New frontiers in molecular pediatric cardiology

被引:6
作者
Dees, E [1 ]
Baldwin, HS [1 ]
机构
[1] Vanderbilt Univ, Med Ctr N D2200, Div Pediat Cardiol, Nashville, TN 37232 USA
关键词
D O I
10.1097/00008480-200210000-00011
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Numerous advances in understanding the molecular basis of congenital heart disease have been published in the past year. Highlights are reviewed, focusing on two major topics: genetic syndromes and cardiac organogenesis. Genetic syndromes are discussed in the context of complementary data from targeted mutations in animals and genetic mapping studies in humans. These include the DiGeorge, Holt-Oram, Alagille, familial primary pulmonary hypertension, and Noonan syndromes. Novel concepts in cardiac organogenesis are discussed, including the existence and contribution of an anterior heart field to the developing cardiac outflow tract, novel cell-cell signaling involving migrating neural crest, the origins of the conduction system and initial embryonic heartbeat, and the possibility of a population of cardiac stem cells in the adult heart. The studies reviewed have potential clinical relevance in the near future and will be of interest to the clinician interested in congenital heart disease. (C) 2002 Lippincott Williams Wilkins, Inc.
引用
收藏
页码:627 / 633
页数:7
相关论文
共 38 条
[1]   Myocyte renewal and ventricular remodelling [J].
Anversa, P ;
Nadal-Ginard, B .
NATURE, 2002, 415 (6868) :240-243
[2]   Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome [J].
Basson, CT ;
Bachinsky, DR ;
Lin, RC ;
Levi, T ;
Elkins, JA ;
Soults, J ;
Grayzel, D ;
Kroumpouzou, E ;
Traill, TA ;
LeblancStraceski, J ;
Renault, B ;
Kucherlapati, R ;
Seidman, JG ;
Seidman, CE .
NATURE GENETICS, 1997, 15 (01) :30-35
[3]   Evidence that human cardiac myocytes divide after myocardial infarction (Publication with Expression of Concern. See vol. 379, pg. 1870, 2018) [J].
Beltrami, AP ;
Urbanek, K ;
Kajstura, J ;
Yan, SM ;
Finato, N ;
Bussani, R ;
Nadal-Ginard, B ;
Silvestri, F ;
Leri, A ;
Beltrami, CA ;
Anversa, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (23) :1750-1757
[4]   BMP type II receptor is required for gastrulation and early development of mouse embryos [J].
Beppu, H ;
Kawabata, M ;
Hamamoto, T ;
Chytil, A ;
Minowa, O ;
Noda, T ;
Miyazono, K .
DEVELOPMENTAL BIOLOGY, 2000, 221 (01) :249-258
[5]  
Brown CB, 2001, DEVELOPMENT, V128, P3071
[6]   A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease [J].
Bruneau, BG ;
Nemer, G ;
Schmitt, JP ;
Charron, F ;
Robitaille, L ;
Caron, S ;
Conner, DA ;
Gessler, M ;
Nemer, M ;
Seidman, CE ;
Seidman, JG .
CELL, 2001, 106 (06) :709-721
[7]   Mice mutant for Egfr and Shp2 have defective cardiac semilunar valvulogenesis [J].
Chen, BB ;
Bronson, RT ;
Klaman, LD ;
Hampton, TG ;
Wang, JF ;
Green, PJ ;
Magnuson, T ;
Douglas, PS ;
Morgan, JP ;
Neel, BG .
NATURE GENETICS, 2000, 24 (03) :296-299
[8]  
Feiner L, 2001, DEVELOPMENT, V128, P3061
[9]   DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1 [J].
Jerome, LA ;
Papaioannou, VE .
NATURE GENETICS, 2001, 27 (03) :286-291
[10]   Myocyte proliferation in end-stage cardiac failure in humans [J].
Kajstura, J ;
Leri, A ;
Finato, N ;
Di Loreto, C ;
Beltrami, CA ;
Anversa, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (15) :8801-8805