肽聚糖
先天免疫系统
TLR2型
微生物学
生物
CD14型
Toll样受体
TLR4型
细菌细胞结构
肺炎链球菌
模式识别受体
免疫系统
金黄色葡萄球菌
脂多糖
革兰氏阴性菌
细菌
免疫学
大肠杆菌
抗生素
生物化学
基因
遗传学
作者
Atsutoshi Yoshimura,Egil Lien,Robin R. Ingalls,Elaine Tuomanen,Roman Dziarski,Douglas T. Golenbock
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:1999-07-01
卷期号:163 (1): 1-5
被引量:1257
标识
DOI:10.4049/jimmunol.163.1.1
摘要
Abstract Invasive infection with Gram-positive and Gram-negative bacteria often results in septic shock and death. The basis for the earliest steps in innate immune response to Gram-positive bacterial infection is poorly understood. The LPS component of the Gram-negative bacterial cell wall appears to activate cells via CD14 and Toll-like receptor (TLR) 2 and TLR4. We hypothesized that Gram-positive bacteria might also be recognized by TLRs. Heterologous expression of human TLR2, but not TLR4, in fibroblasts conferred responsiveness to Staphylococcus aureus and Streptococcus pneumoniae as evidenced by inducible translocation of NF-κB. CD14 coexpression synergistically enhanced TLR2-mediated activation. To determine which components of Gram-positive cell walls activate Toll proteins, we tested a soluble preparation of peptidoglycan prepared from S. aureus. Soluble peptidoglycan substituted for whole organisms. These data suggest that the similarity of clinical response to invasive infection by Gram-positive and Gram-negative bacteria is due to bacterial recognition via similar TLRs.
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