Spent Coffee Ground-Derived Carbon Dots as Redox-Modulating Biomaterials for Astrocytic Differentiation of Human Neural Progenitor Cells

氧化应激 活性氧 细胞生物学 细胞内 祖细胞 神经干细胞 生物相容性 材料科学 下调和上调 抗氧化剂 细胞分化 化学 氧化磷酸化 生物物理学 生物化学 纳米技术 纳米材料 细胞 干细胞 细胞培养 细胞生长 细胞凋亡 生物材料
作者
Ji Hee Kim,Hyun Myung Doo,Kyuna Park,Ah Young Lee,Hongki Kim,Sung Ho Song,Chi Kyung Kim,Jin‐Heong Yim,Jong Seob Choi
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:18 (34): 45971-45986
标识
DOI:10.1021/acsami.6c05623
摘要

Food waste-derived carbon dots (CDs) from spent coffee grounds or spinach were synthesized via hydrothermal and solvothermal methods and systematically characterized for their photoluminescence and surface chemical properties. Biological evaluations using human neural progenitor cells (hNPCs) demonstrated efficient cellular uptake and high biocompatibility across all synthesized CDs. Notably, coffee-derived blue-emitting CDs (B-CDs) exhibited robust concentration-dependent antioxidant activity and reduced intracellular reactive oxygen species (ROS) levels. In addition, B-CDs were associated with enhanced astrocytic differentiation of hNPCs. To further evaluate the antioxidative effects of B-CDs under oxidative stress conditions, cells were exposed to H2O2-induced oxidative stress during differentiation. B-CDs alleviated oxidative stress-associated cellular damage and reduced the expression of inflammation-related markers. This antioxidative effect was accompanied by the downregulation of C3, a marker of neurotoxic reactive astrocytes. Further, B-CDs promoted early phosphorylation of STAT3 (Tyr705), a key driver of astrocytic differentiation, and induced sustained expression of a cytoprotective enzyme HO-1, linking intracellular ROS reduction to astrocyte-biased differentiation. This work demonstrates that food waste-derived CDs can function as bioactive nanomaterials capable of modulating neural progenitor cell differentiation and mitigating cellular stress. These findings highlight their potential for applications in neural interface materials, regenerative medicine, and redox-responsive biomaterial systems.

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