脂质代谢
诱导多能干细胞
细胞
电池类型
代谢途径
细胞生物学
细胞培养
生物
脂滴
荧光寿命成像显微镜
新陈代谢
计算生物学
化学
生物化学
胚胎干细胞
荧光
基因
遗传学
量子力学
物理
作者
Yeran Bai,Carolina M. Camargo,Stella M.K. Glasauer,Raymond Gifford,Xinran Tian,Andrew P. Longhini,Kenneth S. Kosik
标识
DOI:10.1038/s41467-023-44675-0
摘要
Abstract Understanding metabolic heterogeneity is the key to uncovering the underlying mechanisms of metabolic-related diseases. Current metabolic imaging studies suffer from limitations including low resolution and specificity, and the model systems utilized often lack human relevance. Here, we present a single-cell metabolic imaging platform to enable direct imaging of lipid metabolism with high specificity in various human-derived 2D and 3D culture systems. Through the incorporation of an azide-tagged infrared probe, selective detection of newly synthesized lipids in cells and tissue became possible, while simultaneous fluorescence imaging enabled cell-type identification in complex tissues. In proof-of-concept experiments, newly synthesized lipids were directly visualized in human-relevant model systems among different cell types, mutation status, differentiation stages, and over time. We identified upregulated lipid metabolism in progranulin-knockdown human induced pluripotent stem cells and in their differentiated microglia cells. Furthermore, we observed that neurons in brain organoids exhibited a significantly lower lipid metabolism compared to astrocytes.
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