A critical role for MSR1 in vesicular stomatitis virus infection of the central nervous system
Summary: 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 stom...
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doaj-68148bd3715249fda8d5abe7355ab89d2021-06-27T04:39:36ZengElsevieriScience2589-00422021-06-01246102678A critical role for MSR1 in vesicular stomatitis virus infection of the central nervous systemDuomeng Yang0Tao Lin1Cen Li2Andrew G. Harrison3Tingting Geng4Penghua Wang5Department of Immunology, School of Medicine, University of Connecticut Health Center, Farmington, CT 06030, USADepartment of Immunology, School of Medicine, University of Connecticut Health Center, Farmington, CT 06030, USADepartment of Microbiology & Immunology, School of Medicine, New York Medical College, Valhalla, NY 10595, USADepartment of Immunology, School of Medicine, University of Connecticut Health Center, Farmington, CT 06030, USADepartment of Immunology, School of Medicine, University of Connecticut Health Center, Farmington, CT 06030, USADepartment of Immunology, School of Medicine, University of Connecticut Health Center, Farmington, CT 06030, USA; Corresponding authorSummary: 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 (Msr1−/−) 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 Msr1+/− 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.http://www.sciencedirect.com/science/article/pii/S2589004221006465Molecular physiologyNeuroscienceVirologyCell biology |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Duomeng Yang Tao Lin Cen Li Andrew G. Harrison Tingting Geng Penghua Wang |
spellingShingle |
Duomeng Yang Tao Lin Cen Li Andrew G. Harrison Tingting Geng Penghua Wang A critical role for MSR1 in vesicular stomatitis virus infection of the central nervous system iScience Molecular physiology Neuroscience Virology Cell biology |
author_facet |
Duomeng Yang Tao Lin Cen Li Andrew G. Harrison Tingting Geng Penghua Wang |
author_sort |
Duomeng Yang |
title |
A critical role for MSR1 in vesicular stomatitis virus infection of the central nervous system |
title_short |
A critical role for MSR1 in vesicular stomatitis virus infection of the central nervous system |
title_full |
A critical role for MSR1 in vesicular stomatitis virus infection of the central nervous system |
title_fullStr |
A critical role for MSR1 in vesicular stomatitis virus infection of the central nervous system |
title_full_unstemmed |
A critical role for MSR1 in vesicular stomatitis virus infection of the central nervous system |
title_sort |
critical role for msr1 in vesicular stomatitis virus infection of the central nervous system |
publisher |
Elsevier |
series |
iScience |
issn |
2589-0042 |
publishDate |
2021-06-01 |
description |
Summary: 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 (Msr1−/−) 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 Msr1+/− 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. |
topic |
Molecular physiology Neuroscience Virology Cell biology |
url |
http://www.sciencedirect.com/science/article/pii/S2589004221006465 |
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