Yang Duomeng, Lin Tao, Li Cen, Harrison Andrew G, Geng Tingting, Wang Penghua
Department of Immunology, School of Medicine, University of Connecticut Health Center, Farmington, CT 06030, USA.
Department of Microbiology & Immunology, School of Medicine, New York Medical College, Valhalla, NY 10595, USA.
iScience. 2021 Jun 1;24(6):102678. doi: 10.1016/j.isci.2021.102678. eCollection 2021 Jun 25.
Macrophage scavenger receptor 1 (MSR1) plays an important role in host defense to bacterial infections, M2 macrophage polarization, and lipid homeostasis. However, its physiological function in viral pathogenesis remains poorly defined. Herein, we report that MSR1 facilitates vesicular stomatitis virus (VSV) infection in the central nervous system. Msr1-deficient ( ) mice presented reduced morbidity, mortality, and viral loads in the spinal cord following lethal VSV infection, along with normal viremia and innate immune responses, compared to littermates and wild-type mice. Msr1 expression was most significantly upregulated in the spinal cord, the predominant target of VSV. Mechanistically, through its extracellular domains, MSR1 interacted with VSV surface glycoprotein and facilitated its cellular entry in a low-density lipoprotein receptor-dependent manner. In conclusion, our results demonstrate that MSR1 serves as a cofactor for VSV cellular entry and facilitates its infection preferentially in the spinal cord.
巨噬细胞清道夫受体1(MSR1)在宿主抵御细菌感染、M2巨噬细胞极化和脂质稳态中发挥重要作用。然而,其在病毒发病机制中的生理功能仍不清楚。在此,我们报告MSR1促进水疱性口炎病毒(VSV)在中枢神经系统中的感染。与同窝小鼠和野生型小鼠相比,Msr1基因敲除()小鼠在感染致死剂量的VSV后,发病率、死亡率降低,脊髓中的病毒载量减少,同时病毒血症和固有免疫反应正常。MSR1的表达在VSV的主要靶器官脊髓中上调最为显著。机制上,MSR1通过其细胞外结构域与VSV表面糖蛋白相互作用,并以低密度脂蛋白受体依赖的方式促进其进入细胞。总之,我们的结果表明,MSR1作为VSV进入细胞的辅助因子,优先促进其在脊髓中的感染。