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In vivo metabolic imaging of insulin with multiphoton fluorescence of human insulin-Au nanodots

机译:人胰岛素-Au纳米点多光子荧光对胰岛素的体内代谢成像

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摘要

Functional human insulin-Au nanodots (NDs) are synthesized for the in vivo imaging of insulin metabolism. Benefiting from its efficient red to near infrared fluorescence, deep tissue subcellular uptake of insulin-Au NDs can be clearly resolved through a least-invasive harmonic generation and two-photon fluorescence (TPF) microscope. In vivo investigations on mice ear and ex vivo assays on human fat tissues conclude that cells with rich insulin receptors have higher uptake of administrated insulin. Interestingly, the insulin-Au NDs can even permeate into lipid droplets (LDs) of adipocytes. Using this newly discovered metabolic phenomenon of insulin, it is found that enlarged adipocytes in type II diabetes mice have higher adjacent/LD concentration contrast with small-sized ones in wild type mice. For human clinical samples, the epicardial adipocytes of patients with diabetes and coronary artery disease (CAD) also show elevated adjacent/LD concentration contrast. As a result, human insulin-Au nanodots provide a new approach to explore subcellular insulin metabolism in model animals or patients with metabolic or cardiovascular diseases.
机译:合成功能性人胰岛素-Au纳米点(ND),用于胰岛素代谢的体内成像。得益于其高效的红色至近红外荧光,可通过微创谐波产生和双光子荧光(TPF)显微镜清楚地解决胰岛素-Au ND的深层组织亚细胞吸收。在小鼠耳朵上进行的体内研究以及对人体脂肪组织的离体测定得出的结论是,具有丰富胰岛素受体的细胞对胰岛素的吸收更高。有趣的是,胰岛素-Au ND甚至可以渗透到脂肪细胞的脂滴(LDs)中。利用这种新发现的胰岛素代谢现象,发现与野生型小鼠中的小脂肪细胞相比,II型糖尿病小鼠中的脂肪细胞增大具有更高的邻近/ LD浓度。对于人类临床样品,患有糖尿病和冠状动脉疾病(CAD)的患者的心外膜脂肪细胞也显示出升高的邻近/ LD浓度对比。结果,人胰岛素-Au纳米点提供了一种探索模型动物或患有代谢或心血管疾病的患者中亚细胞胰岛素代谢的新方法。

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