Section of Molecular Biology, Division of Biological Sciences, University of California, San Diego, La Jolla, United States.
Department of Bioengineering, University of California, San Diego, La Jolla, United States.
Elife. 2020 Sep 18;9:e58825. doi: 10.7554/eLife.58825.
Cells use molecular circuits to interpret and respond to extracellular cues, such as hormones and cytokines, which are often released in a temporally varying fashion. In this study, we combine microfluidics, time-lapse microscopy, and computational modeling to investigate how the type I interferon (IFN)-responsive regulatory network operates in single human cells to process repetitive IFN stimulation. We found that IFN-α pretreatments lead to opposite effects, priming versus desensitization, depending on input durations. These effects are governed by a regulatory network composed of a fast-acting positive feedback loop and a delayed negative feedback loop, mediated by upregulation of ubiquitin-specific peptidase 18 (USP18). We further revealed that USP18 upregulation can only be initiated at the G1/early S phases of cell cycle upon the treatment onset, resulting in heterogeneous and delayed induction kinetics in single cells. This cell cycle gating provides a temporal compartmentalization of feedback loops, enabling duration-dependent desensitization to repetitive stimulations.
细胞利用分子电路来解释和响应细胞外信号,如激素和细胞因子,这些信号通常以时间变化的方式释放。在这项研究中,我们结合微流控、延时显微镜和计算建模来研究 I 型干扰素(IFN)反应性调节网络如何在单个人类细胞中运作以处理重复的 IFN 刺激。我们发现,IFN-α 预处理会根据输入持续时间产生相反的效果,即引发和脱敏。这些效应由一个由快速作用的正反馈回路和延迟的负反馈回路组成的调节网络控制,该网络由泛素特异性肽酶 18(USP18)的上调介导。我们进一步揭示,USP18 的上调只能在处理开始时在细胞周期的 G1/早期 S 期启动,导致单个细胞中存在异质和延迟的诱导动力学。这种细胞周期门控为反馈回路提供了时间分隔,使细胞能够对重复刺激产生持续时间依赖性脱敏。