Evidence map›Paper›PMID 24458007›Full record

ArticleAutophagy2014

Dissection of autophagy in human platelets.

Wenfeng Feng, Chunmei Chang, Dongjiao Luo, Hua Su, Shanshan Yu, Wen Hua, Zhihua Chen, Hu Hu, Wei Liu

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

62 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Redox Control in Platelet Activity and Therapy.Antioxidants (Basel, Switzerland) · 2025
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. High Autophagy Patterns in Swelling Platelets During Apheresis Platelet Storage.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2023
    Article

2 more citing papers are in PubMed but not listed here.

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

9 authors at 2 institutions in 3 countries.

Wenfeng FengDepartment of Biochemistry and Molecular Biology; Program in Molecular and Cell Biology; Zhejiang University School of Medicine; Hangzhou, China.
Chunmei ChangDepartment of Biochemistry and Molecular Biology; Program in Molecular and Cell Biology; Zhejiang University School of Medicine; Hangzhou, China.
Dongjiao LuoDepartment of Pathology and Pathophysiology; Zhejiang University School of Medicine; Hangzhou, China.
Hua SuDepartment of Biochemistry and Molecular Biology; Program in Molecular and Cell Biology; Zhejiang University School of Medicine; Hangzhou, China.
Shanshan YuDepartment of Pathology and Pathophysiology; Zhejiang University School of Medicine; Hangzhou, China.
Wen HuaDepartment of Respiratory Medicine; Second Affiliated Hospital; Zhejiang University School of Medicine; Hangzhou, China.
Zhihua ChenDepartment of Respiratory Medicine; Second Affiliated Hospital; Zhejiang University School of Medicine; Hangzhou, China.
Hu HuDepartment of Pathology and Pathophysiology; Zhejiang University School of Medicine; Hangzhou, China.
Wei LiuDepartment of Biochemistry and Molecular Biology; Program in Molecular and Cell Biology; Zhejiang University School of Medicine; Hangzhou, China; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Disease; First Affiliated Hospital; Zhejiang University School of Medicine; Hangzhou, China.
Zhejiang University · CNInstitute of Molecular and Cell Biology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Continuous turnover of intracellular components by autophagy is necessary to preserve cellular homeostasis in all tissues. Despite recent advances in identifying autophagy-related genes and understanding the functions of autophagy in developmental and pathological conditions, so far, the role of autophagy in platelet, a specific anucleate cell type, is poorly understood. In this study, we showed that human platelets express the autophagy-related proteins ATG5, ATG7, and LC3. The same as in nucleated mammalian cells, autophagy was stimulated by cell starvation or the MTOR inhibitor rapamycin in a phosphatidylinositol 3-kinase (PtdIns3K)-dependent manner. Disruption of autophagic flux led to impairment of platelet aggregation and adhesion. Furthermore, Becn1 heterozygous knockout mice displayed a prolonged bleeding time and reduced platelet aggregation. These results suggest a potential role of autophagy in the regulation of platelet function, and imply that gene transcription may not be an essential prerequisite for adaptive autophagy.

Indexed as

AnimalsApoptosis Regulatory ProteinsAutophagyBeclin-1Bleeding TimeBlood PlateletsHeterozygoteHumansMicePhosphatidylinositol 3-KinasesSignal TransductionTOR Serine-Threonine KinasesTranscriptional ActivationApoptosis Regulatory ProteinsBeclin-1Becn1 protein, mousePhosphatidylinositol 3-KinasesTOR Serine-Threonine KinasesautophagosomeautophagyBeclin 1plateletthrombus

Identifiers

PMID24458007
PMCPMC4091151
OpenAlexW2033085746

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.