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Morphological Observation of the Cashmere goat Fetal Fibroblasts after mTOR Kinase Inhibition with Combination of Fluorescent Dyes and Confocal Cell Imaging

机译:用荧光染料和共焦细胞成像组合MTOR激酶抑制作用羊绒山羊胎儿成纤维细胞的形态学观察

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The mammalian target of rapamycin (mTOR) is a kind of Ser/Thr kinase in mammalian cells. It can recruit and integrate input signals from nutrients, growth factors, energy and environmental stress to regulate cell growth and proliferation via different cellular processes. This study uses the fetal fibroblasts of Inner Mongolia Cashmere goat (Capra hircas) to prove that the mTOR plays a critical role in formation of the cell cytoskeleton structure. The mTOR kinase activity was inhibited in Inner Mongolia Cashmere goat fetal fibroblasts (GFb) after treatment with CCI-779 (temsirolimus), an mTOR specific inhibitor for 48 h. The results showed that GFb cells were sensitive to CCI-779. GFb cells morphology and its cytoskeleton structure changed under confocal laser scanning microscopy stained with the Fluorescent phalloidin (50μg/ml, Phalloidin- FITC5282) which combines with F-actin. In summary, mTOR signaling pathway was proved to be functional in GFb cells and acts as a key regulator to form cell structure. The Morphological results indicated that perhaps the synthesis of microfilament or organization of cytoskeleton was disrupted in GFb cells when mTOR was inhibited.
机译:哺乳动物的雷帕霉素(mTOR)的靶标是哺乳动物细胞中的一种SER / THR激酶。它可以招募和整合来自营养,生长因子,能量和环境应力的输入信号,通过不同的细胞过程调节细胞生长和增殖。本研究使用内蒙古羊绒山羊(Capra Hircas)的胎儿成纤维细胞来证明MTOR在形成细胞细胞骨架结构中发挥着关键作用。用CCI-779(Temsirolimus),MTOR特异性抑制剂48小时,在内蒙古羊绒爬虫胎儿成纤维细胞(GFB)中抑制了MTOR激酶活性。结果表明,GFB细胞对CCI-779敏感。 GFB细胞形态及其细胞骨架结构在与荧光阴蛋白(50μg/ mL,Phalloidin-FitC5282)染色的共聚焦激光扫描显微镜下改变,其与F-Actin结合。总之,证明了MTOR信号传导途径在GFB细胞中具有功能性,并作为关键调节器以形成细胞结构。形态学结果表明,当MTOR被抑制时,可能在GFB细胞中破坏细胞骨骼或细胞骨架组织的合成。

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