The interaction network between group 3 innate lymphoid cells and other cells

IF 6.3 3区 综合性期刊 Q1 Multidisciplinary Fundamental Research Pub Date : 2025-11-01 Epub Date: 2023-12-30 DOI:10.1016/j.fmre.2023.10.021
Yi-tong Hu , Xing-zi Liu , Yue-miao Zhang , Xiaohuan Guo
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Abstract

Group 3 innate lymphoid cells (ILC3s) have emerged as significant regulators of tissue homeostasis, immunity and inflammation through various effector molecules in response to signals within the tissue microenvironment. Multiple signals derived from the tissue microenvironment have been illustrated in recent years, which could either activate or suppress the activity of ILC3s. ILC3s, in turn, could also influence many other cells through their effector molecules, such as interleukin (IL)-22, IL-17 and lymphotoxins, indicating that ILC3s act as an important hub in the complex network of cell interactions. In this review, we discuss our current appreciation of the functional crosstalk between ILC3s and myeloid cells, T and B cells, epithelial cells or other types of cells, thus highlighting the emerging importance of communication between these cells for the prevention or induction of relevant diseases and providing insights for future directions of investigation and therapeutic interventions.
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第 3 组先天性淋巴细胞与其他细胞之间的相互作用网络
第3组先天淋巴样细胞(ILC3s)已成为组织稳态、免疫和炎症的重要调节因子,通过各种效应分子响应组织微环境中的信号。近年来,来自组织微环境的多种信号被证明可以激活或抑制ILC3s的活性。反过来,ILC3s也可以通过其效应分子影响许多其他细胞,如白细胞介素(IL)-22、IL-17和淋巴毒素,这表明ILC3s在细胞相互作用的复杂网络中起着重要的枢纽作用。在这篇综述中,我们讨论了我们目前对ILC3s与骨髓细胞、T细胞和B细胞、上皮细胞或其他类型细胞之间的功能串扰的认识,从而强调了这些细胞之间的通信对预防或诱导相关疾病的重要性,并为未来的研究方向和治疗干预提供了见解。
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来源期刊
Fundamental Research
Fundamental Research Multidisciplinary-Multidisciplinary
CiteScore
4.00
自引率
1.60%
发文量
294
审稿时长
79 days
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