A Quantitative Multivariate Model of Human Dendritic Cell-T Helper Cell Communication

被引:21
|
作者
Grandclaudon, Maximilien [1 ,2 ]
Perrot-Dockes, Marie [3 ]
Trichot, Coline [1 ,2 ]
Karpf, Lea [1 ,2 ]
Abouzid, Omar [1 ,2 ]
Chauvin, Camille [1 ,2 ]
Sirven, Philemon [1 ,2 ]
Abou-Jaoude, Wassim [4 ]
Berger, Frederique [1 ,5 ,6 ]
Hupe, Philippe [1 ,6 ,7 ]
Thieffry, Denis [4 ]
Sansonnet, Laure [3 ]
Chiquet, Julien [3 ]
Levy-Leduc, Celine [3 ]
Soumelis, Vassili [1 ,2 ]
机构
[1] PSL Res Univ, Ctr Rech, Inst Curie, F-75005 Paris, France
[2] INSERM, U932, Immun & Canc, F-75005 Paris, France
[3] Univ Paris Saclay, INRA, AgroParisTech, UMR MIA Paris, F-75005 Paris, France
[4] PSL Univ, CNRS, INSERM,UMR8197,U1024, Ecole Normale Super,Inst Biol,Computat Syst Biol, F-75005 Paris, France
[5] PSL Res Univ, Inst Curie, Unit Biostat, F-75005 Paris, France
[6] PSL Res Univ, Inst Curie, INSERM, U900, F-75005 Paris, France
[7] Mines Paris Tech, F-77305 Fontainebleau, France
关键词
GROWTH-FACTOR-BETA; REGULATORY NETWORK; DIFFERENTIATION; STIMULATION; PLASTICITY; SELECTION; LINEAGE; HEALTH;
D O I
10.1016/j.cell.2019.09.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell-cell communication involves a large number of molecular signals that function as words of a complex language whose grammar remains mostly unknown. Here, we describe an integrative approach involving (1) protein-level measurement of multiple communication signals coupled to output responses in receiving cells and (2) mathematical modeling to uncover input-output relationships and interactions between signals. Using human dendritic cell (DC)-T helper (Th) cell communication as a model, we measured 36 DC-derived signals and 17Th cytokines broadly covering Th diversity in 428 observations. We developed a data-driven, computationally validated model capturing 56 already described and 290 potentially novel mechanisms of Th cell specification. By predicting context-dependent behaviors, we demonstrate a new function for IL-12p70 as an inducer of Th17 in an IL-1 signaling context. This work provides a unique resource to decipher the complex combinatorial rules governing DC-Th cell communication and guide their manipulation for vaccine design and immunotherapies.
引用
收藏
页码:432 / +
页数:37
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