Evidence map›Paper›PMID 18802008›Full record

ArticleBlood2009

Megakaryocyte-derived microparticles: direct visualization and distinction from platelet-derived microparticles.

Robert Flaumenhaft, James R Dilks, Jennifer Richardson, Eva Alden, Sunita R Patel-Hett, Elisabeth Battinelli, Giannoula L Klement, Martha Sola-Visner, Joseph E Italiano

Open access · greenAbstract read
In one paragraph

Article in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 154 papers.

0numbers the graph read from it
0cells of the map it votes in
154citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

154 citing papers in PubMed, 314 citations in OpenAlex.

  1. Review
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  10. Article
  11. Circulating Extracellular Vesicles in Cardiovascular Disease.International journal of molecular sciences · 2025
    Review
  12. Review
  13. Observational
  14. Article
  15. Review
  16. Article
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  18. Article
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94 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Robert FlaumenhaftDivision of Hemostasis and Thrombosis, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA. rflaumen@bidmc.harvard.edu
James R Dilks
Jennifer Richardson
Eva Alden
Sunita R Patel-Hett
Elisabeth Battinelli
Giannoula L Klement
Martha Sola-Visner
Joseph E Italiano
Boston Children's Hospital · USBrigham and Women's Hospital · USBeth Israel Deaconess Medical Center · USDana-Farber Cancer Institute · US

Funding

Cytoskeletal Mechanisms of Platelet FormationR01HL068130 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI ITALIANO, JOSEPH E · 2001 to 2021
$8.1M
Prolonged and Severe Thrombocytopenia in NeonatesR01HL069990 · NHLBI · UNIVERSITY OF FLORIDA · PI SOLA-VISNER, MARTHA C. · 2002 to 2015
$2.8M
SNARE PROTEINS IN PLATELET ALPHA-GRANULE SECRETIONR01HL063250 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI FLAUMENHAFT, ROBERT C · 2000 to 2007
$2.5M
NHLBI NIH HHS HL63250NHLBI NIH HHS HL68130NHLBI NIH HHS R01 HL063250NHLBI NIH HHS R01 HL068130NHLBI NIH HHS R01 HL069990
6 · The paper itself

Abstract

Platelet microparticles are a normal constituent of circulating blood. Several studies have demonstrated positive correlations between thrombotic states and platelet microparticle levels. Yet little is known about the processes by which platelet microparticles are generated in vivo. We now characterize microparticles derived directly from megakaryocytes. Video microscopy of live mouse megakaryocytes demonstrated that microparticles form as submicron beads along the lengths of slender, unbranched micropodia. These microparticles are CD41(+), CD42b(+), and express surface phosphatidylserine. Megakaryocyte microparticle generation is resistant to inhibition of microtubule assembly, which is critical to platelet formation, and augmented by inhibition of actin polymerization. To determine whether circulating microparticles are derived primarily from activated platelets or megakaryocytes, we identified markers that distinguish between these 2 populations. CD62P and LAMP-1 were found only on mouse microparticles from activated platelets. In contrast, full-length filamin A was found in megakaryocyte-derived microparticles, but not microparticles from activated platelets. Circulating microparticles isolated from mice were CD62P(-), LAMP-1(-) and expressed full-length filamin A, indicating a megakaryocytic origin. Similarly, circulating microparticles isolated from healthy volunteers were CD62P(-) and expressed full-length filamin A. Cultured human megakaryocytes elaborated microparticles that were CD41(+), CD42b(+), and express surface phosphatidylserine. These results indicate that direct production by megakaryocytes represents a physiologic means to generate circulating platelet microparticles.

Indexed as

ActinsAnimalsBlood PlateletsCell-Derived MicroparticlesCells, CulturedContractile ProteinsFilaminsHumansLysosomal-Associated Membrane Protein 1Lysosomal Membrane ProteinsMegakaryocytesMiceMicrofilament ProteinsMicrotubulesPhosphatidylserinesPlatelet Glycoprotein GPIb-IX ComplexActinsContractile ProteinsFilaminsLAMP1 protein, humanLamp1 protein, mouseLysosomal-Associated Membrane Protein 1Lysosomal Membrane ProteinsMicrofilament ProteinsPhosphatidylserinesPlatelet Glycoprotein GPIb-IX ComplexPlatelet Membrane Glycoprotein IIbP-Selectin

Identifiers

PMID18802008
PMCPMC2635076
OpenAlexW2015445251

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.