Evidence map›Paper›PMID 22906538›Full record

ArticleJournal of molecular and cellular cardiology2012

Collagen XIV is important for growth and structural integrity of the myocardium.

Ge Tao, Agata K Levay, Jacqueline D Peacock, Danielle J Huk, Sarah N Both, Nicole H Purcell, Jose R Pinto, Maarten L Galantowicz, Manuel Koch, Pamela A Lucchesi and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular and cellular cardiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
1.5field-weighted citation impact, top 21% 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

47 citing papers in PubMed, 85 citations in OpenAlex.

  1. Observational
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  9. Procollagen IIA mediates positive feedback control of the mouse cardiogenic transcriptional network.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  14. IdentifyingBiomolecules · 2024
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  19. Cardiomyocyte-fibroblast crosstalk in the postnatal heart.Frontiers in cell and developmental biology · 2023
    Review
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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

12 authors at 7 institutions in 2 countries.

Ge TaoMolecular, Cell and Developmental Biology Graduate Program, Leonard M. Miller School of Medicine, Miami, FL 33101, USA.
Agata K Levay
Jacqueline D Peacock
Danielle J Huk
Sarah N Both
Nicole H Purcell
Jose R Pinto
Maarten L Galantowicz
Manuel Koch
Pamela A Lucchesi
David E Birk
Joy Lincoln
University of Miami · USNationwide Children's Hospital · USFlorida State University · USThe Ohio State University · USUniversity of California, San Diego · USUniversity of Cologne · DEUniversity of South Florida · US

Funding

Molecular regulation of heart valve development and function.R01HL091878 · NHLBI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LINCOLN, JOY · 2008 to 2012
$2.2M
NHLBI NIH HHS HL091878NHLBI NIH HHS R01 HL091878
6 · The paper itself

Abstract

Collagen XIV is a fibril-associated collagen with an interrupted triple helix (FACIT). Previous studies have shown that this collagen type regulates early stages of fibrillogenesis in connective tissues of high mechanical demand. Mice null for Collagen XIV are viable, however formation of the interstitial collagen network is defective in tendons and skin leading to reduced biomechanical function. The assembly of a tightly regulated collagen network is also required in the heart, not only for structural support but also for controlling cellular processes. Collagen XIV is highly expressed in the embryonic heart, notably within the cardiac interstitium of the developing myocardium, however its role has not been elucidated. To test this, we examined cardiac phenotypes in embryonic and adult mice devoid of Collagen XIV. From as early as E11.5, Col14a1(-/-) mice exhibit significant perturbations in mRNA levels of many other collagen types and remodeling enzymes (MMPs, TIMPs) within the ventricular myocardium. By post natal stages, collagen fibril organization is in disarray and the adult heart displays defects in ventricular morphogenesis. In addition to the extracellular matrix, Col14a1(-/-) mice exhibit increased cardiomyocyte proliferation at post natal, but not E11.5 stages, leading to increased cell number, yet cell size is decreased by 3 months of age. In contrast to myocytes, the number of cardiac fibroblasts is reduced after birth associated with increased apoptosis. As a result of these molecular and cellular changes during embryonic development and post natal maturation, cardiac function is diminished in Col14a1(-/-) mice from 3 months of age; associated with dilation in the absence of hypertrophy, and reduced ejection fraction. Further, Col14a1 deficiency leads to a greater increase in left ventricular wall thickening in response to pathological pressure overload compared to wild type animals. Collectively, these studies identify a new role for type XIV collagen in the formation of the cardiac interstitium during embryonic development, and highlight the importance of the collagen network for myocardial cell survival, and function of the working myocardium after birth.

Indexed as

AnimalsCell ProliferationCollagenGlycoproteinsHeartHeart VentriclesHypertrophy, Left VentricularIn Vitro TechniquesMaleMiceMice, TransgenicMyocardial ContractionMyocardiumMyocytes, CardiacStroke VolumeTranscription, GeneticCol14a1 protein, mouseCollagenGlycoproteins

Identifiers

PMID22906538
PMCPMC3472103
OpenAlexW2019119739

What OpenQuestion holds

Textmetadata
LicenceTDM
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.