Evidence map›Paper›PMID 30222143›Full record

ArticleJournal of visualized experiments : JoVE2018

Dynamic Proteomic and miRNA Analysis of Polysomes from Isolated Mouse Heart After Langendorff Perfusion.

Miroslava Stastna, Amandine Thomas, Juliana Germano, Somayeh Pourpirali, Jennifer E Van Eyk, Roberta A Gottlieb

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Decrease of Cardiac Parkin Protein in Obese Mice.Frontiers in cardiovascular medicine · 2019
    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

6 authors.

Miroslava StastnaThe Smidt Heart Institute, Cedars-Sinai Medical Center; Advanced Clinical Biosystems Research Institute, Cedars-Sinai Medical Center; Institute of Analytical Chemistry of the Czech Academy of Sciences.
Amandine ThomasThe Smidt Heart Institute, Cedars-Sinai Medical Center.
Juliana GermanoThe Smidt Heart Institute, Cedars-Sinai Medical Center.
Somayeh PourpiraliThe Smidt Heart Institute, Cedars-Sinai Medical Center.
Jennifer E Van EykThe Smidt Heart Institute, Cedars-Sinai Medical Center; Advanced Clinical Biosystems Research Institute, Cedars-Sinai Medical Center.
Roberta A GottliebThe Smidt Heart Institute, Cedars-Sinai Medical Center; Roberta.Gottlieb@cshs.org.

Funding

Genomic and Proteomic Architecture of AtherosclerosisR01HL111362 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HERRINGTON, DAVID MCLEOD · 2012 to 2021
$17.2M
Protein Chemistry and ProteomicsP01HL112730 · NHLBI · SAN DIEGO STATE UNIVERSITY · PI VAN EYK, JENNIFER E · 2013 to 2017
$12.0M
Mitochondrial Turnover in the Human HeartR01HL132075 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI GOTTLIEB, ROBERTA A., VAN EYK, JENNIFER E · 2017 to 2020
$2.1M
NHLBI NIH HHS P01 HL112730NHLBI NIH HHS R01 HL111362NHLBI NIH HHS R01 HL132075
6 · The paper itself

Abstract

Studies in dynamic changes in protein translation require specialized methods. Here we examined changes in newly-synthesized proteins in response to ischemia and reperfusion using the isolated perfused mouse heart coupled with polysome profiling. To further understand the dynamic changes in protein translation, we characterized the mRNAs that were loaded with cytosolic ribosomes (polyribosomes or polysomes) and also recovered mitochondrial polysomes and compared mRNA and protein distribution in the high-efficiency fractions (numerous ribosomes attached to mRNA), low-efficiency (fewer ribosomes attached) which also included mitochondrial polysomes, and the non-translating fractions. miRNAs can also associate with mRNAs that are being translated, thereby reducing the efficiency of translation, we examined the distribution of miRNAs across the fractions. The distribution of mRNAs, miRNAs, and proteins was examined under basal perfused conditions, at the end of 30 min of global no-flow ischemia, and after 30 min of reperfusion. Here we present the methods used to accomplish this analysis-in particular, the approach to optimization of protein extraction from the sucrose gradient, as this has not been described before-and provide some representative results.

Indexed as

AnimalsHeartMiceMicroRNAsPolyribosomesProteomicsRNA, MessengerMicroRNAsRNA, Messenger

Identifiers

PMID30222143
PMCPMC6231915

What OpenQuestion holds

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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.