败血症
C5a受体
先天免疫系统
免疫学
受体
补体系统
趋化性
免疫印迹
中性粒细胞胞外陷阱
炎症
生物
内化
获得性免疫系统
医学
免疫系统
内科学
生物化学
基因
作者
Renfeng Guo,Niels C. Riedemann,Kurt D. Bernacki,Vidya Sarma,Ines J. Laudes,Jayne S. Reuben,Ellen M. Younkin,Thomas A. Neff,Joseph Paulauskis,Firas S. Zetoune,Peter A. Ward
标识
DOI:10.1096/fj.03-0009fje
摘要
Complement fragment 5a (C5a)–C5a receptor (C5aR) signaling plays an essential role in neutrophil innate immunity. Blockade of either the ligand or the receptor improves survival rates in experimental sepsis. In the current study, sepsis was induced in rats by cecal ligation/puncture. Early in sepsis C5aR content on neutrophils significantly dropped, reached the nadir at 24 h after onset of sepsis, and progressively elevated thereafter. Western‐blot, RT‐PCR, and confocal microscopy analyses revealed that the loss and re‐expression of C5aR during sepsis might be due, at least in part, to the receptor internalization and reconstitution. The reduction and reconstitution of C5aR correlate with the loss and restoration of innate immune functions of blood neutrophils (chemotaxis and reactive oxygen species production), respectively. Quantitative measurements of C5aR on blood neutrophils are highly predictive of survival or death during sepsis. These data suggest that neutrophil C5aR content represents an essential component of an efficient defense system in sepsis and may serve as a prognostic marker for the outcome.
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