Rietschel E T, Schletter J, Weidemann B, El-Samalouti V, Mattern T, Zähringer U, Seydel U, Brade H, Flad H D, Kusumoto S, Gupta D, Dziarski R, Ulmer A J
Research Center Borstel, Center for Medicine and Biosciences, Germany.
Microb Drug Resist. 1998 Spring;4(1):37-44. doi: 10.1089/mdr.1998.4.37.
Surface structures of bacteria contribute to the microbial pathogenic potential and are capable of causing local and generalized inflammatory reactions. Among these factors, endotoxin and peptidoglycan are of particular medical importance. Both toxic bacterial polymers are now recognized to interact with the same cellular receptor, the CD14 molecule, which is expressed on different types of immune cells, in particular, monocytes/macrophages. The interaction between these bacterial activators and CD14 leads to the production of endogenous mediators such as tumor necrosis factor alpha, interleukin 1 (IL-1), and IL-6, which are ultimately responsible for phlogistic responses. The fact that CD14 recognizes not only endotoxin and peptidoglycan but also other glycosyl-based microbial polymers suggests that this cellular surface molecule represents a lectin.
细菌的表面结构有助于微生物的致病潜力,并能够引发局部和全身性炎症反应。在这些因素中,内毒素和肽聚糖具有特别重要的医学意义。现在已经认识到,这两种有毒细菌聚合物都与相同的细胞受体即CD14分子相互作用,CD14分子在不同类型的免疫细胞尤其是单核细胞/巨噬细胞上表达。这些细菌激活剂与CD14之间的相互作用会导致内源性介质如肿瘤坏死因子α、白细胞介素1(IL-1)和IL-6的产生,这些介质最终导致炎症反应。CD14不仅能识别内毒素和肽聚糖,还能识别其他基于糖基的微生物聚合物,这一事实表明这种细胞表面分子代表一种凝集素。