic InflammationP01AI078894 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GENCO, CAROLINE A · 2010 to 2014
$7.4M
NHLBI NIH HHS P01 HL083801NHLBI NIH HHS P50 HL083801NHLBI NIH HHS T32 HL007224NHLBI NIH HHS T32 HL07224NIAID NIH HHS P01 AI078894
6 · The paper itself

Abstract

TLR2, a functional, inflammatory-related receptor, is known to be expressed on megakaryocytes and platelets and to lead to infection and immune-mediated activation of platelets; however, the role of this receptor in megakaryocytes is not understood. Using Meg-01 cells and mouse megakaryocytes, we found that NFκB, ERK-MAPK, and PI3K/Akt pathways, known downstream pathways of TLRs, are activated by Pam3CSK4, a TLR2-specific ligand. In addition, transcription factors associated with megakaryocyte maturation, GATA-1, NF-E2, and mammalian target of rapamycin (mTOR), are all increased in the presence of Pam3CSK4. The effect of Pam3CSK4 on megakaryocyte maturation was verified by the increase in DNA content and adhesion to extracellular matrix proteins by TLR2-dependent stimulation. In addition, TLR2 stimulation resulted in an increase in reactive oxygen species (ROS) production. Gene expression and protein levels of GP1b, CD41, MCP-1, COX2, NFκB1, and TLR2 were up-regulated in megakaryocytes after TLR2 stimulation through NFκB, PI3K/Akt, and ERK-MAPK pathways. Treatment of wild-type mice with Pam3CSK4 resulted in a return to normal platelet levels and an increase in megakaryocyte maturation, which did not occur in the TLR2(-/-) mice. Therefore, inflammation, through TLR2, can increase maturation and modulate the phenotype of megakaryocytes, contributing to the interrelationship between inflammation and hemostasis.

Indexed as

AnimalsBlotting, WesternCell AdhesionCells, CulturedEnzyme-Linked Immunosorbent AssayFlow CytometryMegakaryocytesMiceMice, Inbred C57BLMice, KnockoutMitogen-Activated Protein Kinase 3NF-kappa BPhosphatidylinositol 3-KinasesPlatelet ActivationPloidiesProto-Oncogene Proteins c-aktMitogen-Activated Protein Kinase 3NF-kappa BPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReactive Oxygen SpeciesRNA, MessengerTlr2 protein, mouseToll-Like Receptor 2

Identifiers

PMID21454454
PMCPMC3112041
OpenAlexW1989739445

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.