2015年第42卷第4期目录
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封面故事:心血管系统结构及功能的异常严重威胁人类的健康.现大量研究表明T-box基因家族在脊椎动物心脏结构及功能的发生发育过程中意义重大.其中,转录因子Tbx18作为T-box家族成员之一,其有可能参与心脏损伤后心肌及血管的修复及再生,故明确其在心脏结构及功能发育中的具体作用显得至关重要.既往研究已表明Tbx18对心脏窦房结的形成及分化起决定性作用,但其对心脏血管及心肌结构的形成是否起决定性作用仍不明确.本实验研究中,我们采用建立的Tbx18-Cre/ Rosa26R-EYFP和Tbx18-Cre/ Rosa26R-LacZ两种谱系示踪小鼠模型,特异性示踪Tbx18在心血管系统结构形成中的命运,并比较了Tbx18:Cre/Cre基因敲除小鼠与野生型小鼠心脏室壁结构及冠状血管结构发育情况.最终得出Tbx18参与小鼠心脏血管平滑肌及室间隔结构的形成,但其在小鼠心脏腔室结构及冠状血管结构形成过程中不是必需的这一结论,为进一步探索Tbx18在心血管结构形成中的作用提供了实验依据.
(汪 浩,佘 强,高凌志,查承沁,杜建霖,景小东. Tbx18对小鼠心脏冠状血管及室壁结构发育的影响,本期第348~355页)
Cover Story:Using Tbx18 lineage tracer mouse model and Tbx18 conditional knockout mouse model to explore the functions of Tbx18 in the development of the structures of coronary vascular and ventricular wall. Two types of lineage tracer mouse models are established: Tbx18-Cre/Rosa26R-EYFP and Tbx18-Cre/Rosa26R-LacZ, and Tbx18:Cre/Cre gene knockout mouse model are used in the experiment. We trace the fate of Tbx18 in the formation of the vascular and myocardial structure in the cardiovascular system by immunofluorescence and X-gal staining techniques. And we compare the structure of coronary vascular and ventricular wall in Tbx18:Cre/Cre gene knockout mouse with wild-type mouse by whole-mount PECAM immunohistochemistry, HE staining, immunohistochemistry and immunofluorescence techniques. The trace of Tbx18 shows that Tbx18 contributes to the structure of the mouse coronary vessels and interventricular septum, and Tbx18 expression co-locolize with smooth muscle cells. The comparison between Tbx18:Cre/Cre gene knockout mouse and wild-type mouse shows that the knockout mouse can form normal coronary vascular system, and there is no difference between the thickness of the ventricular wall and the interventricular septum. The gene Tbx18 contributes to the heart vascular smooth muscle and interventricular septum, but it is not necessary in the formation of coronary vascular structure and the heart chamber structure.
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综述与专论
研究报告
技术与方法
前沿透视
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