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Mechanisms of virus dissemination in bone marrow of HIV-1–infected humanized BLT mice

Immune progenitor cells differentiate in bone marrow (BM) and then migrate to tissues. HIV-1 infects multiple BM cell types, but virus dissemination within BM has been poorly understood. We used light microscopy and electron tomography to elucidate mechanisms of HIV-1 dissemination within BM of HIV-...

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Autores principales: Ladinsky, Mark S, Khamaikawin, Wannisa, Jung, Yujin, Lin, Samantha, Lam, Jennifer, An, Dong Sung, Bjorkman, Pamela J, Kieffer, Collin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839903/
https://www.ncbi.nlm.nih.gov/pubmed/31657719
http://dx.doi.org/10.7554/eLife.46916
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author Ladinsky, Mark S
Khamaikawin, Wannisa
Jung, Yujin
Lin, Samantha
Lam, Jennifer
An, Dong Sung
Bjorkman, Pamela J
Kieffer, Collin
author_facet Ladinsky, Mark S
Khamaikawin, Wannisa
Jung, Yujin
Lin, Samantha
Lam, Jennifer
An, Dong Sung
Bjorkman, Pamela J
Kieffer, Collin
author_sort Ladinsky, Mark S
collection PubMed
description Immune progenitor cells differentiate in bone marrow (BM) and then migrate to tissues. HIV-1 infects multiple BM cell types, but virus dissemination within BM has been poorly understood. We used light microscopy and electron tomography to elucidate mechanisms of HIV-1 dissemination within BM of HIV-1–infected BM/liver/thymus (BLT) mice. Tissue clearing combined with confocal and light sheet fluorescence microscopy revealed distinct populations of HIV-1 p24-producing cells in BM early after infection, and quantification of these populations identified macrophages as the principal subset of virus-producing cells in BM over time. Electron tomography demonstrated three modes of HIV-1 dissemination in BM: (i) semi-synchronous budding from T-cell and macrophage membranes, (ii) mature virus association with virus-producing T-cell uropods contacting putative target cells, and (iii) macrophages engulfing HIV-1–producing T-cells and producing virus within enclosed intracellular compartments that fused to invaginations with access to the extracellular space. These results illustrate mechanisms by which the specialized environment of the BM can promote virus spread locally and to distant lymphoid tissues.
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spelling pubmed-68399032019-11-12 Mechanisms of virus dissemination in bone marrow of HIV-1–infected humanized BLT mice Ladinsky, Mark S Khamaikawin, Wannisa Jung, Yujin Lin, Samantha Lam, Jennifer An, Dong Sung Bjorkman, Pamela J Kieffer, Collin eLife Human Biology and Medicine Immune progenitor cells differentiate in bone marrow (BM) and then migrate to tissues. HIV-1 infects multiple BM cell types, but virus dissemination within BM has been poorly understood. We used light microscopy and electron tomography to elucidate mechanisms of HIV-1 dissemination within BM of HIV-1–infected BM/liver/thymus (BLT) mice. Tissue clearing combined with confocal and light sheet fluorescence microscopy revealed distinct populations of HIV-1 p24-producing cells in BM early after infection, and quantification of these populations identified macrophages as the principal subset of virus-producing cells in BM over time. Electron tomography demonstrated three modes of HIV-1 dissemination in BM: (i) semi-synchronous budding from T-cell and macrophage membranes, (ii) mature virus association with virus-producing T-cell uropods contacting putative target cells, and (iii) macrophages engulfing HIV-1–producing T-cells and producing virus within enclosed intracellular compartments that fused to invaginations with access to the extracellular space. These results illustrate mechanisms by which the specialized environment of the BM can promote virus spread locally and to distant lymphoid tissues. eLife Sciences Publications, Ltd 2019-10-28 /pmc/articles/PMC6839903/ /pubmed/31657719 http://dx.doi.org/10.7554/eLife.46916 Text en © 2019, Ladinsky et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Human Biology and Medicine
Ladinsky, Mark S
Khamaikawin, Wannisa
Jung, Yujin
Lin, Samantha
Lam, Jennifer
An, Dong Sung
Bjorkman, Pamela J
Kieffer, Collin
Mechanisms of virus dissemination in bone marrow of HIV-1–infected humanized BLT mice
title Mechanisms of virus dissemination in bone marrow of HIV-1–infected humanized BLT mice
title_full Mechanisms of virus dissemination in bone marrow of HIV-1–infected humanized BLT mice
title_fullStr Mechanisms of virus dissemination in bone marrow of HIV-1–infected humanized BLT mice
title_full_unstemmed Mechanisms of virus dissemination in bone marrow of HIV-1–infected humanized BLT mice
title_short Mechanisms of virus dissemination in bone marrow of HIV-1–infected humanized BLT mice
title_sort mechanisms of virus dissemination in bone marrow of hiv-1–infected humanized blt mice
topic Human Biology and Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839903/
https://www.ncbi.nlm.nih.gov/pubmed/31657719
http://dx.doi.org/10.7554/eLife.46916
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