Depletion and reconstitution of macrophages in mice with vesicular stomatitis virus infection
Acting as the first line of host defense, macrophages play a central role in antiviral response. Here, we present a protocol for depletion and reconstitution of macrophages in mice with vesicular stomatitis virus (VSV) infection. We describe steps for induction and isolation of peritoneal macrophage...
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Veröffentlicht in: | STAR protocols 2023-06, Vol.4 (2), p.102319-102319, Article 102319 |
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Sprache: | eng |
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Zusammenfassung: | Acting as the first line of host defense, macrophages play a central role in antiviral response. Here, we present a protocol for depletion and reconstitution of macrophages in mice with vesicular stomatitis virus (VSV) infection. We describe steps for induction and isolation of peritoneal macrophages from CD45.2+ donor mice, macrophage depletion in CD45.1+ recipient mice, adoptive transfer of CD45.2+ macrophages to CD45.1+ recipient mice, and VSV infection. This protocol highlights the role of exogenous macrophages in antiviral response in vivo.
For complete details on the use and execution of this profile, please refer to Wang et al.1
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•Vesicular stomatitis virus amplification and titration•Induction and isolation of peritoneal macrophages•Macrophage depletion and adoptive transfer•In vivo VSV infection
Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics.
Acting as the first line of host defense, macrophages play a central role in antiviral response. Here, we present a protocol for depletion and reconstitution of macrophages in mice with vesicular stomatitis virus (VSV) infection. We describe steps for induction and isolation of peritoneal macrophages from CD45.2+ donor mice, macrophage depletion in CD45.1+ recipient mice, adoptive transfer of CD45.2+ macrophages to CD45.1+ recipient mice, and VSV infection. This protocol highlights the role of exogenous macrophages in antiviral response in vivo. |
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ISSN: | 2666-1667 2666-1667 |
DOI: | 10.1016/j.xpro.2023.102319 |