Departamento de Farmacobiología, Centro de Investigación y de Estudios Avanzados (Cinvestav), Unidad Sede Sur. Calzada de los Tenorios No. 235, Col. Granjas Coapa, Mexico City 14330, Mexico.
Cells. 2020 Nov 4;9(11):2411. doi: 10.3390/cells9112411.
Mast cells (MCs) constitute an essential cell lineage that participates in innate and adaptive immune responses and whose phenotype and function are influenced by tissue-specific conditions. Their mechanisms of activation in type I hypersensitivity reactions have been the subject of multiple studies, but the signaling pathways behind their activation by innate immunity stimuli are not so well described. Here, we review the recent evidence regarding the main molecular elements and signaling pathways connecting the innate immune receptors and hypoxic microenvironment to cytokine synthesis and the secretion of soluble or exosome-contained mediators in this cell type. When known, the positive and negative control mechanisms of those pathways are presented, together with their possible implications for the understanding of mast cell-driven chronic inflammation. Finally, we discuss the relevance of the knowledge about signaling in this cell type in the recognition of MCs as central elements on innate immunity, whose remarkable plasticity converts them in sensors of micro-environmental discontinuities and controllers of tissue homeostasis.
肥大细胞(MCs)构成了一个重要的细胞谱系,参与先天和适应性免疫反应,其表型和功能受组织特异性条件的影响。它们在 I 型超敏反应中的激活机制已经是多项研究的主题,但它们被先天免疫刺激物激活的信号通路还没有得到很好的描述。在这里,我们回顾了最近关于连接先天免疫受体和缺氧微环境与细胞因子合成以及该细胞类型中可溶性或外泌体包含的介质分泌的主要分子元件和信号通路的主要证据。当已知时,呈现了这些途径的正、负控制机制,以及它们对理解肥大细胞驱动的慢性炎症的可能影响。最后,我们讨论了关于该细胞类型信号的知识在识别 MCs 作为先天免疫的核心要素中的相关性,其显著的可塑性使它们成为微环境不连续性的传感器和组织动态平衡的控制器。