Literature DB >> 10359559

A novel role for cardiac neural crest in heart development.

K Waldo1, M Zdanowicz, J Burch, D H Kumiski, H A Stadt, R E Godt, T L Creazzo, M L Kirby.   

Abstract

Ablation of premigratory cardiac neural crest results in defective development of the cardiac outflow tract. The purpose of the present study was to correlate the earliest functional and morphological changes in heart development after cardiac neural crest ablation. Within 24 hours after neural crest ablation, the external morphology of the hearts showed straight outflow limbs, tighter heart loops, and variable dilations. Incorporation of bromodeoxyuridine in myocytes, an indication of proliferation, was doubled after cardiac neural crest ablation. The myocardial calcium transients, which are a measure of excitation-contraction coupling, were depressed by 50% in both the inflow and outflow portions of the looped heart tube. The myocardial transients could be rescued by replacing the cardiac neural crest. The cardiac jelly produced by the myocardium was distributed in an uneven, rather than uniform, pattern. An extreme variability in external morphology could be attributed to the uneven distribution of cardiac jelly. In the absence of cardiac neural crest, the myocardium was characterized by somewhat disorganized myofibrils that may be a result of abnormally elevated proliferation. In contrast, endocardial development appeared normal, as evidenced by normal expression of fibrillin-2 protein (JB3 antigen) and normal formation of cushion mesenchyme and trabeculae. The signs of abnormal myocardial development coincident with normal endocardium suggest that the presence of cardiac neural crest cells is necessary for normal differentiation and function of the myocardium during early heart development. These results indicate a novel role for neural crest cells in myocardial maturation.

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Year:  1999        PMID: 10359559      PMCID: PMC408374          DOI: 10.1172/JCI6501

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  49 in total

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  27 in total

1.  FGF-8 in the ventral pharynx alters development of myocardial calcium transients after neural crest ablation.

Authors:  M J Farrell; J L Burch; K Wallis; L Rowley; D Kumiski; H Stadt; R E Godt; T L Creazzo; M L Kirby
Journal:  J Clin Invest       Date:  2001-06       Impact factor: 14.808

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Journal:  Birth Defects Res C Embryo Today       Date:  2004-06

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Authors:  Chieh-Yu Lin; Chien-Jung Lin; Chen-Hao Chen; Richard M Chen; Bin Zhou; Ching-Pin Chang
Journal:  J Mol Cell Cardiol       Date:  2012-01-26       Impact factor: 5.000

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Authors:  Michael Olaopa; Hong-ming Zhou; Paige Snider; Jian Wang; Robert J Schwartz; Anne M Moon; Simon J Conway
Journal:  Dev Biol       Date:  2011-05-12       Impact factor: 3.582

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Authors:  Lindsy M Peterson; Shi Gu; Ganga Karunamuni; Michael W Jenkins; Michiko Watanabe; Andrew M Rollins
Journal:  Biomed Opt Express       Date:  2017-02-24       Impact factor: 3.732

Review 6.  Developmental origin and lineage plasticity of endogenous cardiac stem cells.

Authors:  Maria Paola Santini; Elvira Forte; Richard P Harvey; Jason C Kovacic
Journal:  Development       Date:  2016-04-15       Impact factor: 6.868

7.  Cardiac neural crest ablation results in early endocardial cushion and hemodynamic flow abnormalities.

Authors:  Pei Ma; Shi Gu; Ganga H Karunamuni; Michael W Jenkins; Michiko Watanabe; Andrew M Rollins
Journal:  Am J Physiol Heart Circ Physiol       Date:  2016-08-19       Impact factor: 4.733

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Journal:  Exp Clin Cardiol       Date:  2001

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Authors:  Reda H ElMazoudy; Gamal A Bekhet
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10.  BMP receptor IA is required in mammalian neural crest cells for development of the cardiac outflow tract and ventricular myocardium.

Authors:  Rolf W Stottmann; Murim Choi; Yuji Mishina; Erik N Meyers; John Klingensmith
Journal:  Development       Date:  2004-04-08       Impact factor: 6.868

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