Dual Feedforward Loops Modulate Type I Interferon Responses and Induce Selective Gene Expression during TLR4 Activation

被引:8
作者
Zhou, Jie [1 ]
Sun, Tingzhe [2 ]
Jin, Shouheng [1 ]
Guo, Zhiyong [3 ]
Cui, Jun [1 ]
机构
[1] Sun Yat Sen Univ, MOE Key Lab Gene Funct & Regulat, State Key Lab Biocontrol, Sch Life Sci, Guangzhou 510006, Guangdong, Peoples R China
[2] Anqing Normal Univ, Sch Life Sci, Anqing 246011, Anhui, Peoples R China
[3] Sun Yat Sen Univ, Organ Transplant Ctr, Affiliated Hosp 1, Guangzhou 510080, Peoples R China
基金
中国国家自然科学基金;
关键词
TOLL-LIKE RECEPTORS; NEGATIVE FEEDBACK; TEMPORAL CONTROL; NETWORK MOTIFS; DYNAMICS; OSCILLATIONS; RECOGNITION; SPECIFICITY; ROLES; TRAF3;
D O I
10.1016/j.isci.2020.100881
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
Although the dynamic features of type I coherent feedforward loop (C1-FFL) has been well studied, how C1-FFL shapes cell-to-cell heterogeneity remains unclear. Here, we found that C1-FFL with OR logic serves as "noise reducer," whereas C1-FFL with AND logic functions as "noise propagator" to fine-tune the heterogeneity of signaling molecule's activation. Within Toll-like receptor 4 (TLR4) signaling pathway, we demonstrated that MyD88 together with TRIF generates a C1-FFL to control TBK1 phosphorylation and reduce its cell-to-cell heterogeneity, whereas noisy TRIF activation induced high heterogeneity of IRF3 activation through another C1-FF L. We further developed a mathematical model with dual C1-FFLs to uncover how MyD88 and TRIF encoded differential dynamics for TBK1 and IRF3 activation. Integration of dual FFLs drives MyD88-TBK1 axis to determine the specificity of IFN-stimulated genes transcription. Collectively, our work elucidates a paradigm that tunable TLR4-mediated type I IFN responses are subtly controlled by dual FFLs.
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页数:32
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