Lu Yong, Biancotto Angelique, Cheung Foo, Remmers Elaine, Shah Naisha, McCoy J Philip, Tsang John S
Systems Genomics and Bioinformatics Unit, Laboratory of Systems Biology, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD 20892, USA.
Trans-NIH Center for Human Immunology, Autoimmunity, and Inflammation, NIH, Bethesda, MD 20892, USA.
Immunity. 2016 Nov 15;45(5):1162-1175. doi: 10.1016/j.immuni.2016.10.025.
Cell-to-cell expression variation (CEV) is a prevalent feature of even well-defined cell populations, but its functions, particularly at the organismal level, are not well understood. Using single-cell data obtained via high-dimensional flow cytometry of T cells as a model, we introduce an analysis framework for quantifying CEV in primary cell populations and studying its functional associations in human cohorts. Analyses of 840 CEV phenotypes spanning multiple baseline measurements of 14 proteins in 28 T cell subpopulations suggest that the quantitative extent of CEV can exhibit substantial subject-to-subject differences and yet remain stable within healthy individuals over months. We linked CEV to age and disease-associated genetic polymorphisms, thus implicating CEV as a biomarker of aging and disease susceptibility and suggesting that it might play an important role in health and disease. Our dataset, interactive figures, and software for computing CEV with flow cytometry data provide a resource for exploring CEV functions.
细胞间表达变异(CEV)是即使定义明确的细胞群体也普遍存在的一个特征,但其功能,尤其是在生物体水平上的功能,尚未得到充分了解。以通过T细胞的高维流式细胞术获得的单细胞数据为模型,我们引入了一个分析框架,用于量化原代细胞群体中的CEV,并研究其在人类队列中的功能关联。对28个T细胞亚群中14种蛋白质的多个基线测量的840种CEV表型进行分析表明,CEV的定量程度在个体之间可能存在显著差异,但在健康个体中数月内仍保持稳定。我们将CEV与年龄和疾病相关的基因多态性联系起来,从而表明CEV是衰老和疾病易感性的生物标志物,并暗示它可能在健康和疾病中发挥重要作用。我们的数据集、交互式图表以及用于通过流式细胞术数据计算CEV的软件为探索CEV功能提供了资源。