自体荧光
CD3型
CD28
CD8型
T细胞
分子生物学
化学
细胞生物学
生物
免疫学
免疫系统
抗原
荧光
物理
光学
作者
Alex J. Walsh,Katherine P. Mueller,Kelsey Tweed,Isabel Jones,Christine M. Walsh,Nicole J. Piscopo,Natalie M. Niemi,David J. Pagliarini,Krishanu Saha,Melissa C. Skala
标识
DOI:10.1038/s41551-020-0592-z
摘要
The function of a T cell depends on its subtype and activation state. Here, we show that imaging of the autofluorescence lifetime signals of quiescent and activated T cells can be used to classify the cells. T cells isolated from human peripheral blood and activated in culture using tetrameric antibodies against the surface ligands CD2, CD3 and CD28 showed specific activation-state-dependent patterns of autofluorescence lifetime. Logistic regression models and random forest models classified T cells according to activation state with 97-99% accuracy, and according to activation state (quiescent or activated) and subtype (CD3+CD8+ or CD3+CD4+) with 97% accuracy. Autofluorescence lifetime imaging can be used to non-destructively determine T-cell function.
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