Cardiac fiber orientation and the left-right asymmetry determining mechanism

被引:15
作者
Delhaas, T
Decaluwe, W
Rubbens, M
Kerckhoffs, R
Arts, T
机构
[1] Univ Hosp, Dept Pediat, NL-6202 AZ Maastricht, Netherlands
[2] Univ Limburg, Dept Physiol, NL-6200 MD Maastricht, Netherlands
[3] Univ Limburg, Dept Biophys, NL-6200 MD Maastricht, Netherlands
[4] Tech Univ Eindhoven, Dept Biomed Technol, NL-5512 AZ Eindhoven, Netherlands
来源
CARDIAC ENGINEERING: FROM GENES AND CELLS TO STRUCTURE AND FUNCTION | 2004年 / 1015卷
关键词
left-right asymmetry; cardiac looping; cardiac development; heart defects; congenital; myocardium; myofiber; situs solitus; situs inversustotalis;
D O I
10.1196/annals.1302.016
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
The invariant nature of body situs within and across vertebrate species implies that a highly conserved pathway controls the specification of the left-right (L/R) axis. Situs-specific morphogenesis begins at the end of this pathway and leads to normal organ arrangement, also known as situs solitus. Occasionally, individuals have a complete, mirror image reversal of this asymmetry, called situs inversus totalis (SIT). In these individuals, gross anatomy is mirror imaged. However, the helical myofiber pattern within the left ventricle (LV) wall is only partially mirror imaged: apical and superficial basal fiber orientation are as in normal persons, whereas the deeper basal layers have an inverted fiber orientation. Because of this bivalent fiber orientation pattern, LV deformation in humans with SIT is mirror imaged only near the base, but near the apex it is as in normal subjects. Apparently, the embryonic L/R controlling genetic pathway does determine situs-specific gross anatomy morphogenesis, but it is not the only factor regulating fiber architecture within the LV wall.
引用
收藏
页码:190 / 201
页数:12
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