Fei Fei, Qu Jie, Li Chunyuan, Wang Xinlu, Li Yuwei, Zhang Shiwu
Nankai University School of Medicine, Nankai University, Tianjin, 300071 People's Republic of China.
Departments of Pathology, Tianjin Union Medical Center, Tianjin, 300121 People's Republic of China.
Cell Biosci. 2017 Nov 25;7:64. doi: 10.1186/s13578-017-0191-1. eCollection 2017.
S100A4, an important member of the S100 family of proteins, is best known for its significant role in promoting cancer progression and metastasis. In addition to its expression in tumors, upregulation of S100A4 expression has been associated with various non-tumor pathophysiology processes. However, the mechanisms underlying the role of S100A4 remain unclear. Activated "host" cells (fibroblasts, immunocytes, vascular cells, among others) secrete S100A4 into the extracellular space in various non-tumor human disorders, where it executes its biological functions by interacting with intracellular target proteins. However, the exact molecular mechanisms underlying these interactions in different non-tumor pathophysiologies vary, and S100A4 is likely one of the cross-linking factors that acts as common intrinsic constituents of biological mechanisms. Numerous studies have indicated that the S100A4-mediated epithelial-mesenchymal transition plays a vital role in the occurrence and development of various non-tumor pathophysiologies. Epithelial-mesenchymal transition can be categorized into three general subtypes based on the phenotype and function of the output cells. S100A4 regulates tissue fibrosis associated with the type II epithelial-mesenchymal transition via various signaling pathways. Additionally, S100A4 stimulates fibroblasts to secrete fibronectin and collagen, thus forming the structural components of the extracellular matrix (ECM) and stimulating their deposition in tissues, contributing to the formation of a pro-inflammatory niche. Simultaneously, S100A4 enhances the motility of macrophages, neutrophils, and leukocytes and promotes the recruitment and chemotaxis of these inflammatory cells to regulate inflammation and immune functions. S100A4 also exerts a neuroprotective pro-survival effect on neurons by rescuing them from brain injury and participates in angiogenesis by interacting with other target molecules. In this review, we summarize the role of S100A4 in fibrosis, inflammation, immune response, neuroprotection, angiogenesis, and some common non-tumor diseases as well as its possible involvement in molecular pathways and potential clinical value.
S100A4是S100蛋白家族的重要成员,因其在促进癌症进展和转移中发挥的重要作用而最为人所知。除了在肿瘤中的表达外,S100A4表达上调还与多种非肿瘤病理生理过程相关。然而,S100A4发挥作用的潜在机制仍不清楚。在各种非肿瘤性人类疾病中,活化的“宿主”细胞(成纤维细胞、免疫细胞、血管细胞等)将S100A4分泌到细胞外空间,在那里它通过与细胞内靶蛋白相互作用来执行其生物学功能。然而,这些相互作用在不同非肿瘤病理生理学中的具体分子机制各不相同,S100A4可能是作为生物学机制共同内在成分的交联因子之一。大量研究表明,S100A4介导的上皮-间质转化在各种非肿瘤病理生理学的发生和发展中起着至关重要的作用。上皮-间质转化可根据输出细胞的表型和功能分为三种一般亚型。S100A4通过各种信号通路调节与II型上皮-间质转化相关的组织纤维化。此外,S100A4刺激成纤维细胞分泌纤连蛋白和胶原蛋白,从而形成细胞外基质(ECM)的结构成分并刺激它们在组织中的沉积,有助于促炎微环境的形成。同时,S100A4增强巨噬细胞、中性粒细胞和白细胞的运动性,并促进这些炎症细胞的募集和趋化作用,以调节炎症和免疫功能。S100A4还通过使神经元免受脑损伤对其发挥神经保护的促存活作用,并通过与其他靶分子相互作用参与血管生成。在本综述中,我们总结了S100A4在纤维化、炎症、免疫反应、神经保护、血管生成以及一些常见非肿瘤疾病中的作用,以及其可能参与的分子途径和潜在临床价值。