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Fragments of Target Cells are Internalized into Retroviral Envelope Protein-Expressing Cells during Cell-Cell Fusion by Endocytosis

Retroviruses enter into host cells by fusion between viral and host cell membranes. Retroviral envelope glycoprotein (Env) induces the membrane fusion, and also mediates cell-cell fusion. There are two types of cell-cell fusions induced by the Env protein. Fusion-from-within is induced by fusion bet...

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Autores principales: Izumida, Mai, Kamiyama, Haruka, Suematsu, Takashi, Honda, Eri, Koizumi, Yosuke, Yasui, Kiyoshi, Hayashi, Hideki, Ariyoshi, Koya, Kubo, Yoshinao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717186/
https://www.ncbi.nlm.nih.gov/pubmed/26834711
http://dx.doi.org/10.3389/fmicb.2015.01552
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author Izumida, Mai
Kamiyama, Haruka
Suematsu, Takashi
Honda, Eri
Koizumi, Yosuke
Yasui, Kiyoshi
Hayashi, Hideki
Ariyoshi, Koya
Kubo, Yoshinao
author_facet Izumida, Mai
Kamiyama, Haruka
Suematsu, Takashi
Honda, Eri
Koizumi, Yosuke
Yasui, Kiyoshi
Hayashi, Hideki
Ariyoshi, Koya
Kubo, Yoshinao
author_sort Izumida, Mai
collection PubMed
description Retroviruses enter into host cells by fusion between viral and host cell membranes. Retroviral envelope glycoprotein (Env) induces the membrane fusion, and also mediates cell-cell fusion. There are two types of cell-cell fusions induced by the Env protein. Fusion-from-within is induced by fusion between viral fusogenic Env protein-expressing cells and susceptible cells, and virions induce fusion-from-without by fusion between adjacent cells. Although entry of ecotropic murine leukemia virus (E-MLV) requires host cell endocytosis, the involvement of endocytosis in cell fusion is unclear. By fluorescent microscopic analysis of the fusion-from-within, we found that fragments of target cells are internalized into Env-expressing cells. Treatment of the Env-expressing cells with an endocytosis inhibitor more significantly inhibited the cell fusion than that of the target cells, indicating that endocytosis in Env-expressing cells is required for the cell fusion. The endocytosis inhibitor also attenuated the fusion-from-without. Electron microscopic analysis suggested that the membrane fusion resulting in fusion-from-within initiates in endocytic membrane dents. This study shows that two types of the viral cell fusion both require endocytosis, and provides the cascade of fusion-from-within.
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spelling pubmed-47171862016-01-29 Fragments of Target Cells are Internalized into Retroviral Envelope Protein-Expressing Cells during Cell-Cell Fusion by Endocytosis Izumida, Mai Kamiyama, Haruka Suematsu, Takashi Honda, Eri Koizumi, Yosuke Yasui, Kiyoshi Hayashi, Hideki Ariyoshi, Koya Kubo, Yoshinao Front Microbiol Microbiology Retroviruses enter into host cells by fusion between viral and host cell membranes. Retroviral envelope glycoprotein (Env) induces the membrane fusion, and also mediates cell-cell fusion. There are two types of cell-cell fusions induced by the Env protein. Fusion-from-within is induced by fusion between viral fusogenic Env protein-expressing cells and susceptible cells, and virions induce fusion-from-without by fusion between adjacent cells. Although entry of ecotropic murine leukemia virus (E-MLV) requires host cell endocytosis, the involvement of endocytosis in cell fusion is unclear. By fluorescent microscopic analysis of the fusion-from-within, we found that fragments of target cells are internalized into Env-expressing cells. Treatment of the Env-expressing cells with an endocytosis inhibitor more significantly inhibited the cell fusion than that of the target cells, indicating that endocytosis in Env-expressing cells is required for the cell fusion. The endocytosis inhibitor also attenuated the fusion-from-without. Electron microscopic analysis suggested that the membrane fusion resulting in fusion-from-within initiates in endocytic membrane dents. This study shows that two types of the viral cell fusion both require endocytosis, and provides the cascade of fusion-from-within. Frontiers Media S.A. 2016-01-19 /pmc/articles/PMC4717186/ /pubmed/26834711 http://dx.doi.org/10.3389/fmicb.2015.01552 Text en Copyright © 2016 Izumida, Kamiyama, Suematsu, Honda, Koizumi, Yasui, Hayashi, Ariyoshi and Kubo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Izumida, Mai
Kamiyama, Haruka
Suematsu, Takashi
Honda, Eri
Koizumi, Yosuke
Yasui, Kiyoshi
Hayashi, Hideki
Ariyoshi, Koya
Kubo, Yoshinao
Fragments of Target Cells are Internalized into Retroviral Envelope Protein-Expressing Cells during Cell-Cell Fusion by Endocytosis
title Fragments of Target Cells are Internalized into Retroviral Envelope Protein-Expressing Cells during Cell-Cell Fusion by Endocytosis
title_full Fragments of Target Cells are Internalized into Retroviral Envelope Protein-Expressing Cells during Cell-Cell Fusion by Endocytosis
title_fullStr Fragments of Target Cells are Internalized into Retroviral Envelope Protein-Expressing Cells during Cell-Cell Fusion by Endocytosis
title_full_unstemmed Fragments of Target Cells are Internalized into Retroviral Envelope Protein-Expressing Cells during Cell-Cell Fusion by Endocytosis
title_short Fragments of Target Cells are Internalized into Retroviral Envelope Protein-Expressing Cells during Cell-Cell Fusion by Endocytosis
title_sort fragments of target cells are internalized into retroviral envelope protein-expressing cells during cell-cell fusion by endocytosis
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717186/
https://www.ncbi.nlm.nih.gov/pubmed/26834711
http://dx.doi.org/10.3389/fmicb.2015.01552
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