发布: 2016年10月05日第6卷第19期 DOI: 10.21769/BioProtoc.1945 浏览次数: 10759
评审: Ivan ZanoniAchille BroggiMarco Di Gioia
Abstract
Bacterial lipopolysaccharide (LPS) is present in the outer membrane of Gram-negative bacteria and functions as pathogen-associated molecular pattern (PAMP) (Whitfield and Trent, 2014). LPS therefore is a potent activator of inflammatory responses leading to cytokine release and neutrophils recruitment. The lipid A moiety of LPS activates the complex consisting of the LPS binding protein (LBP), CD14, MD-2 and Toll-like receptor 4 (TLR4) and the non-canonical inflammasome-linked caspases-4, 5 and 11, which in turn activate the canonical NLRP3 inflammasome (Shi et al., 2014; Hagar et al., 2013; Kayagaki et al., 2013; Hoshino et al., 1999; Poltorak, 1998; Nagai et al., 2002; Park et al., 2009; Ratsimandresy et al., 2013). In particular, the cytokine interleukin (IL)-1β produced in response to inflammasome activation has a crucial role in neutrophil recruitment through promoting neutrophil adhesion and migration (McDonald et al., 2010).This protocol allows studying of inflammatory response induced by LPS that affect neutrophil infiltration by tracking myeloperoxidase (MPO) activity in vivo (de Almeida et al., 2015).
Keywords: Inflammation (炎症)Materials and Reagents
Equipment
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Procedure
文章信息
版权信息
© 2016 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
de Almeida, L., Dorfleutner, A. and Stehlik, C. (2016). In vivo Analysis of Neutrophil Infiltration during LPS-induced Peritonitis. Bio-protocol 6(19): e1945. DOI: 10.21769/BioProtoc.1945.
分类
免疫学 > 动物模型 > 小鼠
细胞生物学 > 细胞运动 > 细胞迁移
细胞生物学 > 细胞信号传导 > 胁迫反应
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