趋化因子
促炎细胞因子
TLR4型
刺激
细胞因子
受体
免疫学
生物
人口
巨噬细胞炎性蛋白
Toll样受体
TLR9型
炎症
医学
免疫系统
内分泌学
先天免疫系统
基因表达
生物化学
基因
DNA甲基化
环境卫生
作者
Stanislas Grassin‐Delyle,Charlotte Abrial,Hélène Salvator,Marion Brollo,Emmanuel Naline,Philippe Devillier
摘要
<b><i>Background:</i></b> The Toll-like receptor (TLR) family is involved in the recognition of and response to microbial infections. These receptors are expressed in leukocytes. TLR stimulation induces the production of proinflammatory cytokines and chemokines. Given that human lung macrophages (LMs) constitute the first line of defense against inhaled pathogens, the objective of this study was to investigate the expression and function of TLR subtypes in this cell population. <b><i>Methods:</i></b> Human primary LMs were obtained from patients undergoing surgical resection. The RNA and protein expression levels of TLRs, chemokines, and cytokines were assessed after incubation with subtype-selective agonists. <b><i>Results:</i></b> In human LMs, the TLR expression level varied from one subtype to another. Stimulation with subtype-selective agonists induced an intense, concentration- and time-dependent increase in the production of chemokines and cytokines. TLR4 stimulation induced the strongest effect, whereas TLR9 stimulation induced a much weaker response. <b><i>Conclusions:</i></b> The stimulation of TLRs in human LMs induces intense cytokine and chemokine production, a characteristic of the proinflammatory M1 macrophage phenotype.
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