Chen Jin-Wen, Zhou Bin, Yu Qian-Chun, Shin Sangyoon J, Jiao Kai, Schneider Michael D, Baldwin H Scott, Bergelson Jeffrey M
Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, USA.
Circ Res. 2006 Apr 14;98(7):923-30. doi: 10.1161/01.RES.0000218041.41932.e3. Epub 2006 Mar 16.
The coxsackievirus and adenovirus receptor (CAR), which mediates infection by the viruses most commonly associated with myocarditis, is a transmembrane component of specialized intercellular junctions, including the myocardial intercalated disc; it is known to mediate cell-cell recognition, but its natural function is poorly understood. We used conditional gene targeting to investigate the possible functions of CAR during embryonic development, generating mice with both germline and tissue-specific defects in CAR expression. Homozygous germline deletion of CAR exon 2 or cardiomyocyte-specific gene deletion at embryonic day 10 (E10) mediated by Cre recombinase expressed under the control of the cardiac troponin T promoter resulted in death by E12.5; embryos showed marked cardiac abnormalities by E10.5, with hyperplasia of the left ventricular myocardium, distention of the cardinal veins, and abnormalities of sinuatrial valves. Within the hyperplastic left ventricle, increased numbers of proliferating cells were evident; persistent expression of N-myc in the hyperplastic myocardium and attenuated expression of the trabecular markers atrial natriuretic factor and bone morphogenic protein 10 indicated that proliferating cardiomyocytes had failed to differentiate and form normal trabeculae. In electron micrographs, individual CAR-deficient cardiomyocytes within the left ventricle appeared normal, but intercellular junctions were ill-formed or absent, consistent with the known function of CAR as a junctional molecule; myofibrils were also poorly organized. When cardiomyocyte-specific deletion occurred somewhat later (by E11, mediated by Cre under control of the alpha-myosin heavy chain promoter), animals survived to adulthood and did not have evident cardiac abnormalities. These results indicate that during a specific temporal window, CAR expression on cardiomyocytes is essential for normal cardiac development. In addition, the results suggest that CAR-mediated intercellular contacts may regulate proliferation and differentiation of cardiomyocytes within the embryonic left ventricular wall.
柯萨奇病毒和腺病毒受体(CAR)介导了最常与心肌炎相关的病毒的感染,它是包括心肌闰盘在内的特殊细胞间连接的跨膜成分;已知其介导细胞间识别,但其天然功能仍知之甚少。我们利用条件性基因靶向技术研究胚胎发育过程中CAR的可能功能,构建了CAR表达存在种系和组织特异性缺陷的小鼠。通过在心肌肌钙蛋白T启动子控制下表达的Cre重组酶介导,在胚胎第10天(E10)对CAR外显子2进行纯合种系缺失或心肌细胞特异性基因缺失,导致小鼠在E12.5时死亡;胚胎在E10.5时出现明显的心脏异常,包括左心室心肌增生、主静脉扩张和窦房瓣异常。在增生的左心室内,增殖细胞数量明显增加;增生心肌中N-myc持续表达,小梁标志物心房钠尿肽和骨形态发生蛋白10表达减弱,表明增殖的心肌细胞未能分化并形成正常小梁。在电子显微镜下,左心室内单个CAR缺陷的心肌细胞看起来正常,但细胞间连接形成不良或缺失,这与CAR作为连接分子的已知功能一致;肌原纤维也排列紊乱。当心肌细胞特异性缺失发生在稍晚的时候(在α-肌球蛋白重链启动子控制下由Cre介导,在E11时),动物存活至成年且没有明显的心脏异常。这些结果表明,在特定的时间窗口内,心肌细胞上的CAR表达对于正常心脏发育至关重要。此外,结果表明CAR介导的细胞间接触可能调节胚胎左心室壁中心肌细胞的增殖和分化。