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Activation of cell signaling via optical manipulation of gold-coated liposomes encapsulating signaling molecules

机译:通过包封信号分子的金包被脂质体的光学操作激活细胞信号

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Many diseases involve changes in cell signaling cascades, as seen commonly in drug resistant cancers. To better understand these intricate signaling events in diseased cells and tissues, experimental methods of probing cellular communication at a single to multi-cell level are required. We recently introduced a general platform for activation of selected signaling pathways by optically controlled delivery and release of water soluble factors using gold-coated liposomes. In the example presented here, we encapsulated inositol trisphosphate (IP3), a ubiquitous intracellular secondary messenger involved in GPCR and Akt signaling cascades, within 100 nm gold-coated liposomes. The high polarizability of the liposome's unique gold pseudo-shell allows stable optical trapping for subcellular manipulation in the presence of cells. We take this optical manipulation further by optically injecting IP3-containing liposomes into the cytosol of a single cell to initiate localized cell signaling. Upon optical injection of liposomal IP3 into a single ovarian carcinoma cell, we observed localized activation as reported by changes in Indo-1 fluorescence intensity. With established gap junctions between the injected cell and neighboring cells, we monitored propagation of this signaling to and through nearby cells.
机译:如在抗药性癌症中常见的那样,许多疾病涉及细胞信号传导级联的改变。为了更好地了解患病细胞和组织中这些复杂的信号事件,需要在单细胞或多细胞水平上探测细胞通讯的实验方法。我们最近介绍了一个通用平台,该平台可使用包金的脂质体通过光学控制的传递和释放水溶性因子来激活选定的信号通路。在此处显示的示例中,我们将肌醇三磷酸酯(IP3)(一种参与GPCR和Akt信号传导级联的无处不在的细胞内二级信使)封装在100 nm镀金脂质体中。脂质体独特的金假壳的高极化性允许在存在细胞的情况下进行亚细胞操作的稳定光学捕获。我们通过将含IP3的脂质体光学注射到单个细胞的胞质溶胶中以启动局部细胞信号传导,从而进一步进行这种光学操作。将脂质体IP3光学注射到单个卵巢癌细胞中后,我们观察到局部激活,如Indo-1荧光强度的变化所报道。通过在注入的细胞和相邻细胞之间建立间隙连接,我们监测了该信号传导至附近细胞并通过附近细胞的传播。

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