Evidence map›Paper›PMID 22253476›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2012

Nonmuscle myosin IIA facilitates vesicle trafficking for MG53-mediated cell membrane repair.

Peihui Lin, Hua Zhu, Chuanxi Cai, Xianhua Wang, Chunmei Cao, Ruiping Xiao, Zui Pan, Noah Weisleder, Hiroshi Takeshima, Jianjie Ma

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

54 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Cardiomyocyte damage control in heart failure and the role of the sarcolemma.Journal of muscle research and cell motility · 2019
    Article
  20. Article
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

10 authors at 4 institutions in 4 countries.

Peihui LinDepartment of Physiology and Biophysics, Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.
Hua Zhu
Chuanxi Cai
Xianhua Wang
Chunmei Cao
Ruiping Xiao
Zui Pan
Noah Weisleder
Hiroshi Takeshima
Jianjie Ma
Johnson University · USInstitute of Molecular Medicine · INKing University · USKyoto Pharmaceutical University · JP

Funding

Modulation of MG53 Function in Cardiac Membrane RepairR01HL069000 · NHLBI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI MA, JIANJIE · 2002 to 2016
$5.3M
MG53-Mediated Membrane Repair in Muscle Physiology and DiseaseR01AR061385 · NIAMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI LIN, PEI-HUI · 2011 to 2020
$3.8M
Enhancing the effectiveness of human cardiac stem cell therapyR01HL114951 · NHLBI · UNIVERSITY OF LOUISVILLE · PI CAI, CHUANXI · 2012 to 2016
$1.9M
MG53 mediated myocardial repair for ischemic heart diseaseR21HL104315 · NHLBI · UNIVERSITY OF LOUISVILLE · PI CAI, CHUANXI · 2010 to 2011
$410k
NHLBI NIH HHS R01 HL069000NHLBI NIH HHS R01-HL069000NHLBI NIH HHS R01 HL114951NHLBI NIH HHS R21 HL104315NIAMS NIH HHS R01 AR061385NIAMS NIH HHS R01-AR061385
6 · The paper itself

Abstract

Repair of injury to the plasma membrane is an essential mechanism for maintenance of cellular homeostasis and integrity that involves coordinated movement of intracellular vesicles to membrane injury sites to facilitate patch formation. We have previously identified MG53 as an essential component of the cell membrane repair machinery. In order for MG53 and intracellular vesicles to translocate to membrane injury sites, motor proteins must be involved. Here, we show that nonmuscle myosin type IIA (NM-IIA) interacts with MG53 to regulate vesicle trafficking during cell membrane repair. In cells that are deficient for NM-IIA expression, MG53 cannot translocate to acute injury sites, whereas rescue of NM-IIA expression in these cells can restore MG53-mediated membrane repair. Compromised cell membrane repair is observed in cells with RNAi-mediated knockdown of NM-IIA expression, or following pharmacological alteration of NM-IIA motor function. Together, our data reveal NM-IIA as a key cytoskeleton motor protein that facilitates vesicle trafficking during MG53-mediated cell membrane repair.

Indexed as

Amino Acid SequenceAnimalsCarrier ProteinsCell LineCell MembraneChlorocebus aethiopsCOS CellsDNA PrimersHumansMolecular Sequence DataNonmuscle Myosin Type IIAProtein TransportRNA InterferenceTripartite Motif ProteinsCarrier ProteinsDNA PrimersNonmuscle Myosin Type IIATRIM72 protein, humanTripartite Motif Proteins

Identifiers

PMID22253476
PMCPMC3336789
OpenAlexW2120822929

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.