Xu Jintao, Flaczyk Adam, Neal Lori M, Fa Zhenzong, Eastman Alison J, Malachowski Antoni N, Cheng Daphne, Moore Bethany B, Curtis Jeffrey L, Osterholzer John J, Olszewski Michal A
Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, University of Michigan Health System, Ann Arbor, MI 48109.
Pulmonary Section, Medical Service, VA Ann Arbor Healthcare System, Department of Veterans Affairs Health System, Ann Arbor, MI 48105; and.
J Immunol. 2017 May 1;198(9):3548-3557. doi: 10.4049/jimmunol.1700057. Epub 2017 Mar 15.
The scavenger receptor macrophage receptor with collagenous structure (MARCO) promotes protective innate immunity against bacterial and parasitic infections; however, its role in host immunity against fungal pathogens, including the major human opportunistic fungal pathogen , remains unknown. Using a mouse model of infection, we demonstrated that MARCO deficiency leads to impaired fungal control during the afferent phase of cryptococcal infection. Diminished fungal containment in MARCO mice was accompanied by impaired recruitment of Ly6C monocytes and monocyte-derived dendritic cells (moDC) and lower moDC costimulatory maturation. The reduced recruitment and activation of mononuclear phagocytes in MARCO mice was linked to diminished early expression of IFN-γ along with profound suppression of CCL2 and CCL7 chemokines, providing evidence for roles of MARCO in activation of the CCR2 axis during infection. Lastly, we found that MARCO was involved in phagocytosis by resident pulmonary macrophages and DC. We conclude that MARCO facilitates early interactions between and lung-resident cells and promotes the production of CCR2 ligands. In turn, this contributes to a more robust recruitment and activation of moDC that opposes rapid fungal expansion during the afferent phase of cryptococcal infection.
具有胶原结构的清道夫受体巨噬细胞受体(MARCO)可促进针对细菌和寄生虫感染的保护性固有免疫;然而,其在宿主抗真菌病原体免疫中的作用,包括针对主要的人类机会性真菌病原体的作用,仍不清楚。利用新型隐球菌感染的小鼠模型,我们证明了MARCO缺陷会导致新型隐球菌感染传入阶段的真菌控制受损。MARCO基因敲除小鼠中真菌抑制能力的减弱伴随着Ly6C单核细胞和单核细胞来源的树突状细胞(moDC)募集受损以及moDC共刺激成熟度降低。MARCO基因敲除小鼠中单核吞噬细胞募集和激活的减少与IFN-γ早期表达的减少以及CCL2和CCL7趋化因子的显著抑制有关,这为MARCO在新型隐球菌感染过程中激活CCR2轴的作用提供了证据。最后,我们发现MARCO参与了驻留肺巨噬细胞和树突状细胞对新型隐球菌的吞噬作用。我们得出结论,MARCO促进了新型隐球菌与肺驻留细胞之间的早期相互作用,并促进了CCR2配体的产生。反过来,这有助于更有力地募集和激活moDC,从而在新型隐球菌感染的传入阶段对抗真菌的快速扩散。