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Mitochondrial imaging in dorsal root ganglion neurons following the application of inducible adenoviral vector expressing two fluorescent proteins

机译:应用表达两种荧光蛋白的诱导型腺病毒载体后背根神经节神经元线粒体成像

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摘要

Mitochondrial morphology and dynamics are known to vary considerably depending on the cell type and organism studied. The objective of this study was to assess the potential application of adenoviral-fluorescent protein constructs for long-term tracking of mitochondria in neurons. An adenoviral vector containing two fluorescent proteins, the enhanced green fluorescent protein (eGFP) targeted to the cyto-plasm to highlight the neuronal processes, and the red fluorescent protein (RFP) directed to mitochondria under the control of an inducible promoter, facilitated an efficient and accurate method to study mitochondrial dynamics in long-term studies. Dorsal root ganglion neurons from rat embryos were cultured and infected. The infected neurons exhibited green fluorescence after 24 h, while 16 h following induction with doxycycline, red fluorescence protein began to localize within mitochondria. The red fluorescent protein was transported into mitochondria at the cell body followed by distribution within processes. As the neurons aged, the expression of red fluorescent protein was confined to cytoplasmic vacuoles and not mitochondria. Further analysis suggested that the cytoplasmic vacuoles were likely of lysosomal origin. Taken together, the current study presents novel strategies to study the life history of cellular organelles such as mitochondria in long-term studies.
机译:已知线粒体的形态和动力学会因所研究的细胞类型和生物体而有很大差异。这项研究的目的是评估腺病毒荧光蛋白构建体在长期跟踪神经元线粒体中的潜在应用。包含两种荧光蛋白的腺病毒载体,靶向细胞质以突出神经元过程的增强型绿色荧光蛋白(eGFP),以及在诱导型启动子控制下的针对线粒体的红色荧光蛋白(RFP)促进了高效长期研究线粒体动力学的精确方法。培养并感染来自大鼠胚胎的背根神经节神经元。被感染的神经元在24小时后呈现绿色荧光,而在强力霉素诱导后16小时,红色荧光蛋白开始定位于线粒体内。红色荧光蛋白被转运到细胞体的线粒体中,然后在过程中分布。随着神经元的衰老,红色荧光蛋白的表达局限于细胞质液泡而不是线粒体。进一步的分析表明,胞浆液泡可能是溶酶体来源的。综上所述,当前的研究提出了新颖的策略,以长期研究细胞线粒体等细胞器的生命史。

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