Poole Jill A, Anderson Leigh, Gleason Angela M, West William W, Romberger Debra J, Wyatt Todd A
Pulmonary, Critical Care, Sleep & Allergy Division, Department of Internal Medicine .
J Immunotoxicol. 2015 Jan-Mar;12(1):64-73. doi: 10.3109/1547691X.2014.882449. Epub 2014 Feb 3.
Exposure to agriculture organic dusts, comprised of a diversity of pathogen-associated molecular patterns, results in chronic airway diseases. The multi-functional class A macrophage scavenger receptor (SRA)/CD204 has emerged as an important class of pattern recognition receptors with broad ligand binding ability. The objective was to determine the role of SRA in mediating repetitive and post-inflammatory organic dust extract (ODE)-induced airway inflammation. Wild-type (WT) and SRA knockout (KO) mice were intra-nasally treated with ODE or saline daily for 3 weeks and immediately euthanized or allowed to recover for 1 week. Results show that lung histopathologic changes were increased in SRA KO mice as compared to WT following repetitive ODE exposures marked predominately by increased size and distribution of lymphoid aggregates. After a 1-week recovery from daily ODE treatments, there was significant resolution of lung injury in WT mice, but not SRA KO animals. The increased lung histopathology induced by ODE treatment was associated with decreased accumulation of neutrophils, but greater accumulation of CD4(+) T-cells. The lung cytokine milieu induced by ODE was consistent with a TH1/TH17 polarization in both WT and SRA KO mice. Overall, the data demonstrate that SRA/CD204 plays an important role in the normative inflammatory lung response to ODE, as evidenced by the enhanced dust-mediated injury viewed in the absence of this receptor.
接触由多种病原体相关分子模式组成的农业有机粉尘会导致慢性气道疾病。多功能A类巨噬细胞清道夫受体(SRA)/CD204已成为一类重要的模式识别受体,具有广泛的配体结合能力。目的是确定SRA在介导重复性和炎症后有机粉尘提取物(ODE)诱导的气道炎症中的作用。野生型(WT)和SRA基因敲除(KO)小鼠每天经鼻给予ODE或生理盐水,持续3周,然后立即安乐死或恢复1周。结果显示,与WT小鼠相比,SRA KO小鼠在重复性ODE暴露后肺组织病理学变化增加,主要表现为淋巴聚集物的大小和分布增加。在每天给予ODE治疗1周后恢复,WT小鼠的肺损伤有明显缓解,但SRA KO动物没有。ODE治疗引起的肺组织病理学增加与中性粒细胞积累减少有关,但CD4(+) T细胞积累增加。ODE诱导的肺细胞因子环境在WT和SRA KO小鼠中均与TH1/TH17极化一致。总体而言,数据表明SRA/CD204在对ODE的正常炎症性肺反应中起重要作用,这在缺乏该受体时观察到的增强的粉尘介导损伤中得到证明。