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Intracellular light-induced release of signaling molecules from gold-coated liposomes

机译:细胞内光诱导信号从包金的脂质体中释放

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The combination of laser light and composite nanovesicles enables unique opportunities for precise delivery to, and on-demand release of molecular compounds within, single cells at high spatiotemporal resolution. Here, we demonstrate precise delivery and intracellular release of molecules from gold-coated liposomes via near infrared (NIR) light. The plasmon resonant gold shell provides a light-sensitive trigger for on-demand content release from thermosensitive liposomes. Two demonstrations of intracellular delivery and release from gold-coated liposomes are presented here. The first example uses microinjection to preload gold-coated liposomes into a single cell, followed by exposure to on-resonant NIR laser light to trigger release of a fluorescent nuclear dye intracellularly. In the second delivery and release demonstration, gold-coated liposomes encapsulating inositol trisphosphate (IP3), a ubiquitous secondary messenger in cell signaling cascades, passively accumulate within cells via endocytosis. Exposure to on-resonant MR laser wavelength of light induces rapid release of IP3 from the intracellular liposomes and subsequent activation of Ca~(2+) signaling at a single cell, monitored by changes in fluorescence intensity of a Ca~(2+)-sensitive dye.
机译:激光和复合纳米囊泡的组合为在高时空分辨率下精确递送到单细胞内以及按需释放分子化合物提供了独特的机会。在这里,我们展示了通过近红外(NIR)光从镀金脂质体中精确递送和分子内释放分子的过程。等离子体共振金壳为从热敏脂质体释放按需内容提供了光敏触发。这里展示了金包膜脂质体的细胞内递送和释放的两个证明。第一个例子是使用显微注射将包金的脂质体预装到单个细胞中,然后暴露于共振NIR激光中以触发细胞内荧光核染料的释放。在第二次传递和释放演示中,包封肌醇三磷酸(IP3)(细胞信号级联中无处不在的次级信使)的金包衣脂质体通过内吞作用被动积累在细胞内。暴露于共振MR激光波长的光可诱导IP3从细胞内脂质体快速释放并随后在单个细胞中激活Ca〜(2+)信号,并通过Ca〜(2 +)-的荧光强度变化进行监测敏感染料。

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