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赖氨酸和 DAP 型肽聚糖均不能通过 Toll 样受体 2 激活小鼠或人固有免疫细胞。

Neither Lys- and DAP-type peptidoglycans stimulate mouse or human innate immune cells via Toll-like receptor 2.

机构信息

The Oklahoma Medical Research Foundation, Program in Arthritis & Immunology, Oklahoma City, OK, United States of America.

The Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States of America.

出版信息

PLoS One. 2018 Feb 23;13(2):e0193207. doi: 10.1371/journal.pone.0193207. eCollection 2018.

Abstract

Peptidoglycan (PGN), a major component of bacterial cell walls, is a pathogen-associated molecular pattern (PAMP) that causes innate immune cells to produce inflammatory cytokines that escalate the host response during infection. In order to better understand the role of PGN in infection, we wanted to gain insight into the cellular receptor for PGN. Although the receptor was initially identified as Toll-like receptor 2 (TLR2), this receptor has remained controversial and other PGN receptors have been reported. We produced PGN from live cultures of Bacillus anthracis and Staphylococcus aureus and tested samples of PGN isolated during the purification process to determine at what point TLR2 activity was removed, if at all. Our results indicate that although live B. anthracis and S. aureus express abundant TLR2 ligands, highly-purified PGN from either bacterial source is not recognized by TLR2.

摘要

肽聚糖 (PGN) 是细菌细胞壁的主要成分,是一种病原体相关的分子模式 (PAMP),可导致先天免疫细胞产生炎症细胞因子,从而在感染过程中加剧宿主反应。为了更好地了解 PGN 在感染中的作用,我们希望深入了解 PGN 的细胞受体。尽管该受体最初被鉴定为 Toll 样受体 2 (TLR2),但该受体一直存在争议,并且已经报道了其他 PGN 受体。我们从活的炭疽芽孢杆菌和金黄色葡萄球菌培养物中产生 PGN,并测试了在纯化过程中分离的 PGN 样本,以确定 TLR2 活性是否被去除,如果有的话。我们的结果表明,尽管活的炭疽芽孢杆菌和金黄色葡萄球菌表达丰富的 TLR2 配体,但来自任何一种细菌来源的高度纯化的 PGN 都不能被 TLR2 识别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/feb4/5825070/8dc206c1a2ea/pone.0193207.g001.jpg

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