Honda Teruko, Inagawa Hiroyuki
Department of Medical Technology, School of Life and Environmental Science, Azabu University, Kanagawa, Japan
Research Institute for Healthy Living, Niigata University of Pharmacy and Applied Life Sciences, Niigata, Japan.
Anticancer Res. 2019 Aug;39(8):4475-4478. doi: 10.21873/anticanres.13621.
Chronic inflammation is involved in the development of cancer, lifestyle-related diseases, and autoimmune diseases. It also influences the severity of these diseases. Macrophages that accumulate in tumor tissues and adipose tissues of obesity have been shown to increase expression of inflammatory cytokines, thereby inducing inflammatory changes in these tissues. The macrophage phenotype is believed to be important in mediating inflammatory changes in tissues. Recently, monocytes/macrophages activated with low-dose lipopolysaccharide (LPS) were demonstrated to suppress increased expression of monocyte chemotactic protein (MCP)-1 and inflammatory cytokines (interleukin (IL)-1 β, IL-8, and tumor necrosis factor (TNF)-α). By suppressing the increased expression of chemotaxis-related and inflammation-related factors, monocytes/macrophages activated with low-dose LPS are considered to suppress the migration of macrophages into tissues and to regulate inflammatory changes in these tissues, respectively. The effects of macrophages activated with low-dose LPS were different from those of macrophages activated with high-dose LPS. In this review, we discuss the usefulness of monocytes/macrophages activation by low-dose LPS.
慢性炎症与癌症、生活方式相关疾病及自身免疫性疾病的发生发展有关。它还会影响这些疾病的严重程度。已证实,在肿瘤组织和肥胖症患者脂肪组织中积聚的巨噬细胞会增加炎性细胞因子的表达,从而在这些组织中引发炎症变化。巨噬细胞表型被认为在介导组织炎症变化中起重要作用。最近,有研究表明,用低剂量脂多糖(LPS)激活的单核细胞/巨噬细胞可抑制单核细胞趋化蛋白(MCP)-1和炎性细胞因子(白细胞介素(IL)-1β、IL-8和肿瘤坏死因子(TNF)-α)的表达增加。通过抑制趋化相关因子和炎症相关因子的表达增加,用低剂量LPS激活的单核细胞/巨噬细胞被认为可分别抑制巨噬细胞向组织的迁移并调节这些组织中的炎症变化。低剂量LPS激活的巨噬细胞的作用与高剂量LPS激活的巨噬细胞的作用不同。在本综述中,我们讨论了低剂量LPS激活单核细胞/巨噬细胞的作用。