HIV-1 buds predominantly at the plasma membrane of primary human macrophages.

HIV-1 assembly and release are believed to occur at the plasma membrane in most host cells with the exception of primary macrophages, for which exclusive budding at late endosomes has been reported. Here, we applied a novel ultrastructural approach to assess HIV-1 budding in primary macrophages in a...

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Main Authors: Sonja Welsch, Oliver T Keppler, Anja Habermann, Ina Allespach, Jacomine Krijnse-Locker, Hans-Georg Kräusslich
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2007-03-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC1829407?pdf=render
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spelling doaj-dae3efd0d20448eca167e705a23ab2f52020-11-25T01:35:06ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742007-03-0133e3610.1371/journal.ppat.0030036HIV-1 buds predominantly at the plasma membrane of primary human macrophages.Sonja WelschOliver T KepplerAnja HabermannIna AllespachJacomine Krijnse-LockerHans-Georg KräusslichHIV-1 assembly and release are believed to occur at the plasma membrane in most host cells with the exception of primary macrophages, for which exclusive budding at late endosomes has been reported. Here, we applied a novel ultrastructural approach to assess HIV-1 budding in primary macrophages in an immunomarker-independent manner. Infected macrophages were fed with BSA-gold and stained with the membrane-impermeant dye ruthenium red to identify endosomes and the plasma membrane, respectively. Virus-filled vacuolar structures with a seemingly intracellular localization displayed intense staining with ruthenium red, but lacked endocytosed BSA-gold, defining them as plasma membrane. Moreover, HIV budding profiles were virtually excluded from gold-filled endosomes while frequently being detected on ruthenium red-positive membranes. The composition of cellular marker proteins incorporated into HIV-1 supported a plasma membrane-derived origin of the viral envelope. Thus, contrary to current opinion, the plasma membrane is the primary site of HIV-1 budding also in infected macrophages.http://europepmc.org/articles/PMC1829407?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Sonja Welsch
Oliver T Keppler
Anja Habermann
Ina Allespach
Jacomine Krijnse-Locker
Hans-Georg Kräusslich
spellingShingle Sonja Welsch
Oliver T Keppler
Anja Habermann
Ina Allespach
Jacomine Krijnse-Locker
Hans-Georg Kräusslich
HIV-1 buds predominantly at the plasma membrane of primary human macrophages.
PLoS Pathogens
author_facet Sonja Welsch
Oliver T Keppler
Anja Habermann
Ina Allespach
Jacomine Krijnse-Locker
Hans-Georg Kräusslich
author_sort Sonja Welsch
title HIV-1 buds predominantly at the plasma membrane of primary human macrophages.
title_short HIV-1 buds predominantly at the plasma membrane of primary human macrophages.
title_full HIV-1 buds predominantly at the plasma membrane of primary human macrophages.
title_fullStr HIV-1 buds predominantly at the plasma membrane of primary human macrophages.
title_full_unstemmed HIV-1 buds predominantly at the plasma membrane of primary human macrophages.
title_sort hiv-1 buds predominantly at the plasma membrane of primary human macrophages.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2007-03-01
description HIV-1 assembly and release are believed to occur at the plasma membrane in most host cells with the exception of primary macrophages, for which exclusive budding at late endosomes has been reported. Here, we applied a novel ultrastructural approach to assess HIV-1 budding in primary macrophages in an immunomarker-independent manner. Infected macrophages were fed with BSA-gold and stained with the membrane-impermeant dye ruthenium red to identify endosomes and the plasma membrane, respectively. Virus-filled vacuolar structures with a seemingly intracellular localization displayed intense staining with ruthenium red, but lacked endocytosed BSA-gold, defining them as plasma membrane. Moreover, HIV budding profiles were virtually excluded from gold-filled endosomes while frequently being detected on ruthenium red-positive membranes. The composition of cellular marker proteins incorporated into HIV-1 supported a plasma membrane-derived origin of the viral envelope. Thus, contrary to current opinion, the plasma membrane is the primary site of HIV-1 budding also in infected macrophages.
url http://europepmc.org/articles/PMC1829407?pdf=render
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