Evidence map›Paper›PMID 26834711›Full record

ArticleFrontiers in microbiology2015

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

Mai Izumida, Haruka Kamiyama, Takashi Suematsu, Eri Honda, Yosuke Koizumi, Kiyoshi Yasui, Hideki Hayashi, Koya Ariyoshi, Yoshinao Kubo

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Mai IzumidaDivision of Cytokine Signaling, Graduate School of Biomedical Sciences, Nagasaki UniversityNagasaki, Japan; Department of Clinical Medicine, Institute of Tropical Medicine, Nagasaki UniversityNagasaki, Japan.
Haruka KamiyamaDivision of Cytokine Signaling, Graduate School of Biomedical Sciences, Nagasaki UniversityNagasaki, Japan; Department of AIDS Research, Institute of Tropical Medicine, Nagasaki UniversityNagasaki, Japan.
Takashi SuematsuCentral Electron Microscope Laboratory, Nagasaki University School of Medicine Nagasaki, Japan.
Eri HondaDivision of Cytokine Signaling, Graduate School of Biomedical Sciences, Nagasaki University Nagasaki, Japan.
Yosuke KoizumiDivision of Cytokine Signaling, Graduate School of Biomedical Sciences, Nagasaki University Nagasaki, Japan.
Kiyoshi YasuiDivision of Cytokine Signaling, Graduate School of Biomedical Sciences, Nagasaki University Nagasaki, Japan.
Hideki HayashiDivision of Cytokine Signaling, Graduate School of Biomedical Sciences, Nagasaki University Nagasaki, Japan.
Koya AriyoshiDepartment of Clinical Medicine, Institute of Tropical Medicine, Nagasaki University Nagasaki, Japan.
Yoshinao KuboDivision of Cytokine Signaling, Graduate School of Biomedical Sciences, Nagasaki UniversityNagasaki, Japan; Department of AIDS Research, Institute of Tropical Medicine, Nagasaki UniversityNagasaki, Japan.
Nagasaki University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

cell-cell fusionendocytosisenvelopehuman immunodeficiency virusmurine leukemia virusretrovirus

Identifiers

PMID26834711
PMCPMC4717186
OpenAlexW2280221182

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.