Evidence map›Paper›PMID 28042345›Full record

ArticleCellular and molecular bioengineering2016

Biomimetic microstructure morphology in electrospun fiber mats is critical for maintaining healthy cardiomyocyte phenotype.

Rutwik Rath, Jung Bok Lee, Truc-Linh Tran, Sean F Lenihan, Cristi L Galindo, Yan Ru Su, Tarek Absi, Leon M Bellan, Douglas B Sawyer, Hak-Joon Sung

Abstract read
In one paragraph

Article in Cellular and molecular bioengineering, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Naturally Engineered Maturation of Cardiomyocytes.Frontiers in cell and developmental biology · 2017
    Review
  5. Review
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 1 institution in 1 country.

Rutwik RathDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN.
Jung Bok LeeDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN.
Truc-Linh TranDepartment of Medicine, Cardiovascular Division, Vanderbilt University, Nashville, TN.
Sean F LenihanDepartment of Medicine, Cardiovascular Division, Vanderbilt University, Nashville, TN.
Cristi L GalindoDepartment of Medicine, Cardiovascular Division, Vanderbilt University, Nashville, TN.
Yan Ru SuDepartment of Medicine, Cardiovascular Division, Vanderbilt University, Nashville, TN.
Tarek AbsiDepartment of Cardiothoracic Surgery, Vanderbilt University, Nashville, TN.
Leon M BellanDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN; Department of Mechanical Engineering, Vanderbilt University, Nashville, TN.
Douglas B SawyerDepartment of Medicine, Cardiovascular Division, Vanderbilt University, Nashville, TN.
Hak-Joon SungDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN; Department of Medicine, Cardiovascular Division, Vanderbilt University, Nashville, TN.
Vanderbilt University · US

Funding

Optimizing Cardiovascular Stem Cells for Cardiac Repair and RegenerationU01HL100398 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HATZOPOULOS, ANTONIS · 2009 to 2015
$8.0M
Role of Neuregulin/erbB Signaling in the Adult HeartR01HL068144 · NHLBI · VANDERBILT UNIVERSITY · PI SAWYER, DOUGLAS B · 2001 to 2009
$2.5M
The anti-fibrotic effects of neuregulin in the heartK01HL121045 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GALINDO, CRISTI LARA · 2014 to 2018
$747k
Optimizing Bioactive Hydrogels to Control Angiogenesis and Inflammation in FunctiR21HL091465 · NHLBI · RUTGERS, THE STATE UNIV OF N.J. · PI KOHN, JOACHIM B. · 2009 to 2010
$425k
NHLBI NIH HHS K01 HL121045NHLBI NIH HHS R01 HL068144NHLBI NIH HHS R21 HL091465NHLBI NIH HHS U01 HL100398
6 · The paper itself

Abstract

Despite recent advances in biomimetic substrates, there is still only limited understanding of how the extracellular matrix (ECM) functions in the maintenance of cardiomyocyte (CM) phenotype. In this study, we designed electrospun substrates inspired by morphologic features of non-failing and failing human heart ECM, and examined how these substrates regulate phenotypes of adult and neonatal rat ventricular CMs (ARVM and NRVM, respectively). We found that poly(ε-caprolactone) fiber substrates designed to mimic the organized ECM of a non-failing human heart maintained healthy CM phenotype (evidenced by cell morphology, organized actin/myomesin bands and expression of β-MYH7 and SCN5A.1 and SCN5A.2) compared to both failing heart ECM-mimetic substrates and tissue culture plates. Moreover, culture of ARVMs and NRVMs on aligned substrates showed differences in m- and z-line alignment; with ARVMs aligning parallel to the ECM fibers and the NRVMs aligning perpendicular to the fibers. The results provide new insight into cardiac tissue engineering by illustrating the importance models that mimic the cardiac ECM microenvironment

Identifiers

PMID28042345
PMCPMC5193097
OpenAlexW1423628101

What OpenQuestion holds

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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.