Palmer Megan J, Mahajan Vinay S, Trajman Lily C, Irvine Darrell J, Lauffenburger Douglas A, Chen Jianzhu
Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Cell Mol Immunol. 2008 Apr;5(2):79-89. doi: 10.1038/cmi.2008.10.
Interleukin-7 (IL-7) is an essential cytokine for the development and homeostatic maintenance of T and B lymphocytes. Binding of IL-7 to its cognate receptor, the IL-7 receptor (IL-7R), activates multiple pathways that regulate lymphocyte survival, glucose uptake, proliferation and differentiation. There has been much interest in understanding how IL-7 receptor signaling is modulated at multiple interconnected network levels. This review examines how the strength of the signal through the IL-7 receptor is modulated in T and B cells, including the use of shared receptor components, signaling crosstalk, shared interaction domains, feedback loops, integrated gene regulation, multimerization and ligand competition. We discuss how these network control mechanisms could integrate to govern the properties of IL-7R signaling in lymphocytes in health and disease. Analysis of IL-7 receptor signaling at a network level in a systematic manner will allow for a comprehensive approach to understanding the impact of multiple signaling pathways on lymphocyte biology.
白细胞介素-7(IL-7)是T和B淋巴细胞发育及稳态维持所必需的细胞因子。IL-7与其同源受体白细胞介素-7受体(IL-7R)结合,可激活多种调节淋巴细胞存活、葡萄糖摄取、增殖和分化的信号通路。人们对了解IL-7受体信号在多个相互关联的网络层面如何被调节非常感兴趣。本综述探讨了T细胞和B细胞中通过IL-7受体的信号强度是如何被调节的,包括共享受体成分的使用、信号串扰、共享相互作用结构域、反馈回路、整合基因调控、多聚化和配体竞争。我们讨论了这些网络控制机制如何整合以在健康和疾病状态下调控淋巴细胞中IL-7R信号的特性。以系统的方式在网络层面分析IL-7受体信号,将有助于全面理解多种信号通路对淋巴细胞生物学的影响。