期刊
JOURNAL OF CELL BIOLOGY
卷 177, 期 2, 页码 329-341出版社
ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.200609050
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资金
- Medical Research Council [MC_U122663296, MC_U122665002, U.1226.00.003.00001.01(65002)] Funding Source: Medline
- NIAID NIH HHS [R01 AI049784, AI-49784] Funding Source: Medline
- MRC [MC_U122663296, MC_U122665002] Funding Source: UKRI
- Medical Research Council [MC_U122663296, MC_U122665002] Funding Source: researchfish
In macrophages, HIV-1 has been shown to bud into intracellular structures that contain the late endosome marker CD63. We show that these organelles are not endosomes, but an internally sequestered plasma membrane domain. Using immunofluorescence microscopy and immunoelectron microscopy, we find that HIV-1 buds into a compartment that contains the tetraspanins CD81, CD9, and CD53. On uninfected macrophages, these proteins are seen at the cell surface and in intracellular vacuole-like structures with a complex content of vesicles and interconnected membranes that lack endosome markers, including CD63. Significantly, these structures are accessible to small tracers (horseradish peroxidase or ruthenium red) applied to cells at 4 degrees C, indicating that they are connected to the cell surface. HIV assembles on, and accumulates within, these intracellular compartments. Furthermore, CD63 is recruited to the virus-containing structures and incorporated into virions. These results indicate that, in macrophages, HIV-1 exploits a previously undescribed intracellular plasma membrane domain to assemble infectious particles.
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