Cell lineages and tissue boundaries in cardiac arterial and venous poles - Developmental patterns, animal models, and implications for congenital vascular diseases

被引:9
作者
Ausoni, S
Sartore, S
机构
[1] Univ Padua, Dept Biomed Sci, I-35121 Padua, Italy
[2] CNR, Ctr Muscle Biol, Padua, Italy
关键词
congenital cardiovascular diseases; tissue boundaries; outflow tract; inflow tract; animal models;
D O I
10.1161/01.ATV.21.3.312
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multiple cell populations with different embryological histories are involved in the morphogenesis of the cardiac arterial and venous poles as well as in the correct alignment and connection of the developing vessels with the cardiac chambers. Formation of the aorta and the pulmonary trunk is a complicated process orchestrated via a specific sequence of highly integrated spatiotemporal events of cell proliferation, migration, differentiation, and apoptosis. The peculiar susceptibility of this intricate cell network to be altered explains the frequency of congenital cardiovascular diseases of the arterial and venous poles. We review this topic from the "vascular point of view," putting major emphasis on (1) the existence of different cell lineages from which smooth muscle cells of the aorticopulmonary trunk can be derived, (2) the establishment of cell/tissue boundaries in the cardiovascular connecting regions, and (3) the animal models that can mimic human congenital defects of the arterial and venous poles of the heart.
引用
收藏
页码:312 / 320
页数:9
相关论文
共 102 条
[61]  
MORRISONGRAHAM K, 1992, DEVELOPMENT, V115, P133
[62]   HRT1, HRT2, and HRT3:: A new subclass of bHLH transcription factors marking specific cardiac, somitic, and pharyngeal arch segments [J].
Nakagawa, O ;
Nakagawa, M ;
Richardson, JA ;
Olson, EN ;
Srivastava, D .
DEVELOPMENTAL BIOLOGY, 1999, 216 (01) :72-84
[63]   PATHOGENESIS OF PERSISTENT TRUNCUS ARTERIOSUS AND DEXTROPOSED AORTA IN THE CHICK-EMBRYO AFTER NEURAL CREST ABLATION [J].
NISHIBATAKE, M ;
KIRBY, ML ;
VANMIEROP, LHS .
CIRCULATION, 1987, 75 (01) :255-264
[64]   CELL ORIGINS AND TISSUE BOUNDARIES DURING OUTFLOW TRACT DEVELOPMENT [J].
NODEN, DM ;
POELMANN, RE ;
GROOT, ACG .
TRENDS IN CARDIOVASCULAR MEDICINE, 1995, 5 (02) :69-75
[65]   Individual haploinsufficient loci and the complex phenotype of DiGeorge syndrome [J].
Novelli, G ;
Amati, F ;
Dallapiccola, B .
MOLECULAR MEDICINE TODAY, 2000, 6 (01) :10-11
[66]   The signaling pathway mediated by the type IIB activin receptor controls axial patterning and lateral asymmetry in the mouse [J].
Oh, SP ;
Li, E .
GENES & DEVELOPMENT, 1997, 11 (14) :1812-1826
[67]   Smooth muscle cells and fibroblasts of the coronary arteries derive from epithelial-mesenchymal transformation of the epicardium [J].
Peeters, MPFMV ;
Gittenberger-de Groot, AC ;
Mentink, MMT ;
Poelmann, RE .
ANATOMY AND EMBRYOLOGY, 1999, 199 (04) :367-378
[68]   The orphan nuclear receptor COUP-TFII is required for angiogenesis and heart development [J].
Pereira, FA ;
Qiu, YH ;
Zhou, G ;
Tsai, MJ ;
Tsai, SY .
GENES & DEVELOPMENT, 1999, 13 (08) :1037-1049
[69]   Immunohistochemical evidence for a mesothelial contribution to the ventral wall of the avian aorta [J].
Pérez-Pomares, JM ;
Macías-López, D ;
García-Garrido, L ;
Muñoz-Chápuli, R .
HISTOCHEMICAL JOURNAL, 1999, 31 (12) :771-779
[70]  
PEXIEDER T, 1995, DEVELOPMENTAL MECHANISMS OF HEART DISEASE, P227