Klewer S E, Krob S L, Kolker S J, Kitten G T
Department of Pediatrics, University of Arizona College of Medicine, Tucson, USA.
Dev Dyn. 1998 Mar;211(3):248-55. doi: 10.1002/(SICI)1097-0177(199803)211:3<248::AID-AJA6>3.0.CO;2-H.
During development, the embryonic atrioventricular (AV) endocardial cushions undergo a morphogenic process to form mature valve leaflets and the membranous septa in the heart. Several extracellular matrix (ECM) proteins are expressed in the developing AV endocardial cushions, but it remains to be established if any specific ECM proteins are necessary for normal cushion morphogenesis. Abnormal development of the cardiac AV valves is a frequent cause of congenital heart defects, particularly in infants with trisomy 21 (Down syndrome). The genes encoding the alpha1 and alpha2 chains of type VI collagen are located on human chromosome 21 within the region thought to be critical for congenital heart defects in trisomy 21 infants. This suggests that the type VI collagen alpha1(VI) and alpha2(VI) chains may be important in normal AV valve morphogenesis. As a first step in understanding the role of type VI collagen in valve development, the authors examined the normal spatial and temporal expression patterns of mRNA and protein for type VI collagen in the embryonic mouse heart. Ribonuclease protection assay analysis demonstrates cardiac expression of the type VI collagen for alpha1(VI), alpha2(VI), and alpha3(VI) transcripts beginning at embryonic days 11-11.5 of mouse development. In situ hybridization studies demonstrate a coordinated pattern of cardiac expression within the AV valves for each type VI collagen chain from embryonic day 11.5 through the neonatal period. Immunohistochemical studies confirm a concentrated type VI collagen localization pattern in the endocardial cushions from the earliest stages of valve development through the neonatal period. These data indicate that type VI collagen is expressed in the developing AV canal in a pattern consistent with cushion tissue mesenchymal cell migration and proliferation, and suggest that type VI collagen plays a role in the morphogenesis of the developing cardiac AV endocardial cushions into the valve leaflets and membranous septa of the heart.
在发育过程中,胚胎房室(AV)心内膜垫经历一个形态发生过程,以形成心脏中的成熟瓣膜小叶和膜性间隔。几种细胞外基质(ECM)蛋白在发育中的房室心内膜垫中表达,但对于正常垫形态发生是否需要任何特定的ECM蛋白仍有待确定。心脏房室瓣的异常发育是先天性心脏缺陷的常见原因,尤其是在21三体综合征(唐氏综合征)婴儿中。编码VI型胶原α1和α2链的基因位于人类21号染色体上被认为对21三体综合征婴儿先天性心脏缺陷至关重要的区域。这表明VI型胶原α1(VI)和α2(VI)链可能在正常房室瓣形态发生中起重要作用。作为了解VI型胶原在瓣膜发育中作用的第一步,作者研究了胚胎小鼠心脏中VI型胶原mRNA和蛋白的正常时空表达模式。核糖核酸酶保护分析表明,从小鼠发育的胚胎第11 - 11.5天开始,心脏中就有VI型胶原α1(VI)、α2(VI)和α3(VI)转录本的表达。原位杂交研究表明,从胚胎第11.5天到新生儿期,每种VI型胶原链在房室瓣内的心脏表达呈现协调模式。免疫组织化学研究证实,从瓣膜发育的最早阶段到新生儿期,VI型胶原在内膜垫中呈集中定位模式。这些数据表明,VI型胶原在发育中的房室管中以与垫组织间充质细胞迁移和增殖一致的模式表达,并表明VI型胶原在发育中的心脏房室心内膜垫向心脏瓣膜小叶和膜性间隔的形态发生中起作用。