In vitro Infection of Primary Human Monocytes with HIV-1
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O'Connell, Patrick
[1
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Zheng, Yong-Hui
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Michigan State Univ, Coll Osteopath Med, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USAMichigan State Univ, Coll Osteopath Med, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USA
Zheng, Yong-Hui
[1
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Amalfitano, Andrea
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Michigan State Univ, Coll Osteopath Med, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USA
Michigan State Univ, Coll Osteopath Med, Dept Pediat, E Lansing, MI 48824 USAMichigan State Univ, Coll Osteopath Med, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USA
Amalfitano, Andrea
[1
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Aldhamen, Yasser A.
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Michigan State Univ, Coll Osteopath Med, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USAMichigan State Univ, Coll Osteopath Med, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USA
Aldhamen, Yasser A.
[1
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[1] Michigan State Univ, Coll Osteopath Med, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USA
[2] Michigan State Univ, Coll Osteopath Med, Dept Pediat, E Lansing, MI 48824 USA
Monocyte infection by HIV-1 is an important component of chronic HIV pathogenesis. Following infection by HIV-1, monocytes are able to cross the blood brain barrier and set up a viral reservoir in the central nervous system. Additionally, in the setting of chronic HIV-1 infection, monocytes can become activated either directly through HIV-1 infection or indirectly via HIV-1-mediated systemic immune activation. Currently, there are few studies looking at HIV-1 infection of primary human monocytes in vitro. Furthermore, detection of successful HIV-1 infection of monocytes can be laborious requiring an ELISA for p24 or assessing levels of HIV-1 mRNA or DNA. This protocol utilizes an HIV-1 strain expressing GFP to allow for easy quantification of HIV-1 infection by fluorescence-assisted cell sorting (FACS). By determining HIV-1 infection by FACS one can take advantage of its multiparametric nature allowing for the use of less cells and the ability to assess the expression of other markers on HIV-1(+) and HIV-1(-) cells in the same experiment. Additionally, this protocol could be modified to study HIV-1 infection of other cells including CD4(+) T cells.