Evidence map›Paper›PMID 31717790›Full record

ArticleMethods and protocols2019

High-Throughput Phenotyping Toolkit for Characterizing Cellular Models of Hypertrophic Cardiomyopathy In Vitro.

Diogo Mosqueira, Katarzyna Lis-Slimak, Chris Denning

Open access · goldAbstract read
In one paragraph

Article in Methods and protocols, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Cells · 2022
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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

3 authors at 1 institution in 1 country.

Diogo MosqueiraDepartment of Stem Cell Biology, Centre of Biomolecular Sciences, University of Nottingham, Nottingham NG7 2RD, UK.
Katarzyna Lis-SlimakDepartment of Stem Cell Biology, Centre of Biomolecular Sciences, University of Nottingham, Nottingham NG7 2RD, UK.ORCID 0000-0002-8997-544X
Chris DenningDepartment of Stem Cell Biology, Centre of Biomolecular Sciences, University of Nottingham, Nottingham NG7 2RD, UK.
University of Nottingham · GB

Funding

Britain Israel Research and Academic Exchange Partnership (BIRAX) 04BX14CDLGBritish Heart Foundation P47352/CRMBritish Heart Foundation PG/14/59/31000British Heart Foundation RG/14/1/30588British Heart Foundation RM/13/30157British Heart Foundation SP/15/9/31605Deutsche Forschungsgemeinschaft DFG-Es-88/12-1Deutsche Forschungsgemeinschaft HA3423/5-1Deutsches Zentrum für Herz-Kreislaufforschung N/AEngineering and Physical Sciences Research Council DM's Doctoral Prize Research FellowshipEuropean Commission FP7-BiodesignEuropean Research Council ERC-AG-IndivuHeartFreie und Hansestadt Hamburg N/AGerman Ministry of Education and Research N/AHeart Research UK N/AMedical Research Council MR/L012618/1Medical Research Council MR/M017354/1National Centre for the Replacement Refinement and Reduction of Animals in Research CRACK-IT:35911-259146National Centre for the Replacement Refinement and Reduction of Animals in Research NC/K000225/1National Centre for the Replacement Refinement and Reduction of Animals in Research NC/S001808/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/C013105/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/C013202/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/K000225/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/S001808/1
6 · The paper itself

Abstract

Hypertrophic cardiomyopathy (HCM) is a prevalent and complex cardiovascular disease characterised by multifarious hallmarks, a heterogeneous set of clinical manifestations, and several molecular mechanisms. Various disease models have been developed to study this condition, but they often show contradictory results, due to technical constraints and/or model limitations. Therefore, new tools are needed to better investigate pathological features in an unbiased and technically refined approach, towards improving understanding of disease progression. Herein, we describe three simple protocols to phenotype cellular models of HCM in vitro, in a high-throughput manner where technical artefacts are minimized. These are aimed at investigating: (1) Hypertrophy, by measuring cell volume by flow cytometry; (2) HCM molecular features, through the analysis of a hypertrophic marker, multinucleation, and sarcomeric disarray by high-content imaging; and (3) mitochondrial respiration and content via the Seahorse™ platform. Collectively, these protocols comprise straightforward tools to evaluate molecular and functional parameters of HCM phenotypes in cardiomyocytes in vitro. These facilitate greater understanding of HCM and high-throughput drug screening approaches and are accessible to all researchers of cardiac disease modelling. Whilst HCM is used as an exemplar, the approaches described are applicable to other cellular models where the investigation of identical biological changes is paramount.

Indexed as

cardiomyocytescellular modelsdisease modellingdrug screeninghigh-content imaginghigh-throughputhypertrophic cardiomyopathyhypertrophymitochondrial respirationphenotyping

Identifiers

PMID31717790
PMCPMC6961126
OpenAlexW2982274858

What OpenQuestion holds

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LicenceCC BY
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.