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Intracellular dynamics of the gene delivery vehicle polyethylenimine during transfection: investigation by two-photon fluorescence correlation spectroscopy

机译:转染过程中基因传递载体聚乙烯亚胺的细胞内动力学:通过双光子荧光相关光谱法研究

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Though polyethylenimine (PEI) is one of the most efficient nonviral vectors, one concern is the significant cytotoxicity of free PEI that represents about 80% of the PEI molecules in PEI/DNA mixtures used for transfection. In this respect, the aim of this work was to further investigate the intracellular fate of PEI during transfection of L929 fibroblasts. To this end, we analyzed by fluorescence correlation spectroscopy (FCS) using two-photon excitation the intracellular concentration and diffusion properties of labeled PEI and PEI/DNA complexes in various compartments of L929 cells. High initial fluorescence intensity, rapid photobleaching and the absence of measurable autocorrelation curves in most selected locations in cytoplasm suggest that PEI/DNA complexes and PEI accumulate (up to 30 times the concentration in the extracellular medium) in late endosomes bound to the inner membrane face. This feature, together with membrane destabilizing properties of PEI, may explain the release of PEI into cytoplasm and subsequent diffusion into the nucleus. In the nucleus, the concentration of PEI was found to be about 2.5- to 3.5-fold higher than the one in the incubation medium. Moreover, autocorrelation curves obtained in the nuclear compartment can be analyzed with either a two-component model (with the major fraction undergoing free Brownian diffusion) or an anomalous diffusion model. Both the endosomal disruption and the large intranuclear PEI concentration may contribute to PEI cytotoxicity.
机译:尽管聚乙烯亚胺(PEI)是最有效的非病毒载体之一,但人们关注的是游离PEI的明显细胞毒性,该游离PEI代表用于转染的PEI / DNA混合物中PEI分子的约80%。在这方面,这项工作的目的是进一步研究在转染L929成纤维细胞过程中PEI的细胞内命运。为此,我们使用双光子激发,通过荧光相关光谱法(FCS)分析了L929细胞各个区室中标记的PEI和PEI / DNA复合物的细胞内浓度和扩散特性。高初始荧光强度,快速的光致漂白和在细胞质中大多数选定位置缺乏可测量的自相关曲线,表明PEI / DNA复合物和PEI在结合于内膜表面的晚期内体中积聚(最高达细胞外培养基浓度的30倍)。 。该特征以及PEI的膜不稳定特性可以解释PEI释放到细胞质中以及随后扩散到细胞核中的原因。在细胞核中,发现PEI的浓度比孵育培养基中的浓度高约2.5至3.5倍。此外,在核室中获得的自相关曲线可以用两组分模型(主要部分进行自由布朗扩散)或异常扩散模型进行分析。内体破坏和大的核内PEI浓度均可能导致PEI细胞毒性。

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