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Graphene quantum dots as universal fluorophores and their use in revealing regulated trafficking of insulin receptors in adipocytes

机译:石墨烯量子点作为通用荧光团及其在揭示脂肪细胞中胰岛素受体调节运输的应用

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Graphene quantum dots (GQDs) hold great promise as a new class of fluorophores for bioimaging, owing to their remarkable physicochemical properties including tunable photoluminescence, excellent photostability, and biocompatibility. Despite their highly anticipated potentials, GQDs have yet to be used to specifically label and track molecular targets involved in dynamic cellular processes in live cells. Here, we demonstrate that GQDs can serve as universal fluorophores for bioimaging because they can be readily conjugated with a wide range of biomolecules while preserving their functionalities. As a proof-of-concept demonstration, insulin-conjugated GQDs have been synthesized and utilized for specific labeling and dynamic tracking of insulin receptors in 3T3-L1 adipocytes. Our experiments reveal, for the first time, that the internalization and recycling of insulin receptors in adipocytes are oppositely regulated by apelin and TNFα, which may contribute to the regulations of these two cytokines in insulin sensitivity.
机译:石墨烯量子点(GQD)由于其显着的理化特性(包括可调光致发光,出色的光稳定性和生物相容性)而作为一种新型的生物成像荧光剂具有广阔的前景。尽管具有很高的潜力,但GQD尚未用于特异性标记和跟踪活细胞中动态细胞过程涉及的分子靶标。在这里,我们证明GQD可以用作生物成像的通用荧光团,因为它们可以很容易地与各种生物分子结合,同时保留其功能。作为概念证明,已合成了胰岛素偶联的GQD,并将其用于3T3-L1脂肪细胞中胰岛素受体的特异性标记和动态跟踪。我们的实验首次揭示,脂肪细胞中胰岛素受体的内在化和再循环受apelin和TNFα的相反调控,这可能有助于调节这两种细胞因子对胰岛素的敏感性。

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