Evidence map›Paper›PMID 8362975›Full record

ArticleThe American journal of pathology1993

Platelet activation releases megakaryocyte-synthesized apolipoprotein J, a highly abundant protein in atheromatous lesions.

D P Witte, B J Aronow, M L Stauderman, W D Stuart, M A Clay, R A Gruppo, S H Jenkins, J A Harmony

Open access · greenAbstract read
In one paragraph

Article in The American journal of pathology, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Early Prediction Model of Gestational Hypertension by Multi-Biomarkers Before 20 Weeks Gestation.Diabetes, metabolic syndrome and obesity : targets and therapy · 2021
    Article
  4. Distinct Proteomic Signatures in 16 HDL (High-Density Lipoprotein) Subspecies.Arteriosclerosis, thrombosis, and vascular biology · 2018
    Article
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  12. Prothrombin deficiency results in embryonic and neonatal lethality in mice.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  13. Article
  14. Article
  15. Plasminogen deficiency accelerates vessel wall disease in mice predisposed to atherosclerosis.Proceedings of the National Academy of Sciences of the United States of America · 1997
    Article
  16. Article
  17. Article
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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 1 institution in 1 country.

D P WitteDepartment of Pathology, Children's Hospital Medical Center, Cincinnati, OH 45229.
B J Aronow
M L Stauderman
W D Stuart
M A Clay
R A Gruppo
S H Jenkins
J A Harmony
Cincinnati Children's Hospital Medical Center · US

Funding

SPATIAL RELATIONSHIPS IN CARDIAC TROPONIN--ACIDOSIS AND PHOSPHORYLATIONP01HL041496 · NHLBI · UNIVERSITY OF CINCINNATI · PI ROBBINS, JEFFREY · 1988 to 2000
$2.6M
CELL BEHAVIOR: ROLE OF MEMBRANE-BOUND LIPOPROTEINSR01HL027333 · NHLBI · UNIVERSITY OF CINCINNATI · PI HARMONY, JUDITH A · 1985 to 1986
–
CELL BEHAVIOR: ROLE OF MEMBRANE-BOUND LIPOPROTEINSR37HL027333 · NHLBI · UNIVERSITY OF CINCINNATI · PI HARMONY, JUDITH A · 1987 to 1996
–
NHLBI NIH HHS HL27333NHLBI NIH HHS HL41496
6 · The paper itself

Abstract

Apolipoprotein J (apoJ) is an abundant glycoprotein in many biological fluids, and its constitutive high level synthesis is characteristic of many epithelial cells exposed to harsh fluids such as urine, bile, and gastric secretions. In addition, dramatic induction of apoJ occurs in cells surrounding several kinds of pathological lesions. Because platelets and circulating inflammatory cells represent critical elements in numerous pathological processes, we evaluated bone marrow cells for the presence of apoJ. Based upon messenger RNA in situ hybridization and immunofluorescent protein detection, high-level apoJ gene expression and protein accumulation occurred exclusively in mature megakaryocytes. Our results indicate that apoJ is stored in platelet granules and is released into extracellular fluid following platelet activation. Because atheromatous plaque development involves platelet aggregation and activation, we looked for and found abundant apoJ protein in advanced human atheromatous lesions. Thus, platelet sequestration and activation may lead to the rapid deployment of apoJ into sites of vascular injury. We hypothesize that platelet-derived apoJ participates in both short-term wound repair processes and chronic pathogenic processes at vascular interfaces.

Indexed as

Molecular ChaperonesAnimalsArteriosclerosisBlood PlateletsBone MarrowCell LineClusterinGlycoproteinsHumansImmunohistochemistryIn Situ HybridizationMegakaryocytesMiceMicroscopy, ImmunoelectronPlatelet ActivationRNA, MessengerCLU protein, humanClu protein, mouseClusterinGlycoproteinsMolecular ChaperonesRNA, Messenger

Identifiers

PMID8362975
PMCPMC1887200
OpenAlexW239434478

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.