Munford Robert S
Molecular Host Defense Laboratory, Departments of Internal Medicine and Microbiology, University of Texas Southwestern Medical School, Dallas, Texas 75390, USA.
J Endotoxin Res. 2005;11(2):69-84. doi: 10.1179/096805105X35161.
Animals that cannot sense endotoxin may die if they are infected by Gram-negative bacteria. Animals that sense endotoxin and respond too vigorously may also die, victims of their own inflammatory reactions. The outcome of Gram-negative bacterial infection is thus determined not only by an individual's ability to sense endotoxin and respond to its presence, but also by numerous phenomena that inactivate endotoxin and/or prevent harmful reactions to it. Endotoxin sensing requires the MD-2/TLR4 recognition complex and occurs principally in local tissues and the liver. This review highlights the known detoxification mechanisms, which include: (i) proteins that facilitate LPS sequestration by plasma lipoproteins, prevent interactions between the bioactive lipid A moiety and MD-2/TLR4, or promote cellular uptake via non-signaling pathway(s); (ii) enzymes that deacylate or dephosphorylate lipid A; (iii) mechanisms that remove LPS and Gram-negative bacteria from the bloodstream; and (iv) neuroendocrine adaptations that modulate LPS-induced mediator production or neutralize pro-inflammatory molecules in the circulation. In general, the mechanisms for sensing and detoxifying endotoxin seem to be compartmentalized (local versus systemic), dynamic, and variable between individuals. They may have evolved to confine infection and inflammation to extravascular sites of infection while preventing harmful systemic reactions. Integration of endotoxin sensing and detoxification is essential for successful host defense.
无法感知内毒素的动物如果感染革兰氏阴性菌可能会死亡。能够感知内毒素并产生过度强烈反应的动物也可能死亡,成为自身炎症反应的牺牲品。因此,革兰氏阴性菌感染的结果不仅取决于个体感知内毒素并对其存在做出反应的能力,还取决于许多使内毒素失活和/或防止对其产生有害反应的现象。内毒素感知需要MD-2/TLR4识别复合物,主要发生在局部组织和肝脏中。本综述重点介绍了已知的解毒机制,包括:(i)促进血浆脂蛋白隔离LPS、防止生物活性脂质A部分与MD-2/TLR4相互作用或通过非信号通路促进细胞摄取的蛋白质;(ii)使脂质A脱酰基或去磷酸化的酶;(iii)从血液中清除LPS和革兰氏阴性菌的机制;以及(iv)调节LPS诱导的介质产生或中和循环中促炎分子的神经内分泌适应性变化。一般来说,内毒素感知和解毒机制似乎是分隔的(局部与全身)、动态的,且个体之间存在差异。它们可能已经进化到将感染和炎症限制在血管外感染部位,同时防止有害的全身反应。内毒素感知和解毒的整合对于成功的宿主防御至关重要。