Matsuda Takahisa, Takahashi Kyoko, Nariai Tetsurou, Ito Takashi, Takatani Tomoka, Fujio Yasushi, Azuma Junichi
Department of Clinical Evaluation of Medicines and Therapeutics, Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita City, Osaka 565-0871, Japan.
Biochem Biophys Res Commun. 2005 Jan 7;326(1):228-32. doi: 10.1016/j.bbrc.2004.11.019.
Mechanical stretch has been implicated as the growth stimuli in the heart. Physiologically, mechanical stretch is reported to contribute to the orientation of cardiomyocytes, though the molecular mechanism remains to be elucidated. This study was designed to make clear functional significances of N-cadherin in plasticity of cell alignment in response to mechanical stretch. Neonatal rat cardiomyocytes, cultured on silicone dishes, were subjected to artificial uniaxial cyclic stretch. Mechanical stretch was started at certain times (3-75h) after seeding and continued for 24h. Stretch stimulation in 3h after cultivation promoted cell orientation running parallel to tension direction. In contrast, cardiac myocytes fail to align when exposed to stretch 24-75h after cultivation. To address the importance of N-cadherin in the responsiveness to stretch, the expression and distribution of N-cadherin were analyzed. Immediately after seeding, N-cadherin showed dispersed distributions. During cultivation, N-cadherin localized to cell-cell contacts accompanied by the upregulation of its protein. Next, to investigate influence of cell-cell adhesion, cardiomyocytes cultured for 72h were replated by trypsin treatment and exposed to stretch 3h after replating. The cardiomyocytes replated by trypsinization were oriented in parallel to tension direction by mechanical stretch. Finally, adenoviral transfection of dominant-negative N-cadherin recovered the ability to exhibit cell orientation in response to stretch. Our results suggested that N-cadherin was involved in the oriented responses of cardiomyocytes induced by mechanical stretch.
机械牵张被认为是心脏生长的刺激因素。据生理研究报道,机械牵张有助于心肌细胞的定向排列,但其分子机制仍有待阐明。本研究旨在明确N-钙黏蛋白在响应机械牵张时细胞排列可塑性中的功能意义。将新生大鼠心肌细胞培养在硅胶培养皿上,进行人工单轴循环牵张。在接种后的特定时间(3-75小时)开始机械牵张,并持续24小时。培养3小时后进行牵张刺激可促进细胞沿张力方向平行排列。相反,培养24-75小时后暴露于牵张的心肌细胞无法排列。为了探讨N-钙黏蛋白在对牵张反应中的重要性,分析了N-钙黏蛋白的表达和分布。接种后立即,N-钙黏蛋白呈分散分布。在培养过程中,N-钙黏蛋白定位于细胞间接触部位,同时其蛋白表达上调。接下来,为了研究细胞间黏附的影响,对培养72小时的心肌细胞进行胰蛋白酶处理后重新接种,并在重新接种3小时后进行牵张。经胰蛋白酶消化后重新接种的心肌细胞通过机械牵张沿张力方向排列。最后,腺病毒转染显性负性N-钙黏蛋白恢复了心肌细胞对牵张产生定向反应的能力。我们的结果表明,N-钙黏蛋白参与了机械牵张诱导的心肌细胞定向反应。