Single-cell spatial metabolomics with cell-type specific protein profiling for tissue systems biology

被引:38
|
作者
Hu, Thomas [1 ,2 ,3 ]
Allam, Mayar [1 ,2 ]
Cai, Shuangyi [1 ,2 ]
Henderson, Walter [4 ]
Yueh, Brian [5 ]
Garipcan, Aybuke [5 ]
Ievlev, Anton V. [6 ]
Afkarian, Maryam [7 ]
Beyaz, Semir [5 ]
Coskun, Ahmet F. [1 ,2 ,8 ,9 ,10 ]
机构
[1] Georgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30322 USA
[2] Emory Univ, Atlanta, GA USA
[3] Georgia Inst Technol, Sch Elect & Comp Engn, Atlanta, GA USA
[4] Inst Elect & Nanotechnol, Georgia Inst Technol, Atlanta, GA USA
[5] Cold Spring Harbor Lab, Cold Spring Harbor, NY USA
[6] Ctr Nanophase Mat Sci, Oak Ridge Natl Lab, Oak Ridge, TN USA
[7] Univ Calif Davis, Dept Internal Med, Div Nephrol, Davis, CA USA
[8] Georgia Inst Technol, Interdisciplinary Bioengn Grad Program, Atlanta, GA 30322 USA
[9] Emory Univ, Winship Canc Inst, Atlanta, GA 30322 USA
[10] Georgia Inst Technol, Parker H Petit Inst Bioengn & Biosci, Atlanta, GA 30332 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
GERMINAL CENTER; B-CELLS; CANCER; CENTERS; METABOLISM; SELECTION; LIGHT; DARK; FAT;
D O I
10.1038/s41467-023-43917-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Metabolic reprogramming in cancer and immune cells occurs to support their increasing energy needs in biological tissues. Here we propose Single Cell Spatially resolved Metabolic (scSpaMet) framework for joint protein-metabolite profiling of single immune and cancer cells in male human tissues by incorporating untargeted spatial metabolomics and targeted multiplexed protein imaging in a single pipeline. We utilized the scSpaMet to profile cell types and spatial metabolomic maps of 19507, 31156, and 8215 single cells in human lung cancer, tonsil, and endometrium tissues, respectively. The scSpaMet analysis revealed cell type-dependent metabolite profiles and local metabolite competition of neighboring single cells in human tissues. Deep learning-based joint embedding revealed unique metabolite states within cell types. Trajectory inference showed metabolic patterns along cell differentiation paths. Here we show scSpaMet's ability to quantify and visualize the cell-type specific and spatially resolved metabolic-protein mapping as an emerging tool for systems-level understanding of tissue biology. The authors developed a framework for joint protein-metabolite profiling at the single-cell level in human tissue combining targeted multiplexed protein imaging and untargeted spatial metabolomics in a single pipeline.
引用
收藏
页数:20
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