Evidence map›Paper›PMID 28116799›Full record

ReviewThe Journal of physiology2017

In vitro models of the cardiac microenvironment to study myocyte and non-myocyte crosstalk: bioinspired approaches beyond the polystyrene dish.

Celinda M Kofron, Ulrike Mende

Open access · greenAbstract readReview
In one paragraph

Review in The Journal of physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
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  6. Review
  7. Review
  8. Review
  9. Review
  10. Lab-on-Chip Microsystems forFrontiers in bioengineering and biotechnology · 2022
    Review
  11. Metabolic remodeling in takotsubo syndrome.Frontiers in cardiovascular medicine · 2022
    Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Regulators of cardiac fibroblast cell state.Matrix biology : journal of the International Society for Matrix Biology · 2020
    Review
  18. Review
  19. Review
  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

2 authors at 1 institution in 1 country.

Celinda M KofronCardiovascular Research Center, Cardiovascular Institute, Rhode Island Hospital and Alpert Medical School of Brown University, Providence, RI, USA.
Ulrike MendeCardiovascular Research Center, Cardiovascular Institute, Rhode Island Hospital and Alpert Medical School of Brown University, Providence, RI, USA.ORCID 0000-0002-3362-6072
Brown University · US

Funding

Regulation of Gq Signaling in Cardiac Fibroblasts and its Role in Cardiac RemodelR01HL114784 · NHLBI · RHODE ISLAND HOSPITAL · PI MENDE, ULRIKE · 2013 to 2016
$2.0M
Role of Fibroblasts in Cardiac Remodeling and Regulation of CardiomyocytesF32HL126311 · NHLBI · RHODE ISLAND HOSPITAL · PI KOFRON, CELINDA MICHELLE · 2015 to 2016
$90k
NHLBI NIH HHS F32 HL126311NHLBI NIH HHS R01 HL114784
6 · The paper itself

Abstract

The heart is a complex pluricellular organ composed of cardiomyocytes and non-myocytes including fibroblasts, endothelial cells and immune cells. Myocytes are responsible for electrical conduction and contractile force generation, while the other cell types are responsible for matrix deposition, vascularization, and injury response. Myocytes and non-myocytes are known to communicate and exert mutual regulatory effects. In concert, they determine the structural, electrical and mechanical characteristics in the healthy and remodelled myocardium. Dynamic crosstalk between myocytes and non-myocytes plays a crucial role in stress/injury-induced hypertrophy and fibrosis development that can ultimately lead to heart failure and arrhythmias. Investigations of heterocellular communication in the myocardium are hampered by the intricate interspersion of the different cell types and the complexity of the tissue architecture. In vitro models have facilitated investigations of cardiac cells in a direct and controllable manner and have provided important functional and mechanistic insights. However, these cultures often lack regulatory input from the other cell types as well as additional topographical, electrical, mechanical and biochemical cues from the cardiac microenvironment that all contribute to modulating cell differentiation, maturation, alignment, function and survival. Advancements in the development of more complex pluricellular physiological platforms that incorporate diverse cues from the myocardial microenvironment are expected to lead to more physiologically relevant cardiac tissue-like in vitro models for mechanistic biological research, disease modelling, therapeutic target identification, drug testing and regeneration.

Indexed as

AnimalsArrhythmias, CardiacCell CommunicationFibroblastsFibrosisHumansHypertrophyMyocardial ContractionMyocardiumMyocytes, CardiacPolystyrenesPolystyrenes2D culture3D culturecardiac fibroblastscardiac myocytescrosstalkendothelial cellsmyocardiumtissue engineering

Identifiers

PMID28116799
PMCPMC5471366
OpenAlexW2581012516

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.