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Open AccessJournal ArticleDOI

Heart Valve Development: Regulatory networks in development and disease

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TLDR
The cellular and molecular mechanisms underlying the early development of valve progenitors and establishment of normal valve structure and function are reviewed.
Abstract
In recent years, significant advances have been made in the definition of regulatory pathways that control normal and abnormal cardiac valve development. Here, we review the cellular and molecular mechanisms underlying the early development of valve progenitors and establishment of normal valve structure and function. Regulatory hierarchies consisting of a variety of signaling pathways, transcription factors, and downstream structural genes are conserved during vertebrate valvulogenesis. Complex intersecting regulatory pathways are required for endocardial cushion formation, valve progenitor cell proliferation, valve cell lineage development, and establishment of extracellular matrix compartments in the stratified valve leaflets. There is increasing evidence that the regulatory mechanisms governing normal valve development also contribute to human valve pathology. In addition, congenital valve malformations are predominant among diseased valves replaced late in life. The understanding of valve developmental mechanisms has important implications in the diagnosis and management of congenital and adult valve disease.

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Journal ArticleDOI

Zebrafish as a model to study cardiac development and human cardiac disease

TL;DR: In this review, recent discoveries in the field of cardiac development are discussed and specific cases in which the zebrafish has been used to model human congenital and acquired cardiac diseases are discussed.
Journal ArticleDOI

Heart Valve Structure and Function in Development and Disease

TL;DR: The mature heart valves are made up of highly organized extracellular matrix (ECM) and valve interstitial cells (VICs) surrounded by an endothelial cell layer that confer distinct biomechanical properties to the leaflets and supporting structures.
Journal ArticleDOI

Endocardial and Epicardial Epithelial to Mesenchymal Transitions in Heart Development and Disease

TL;DR: The role and molecular regulation of endocardial and epicardial EMT in fetal heart development is reviewed, and key literature implicating reactivation of end Cardiomyocyte and EpicardialEMT in adult heart disease is summarized.
Book ChapterDOI

Transcription Factor Pathways and Congenital Heart Disease

TL;DR: By understanding the interaction partners, transcriptional targets, and upstream activators of these core cardiac transcription factors, additional information about normal heart formation and further insight into genes and pathways affected in congenital heart disease should result.
Journal ArticleDOI

Cellular Mechanisms of Aortic Valve Calcification

TL;DR: Calcification of the aortic valve is now understood to be an active process that involves the coordinated actions of resident valve endothelial and interstitial cells, circulating inflammatory and immune cells, and bone marrow-derived cells that form matrix vesicles that serve as a nidus for microcalcifications.
References
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Journal ArticleDOI

The incidence of congenital heart disease

TL;DR: The causes of variation are determined, there is no evidence for differences in incidence in different countries or times, and the incidences of individual major forms of CHD were determined from 44 studies.
Journal ArticleDOI

Mutations in NOTCH1 cause aortic valve disease

TL;DR: It is shown that mutations in the signalling and transcriptional regulator NOTCH1 cause a spectrum of developmental aortic valve anomalies and severe valve calcification in non-syndromic autosomal-dominant human pedigrees.
Journal ArticleDOI

Defects in mesoderm, neural tube and vascular development in mouse embryos lacking fibronectin

TL;DR: Mice generated in which the fibronectin gene is inactivated display shortened anterior-posterior axes, deformed neural tubes and severe defects in mesodermally derived tissues, proving that fibronECTin is required for embryogenesis.
Journal ArticleDOI

Fate of the mammalian cardiac neural crest.

TL;DR: A two-component genetic system based on Cre/lox recombination is employed to label indelibly the entire mouse neural crest population at the time of its formation, and to detect it at any time thereafter.
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