Jahn L, Sadoshima J, Greene A, Parker C, Morgan K G, Izumo S
Molecular Medicine, Division, Beth Israel Hospital, Boston, MA 02215, USA.
J Cell Sci. 1996 Feb;109 ( Pt 2):397-407. doi: 10.1242/jcs.109.2.397.
To create muscle cell lines that conditionally differentiate in vitro we introduced a temperature-sensitive SV40 T antigen by retroviral infection into rat aortic smooth muscle cells (SMCs) and neonatal heart-derived cells. After G418 selection cell lines isolated were characterized at permissive (33 degrees C) and non-permissive (39 degrees C) temperatures. [3H]Thymidine uptake showed tht progression through the cell cycle is greatly reduced at 39 degrees C. Cytoskeletal proteins, such as actins and vimentin did not change significantly after temperature shift, while the number of desmin-positive SMCs significantly increased when cells were switched to 39 degrees C. Heart-derived muscle cells showed sarcomeric myosin heavy chain reactivity only when grown at 39 degrees C. After thrombin stimulation intracellular calcium in both cell types increased severalfold in 39 degrees C-cells but not in 33 degrees C-cells. Whole cell patch-clamp recordings of SMCs and heart-derived cells revealed a strong increase in nicardipine-sensitive Ca2+ current when cells were switched to 39 degrees C. Nicardipine-insensitive Ca2+ current also increased in both cell types at the non-permissive temperature. Na+ current in SMCs was large at 33 degrees C and small or not detectable at 39 degrees C and absent in heart-derived cells. Using a cDNA probe specific for the alpha 1 subunit of the dihydropyridine-sensitive Ca2+ channel we demonstrate a temperature-sensitive expression of the dihydropyridine receptor mRNA in smooth muscle-derived cells but not in heart-derived H10 cells. Our results suggest that upon downregulation of SV40 T antigen these cells become quiescent and exhibit a more differentiated phenotype. These cell lines may provide a useful tool to investigate ion channel- and receptor signal transduction, as well as cell cycle control in smooth and possibly cardiac muscle cell differentiation.
为了创建能在体外进行条件分化的肌肉细胞系,我们通过逆转录病毒感染将温度敏感型SV40 T抗原导入大鼠主动脉平滑肌细胞(SMC)和新生心脏来源的细胞中。经过G418筛选后,对分离得到的细胞系在允许温度(33℃)和非允许温度(39℃)下进行特性鉴定。[3H]胸苷摄取显示,在39℃时细胞周期进程大大减缓。细胞骨架蛋白,如肌动蛋白和波形蛋白,在温度转换后没有显著变化,而当细胞转换到39℃时,结蛋白阳性的SMC数量显著增加。心脏来源的肌肉细胞仅在39℃生长时显示肌节肌球蛋白重链反应性。凝血酶刺激后,两种细胞类型在39℃的细胞中细胞内钙增加了几倍,而在33℃的细胞中则没有增加。对SMC和心脏来源细胞进行全细胞膜片钳记录显示,当细胞转换到39℃时,尼卡地平敏感的Ca2+电流大幅增加。在非允许温度下,两种细胞类型中尼卡地平不敏感的Ca2+电流也增加。SMC中的Na+电流在33℃时较大,在39℃时较小或检测不到,而在心脏来源的细胞中不存在。使用对二氢吡啶敏感的Ca2+通道α1亚基特异的cDNA探针,我们证明二氢吡啶受体mRNA在平滑肌来源的细胞中存在温度敏感型表达,但在心脏来源的H10细胞中不存在。我们的结果表明,在SV40 T抗原下调后,这些细胞进入静止状态并表现出更分化的表型。这些细胞系可能为研究离子通道和受体信号转导以及平滑肌和可能的心肌细胞分化中的细胞周期控制提供有用的工具。