Division of Biology, Kansas State University, KS 66506, USA.
Cell Biochem Funct. 2010 Dec 2;28(8):686-94. doi: 10.1002/cbf.1709.
Helicobacter species are common laboratory pathogens which induce intestinal inflammation and disease in susceptible mice. Since in vitro studies indicate that Helicobacter products activate macrophages, we hypothesized that in vivo Helicobacter infection regulates the inflammatory response of intestinal muscularis macrophages from C57Bl/6 mice. Helicobacter hepaticus infection increased surface expression of macrophage markers F4/80, CD11b and MHC-II within whole intestinal muscle mounts. However, constitutive cytokine and chemokine production by macrophages isolated from infected mice significantly decreased compared to macrophages from uninfected mice despite no detectable bacterial products in the cultures. In addition, muscularis macrophages from infected mice up-regulated FIZZ-1 and SK-1 gene expression, suggesting the macrophages had an anti-inflammatory phenotype. Corresponding with increased anti-inflammatory gene expression, macrophages from infected mice were more phagocytic but did not produce cytokines after stimulation with LPS and IFN-γ or immune complexes and IL-4. Therefore, the presence of Helicobacter infection matures intestinal muscularis macrophages, modulating the constitutive macrophage response to become more anti-inflammatory and resistant to secondary stimulation.
幽门螺旋杆菌是常见的实验室病原体,可在易感小鼠中引起肠道炎症和疾病。由于体外研究表明幽门螺旋杆菌产物能激活巨噬细胞,我们假设体内幽门螺旋杆菌感染可调节 C57Bl/6 小鼠肠道肌层巨噬细胞的炎症反应。肝螺杆菌感染增加了整个肠道肌层中巨噬细胞标志物 F4/80、CD11b 和 MHC-II 的表面表达。然而,与未感染的小鼠相比,尽管培养物中未检测到细菌产物,但从感染小鼠中分离出的巨噬细胞的固有细胞因子和趋化因子的产生显著减少。此外,感染小鼠的肌层巨噬细胞上调了 FIZZ-1 和 SK-1 基因的表达,表明巨噬细胞具有抗炎表型。与抗炎基因表达增加相对应,感染小鼠的巨噬细胞吞噬作用增强,但在用 LPS 和 IFN-γ 或免疫复合物和 IL-4 刺激后不产生细胞因子。因此,幽门螺旋杆菌感染的存在使肠道肌层巨噬细胞成熟,调节固有巨噬细胞反应,使其更具抗炎性和对二次刺激的抵抗力。