Macropinosomes are a site of HIV-1 entry into primary CD4 <sup>+</sup> T cells
Abstract
HIV-1 has been observed to enter target cells at both the plasma membrane and endosomes. However, which pathways mediate its entry into primary CD4 + T cells, the major targets of this virus, remains unclear. Here, we show that HIV-1 can enter primary CD4 + T cells through macropinocytosis, a form of endocytosis. We found that HIV-1 can enter primary CD4 + T cells at both the plasma membrane and internal compartments, while entry into common T cell lines occurred primarily at the plasma membrane. Inhibition of macropinocytosis suppressed HIV-1 internalization into and subsequent fusion with primary CD4 + T cells regardless of the viral coreceptor usage. Microscopic analysis of viral contents exposed to the cytosol confirmed that HIV-1 fusion occurs at the macropinosomal membrane. Finally, the inhibition of macropinocytosis blocked HIV-1 infection of primary CD4 + T cells. Altogether, this study identifies macropinocytosis as one pathway for HIV-1 entry into primary CD4 + T cells.
Article Details
Journal Info
Proceedings of the National Academy of Sciences
National Academy of Sciences
Authors (10)
Tomoyuki Murakami
Department of Microbiology & Immunology, University of Michigan Medical School
Ricardo de Souza Cardoso
Department of Microbiology & Immunology, University of Michigan Medical School
Praveen Manivannan
Department of Microbiology & Immunology, University of Michigan Medical School
Ya-Ting Chang
Eric Rentchler
Microscopy core, Biomedical Research Core Facilities, Office of Research, University of Michigan Medical School
Kai-Neng Chou
Department of Microbiology & Immunology, University of Michigan Medical School
Yipei Tang
Department of Microbiology & Immunology, University of Michigan Medical School
Joel A. Swanson
Department of Microbiology & Immunology, University of Michigan Medical School
Philip D. King
Department of Microbiology & Immunology, University of Michigan Medical School
Akira Ono
Department of Microbiology & Immunology, University of Michigan Medical School