A Comprehensive Analysis of Human Endogenous Retroviruses HERV-K (HML.2) from Teratocarcinoma Cell Lines and Detection of Viral Cargo in Microvesicles

About 8% of our genome is composed of sequences from Human Endogenous Retroviruses (HERVs). The HERV-K (HML.2) family, here abbreviated HML.2, is able to produce virus particles that were detected in cell lines, malignant tumors and in autoimmune diseases. Parameters and properties of HML.2 released...

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Autores principales: Vladimir A. Morozov, Alexey V. Morozov
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:cb2f380eb61c4257bcb168b58714d47b2021-11-25T17:56:17ZA Comprehensive Analysis of Human Endogenous Retroviruses HERV-K (HML.2) from Teratocarcinoma Cell Lines and Detection of Viral Cargo in Microvesicles10.3390/ijms2222123981422-00671661-6596https://doaj.org/article/cb2f380eb61c4257bcb168b58714d47b2021-11-01T00:00:00Zhttps://www.mdpi.com/1422-0067/22/22/12398https://doaj.org/toc/1661-6596https://doaj.org/toc/1422-0067About 8% of our genome is composed of sequences from Human Endogenous Retroviruses (HERVs). The HERV-K (HML.2) family, here abbreviated HML.2, is able to produce virus particles that were detected in cell lines, malignant tumors and in autoimmune diseases. Parameters and properties of HML.2 released from teratocarcinoma cell lines GH and Tera-1 were investigated in detail. In most experiments, analyzed viruses were purified by density gradient centrifugation. HML.2 structural proteins, reverse transcriptase (RT) activity, viral RNA (vRNA) and particle morphology were analyzed. The HML.2 markers were predominantly detected in fractions with a buoyant density of 1.16 g/cm<sup>3</sup>. Deglycosylation of TM revealed truncated forms of transmembrane (TM) protein. Free virions and extracellular vesicles (presumably microvesicles—MVs) with HML.2 elements, including budding intermediates, were detected by electron microscopy. Viral elements and assembled virions captured and exported by MVs can boost specific immune responses and trigger immunomodulation in recipient cells. Sequencing of cDNA clones demonstrated exclusive presence of HERV-K108 <i>env</i> in HML.2 from Tera-1 cells. Not counting two recombinant variants, four known <i>env</i> sequences were found in HML.2 from GH cells. Obtained results shed light on parameters and morphology of HML.2. A possible mechanism of HML.2-induced diseases is discussed.Vladimir A. MorozovAlexey V. MorozovMDPI AGarticleteratocarcinomahuman endogenous retrovirusesproteinsdeglycosylationelectron microscopyviral RNABiology (General)QH301-705.5ChemistryQD1-999ENInternational Journal of Molecular Sciences, Vol 22, Iss 12398, p 12398 (2021)
institution DOAJ
collection DOAJ
language EN
topic teratocarcinoma
human endogenous retroviruses
proteins
deglycosylation
electron microscopy
viral RNA
Biology (General)
QH301-705.5
Chemistry
QD1-999
spellingShingle teratocarcinoma
human endogenous retroviruses
proteins
deglycosylation
electron microscopy
viral RNA
Biology (General)
QH301-705.5
Chemistry
QD1-999
Vladimir A. Morozov
Alexey V. Morozov
A Comprehensive Analysis of Human Endogenous Retroviruses HERV-K (HML.2) from Teratocarcinoma Cell Lines and Detection of Viral Cargo in Microvesicles
description About 8% of our genome is composed of sequences from Human Endogenous Retroviruses (HERVs). The HERV-K (HML.2) family, here abbreviated HML.2, is able to produce virus particles that were detected in cell lines, malignant tumors and in autoimmune diseases. Parameters and properties of HML.2 released from teratocarcinoma cell lines GH and Tera-1 were investigated in detail. In most experiments, analyzed viruses were purified by density gradient centrifugation. HML.2 structural proteins, reverse transcriptase (RT) activity, viral RNA (vRNA) and particle morphology were analyzed. The HML.2 markers were predominantly detected in fractions with a buoyant density of 1.16 g/cm<sup>3</sup>. Deglycosylation of TM revealed truncated forms of transmembrane (TM) protein. Free virions and extracellular vesicles (presumably microvesicles—MVs) with HML.2 elements, including budding intermediates, were detected by electron microscopy. Viral elements and assembled virions captured and exported by MVs can boost specific immune responses and trigger immunomodulation in recipient cells. Sequencing of cDNA clones demonstrated exclusive presence of HERV-K108 <i>env</i> in HML.2 from Tera-1 cells. Not counting two recombinant variants, four known <i>env</i> sequences were found in HML.2 from GH cells. Obtained results shed light on parameters and morphology of HML.2. A possible mechanism of HML.2-induced diseases is discussed.
format article
author Vladimir A. Morozov
Alexey V. Morozov
author_facet Vladimir A. Morozov
Alexey V. Morozov
author_sort Vladimir A. Morozov
title A Comprehensive Analysis of Human Endogenous Retroviruses HERV-K (HML.2) from Teratocarcinoma Cell Lines and Detection of Viral Cargo in Microvesicles
title_short A Comprehensive Analysis of Human Endogenous Retroviruses HERV-K (HML.2) from Teratocarcinoma Cell Lines and Detection of Viral Cargo in Microvesicles
title_full A Comprehensive Analysis of Human Endogenous Retroviruses HERV-K (HML.2) from Teratocarcinoma Cell Lines and Detection of Viral Cargo in Microvesicles
title_fullStr A Comprehensive Analysis of Human Endogenous Retroviruses HERV-K (HML.2) from Teratocarcinoma Cell Lines and Detection of Viral Cargo in Microvesicles
title_full_unstemmed A Comprehensive Analysis of Human Endogenous Retroviruses HERV-K (HML.2) from Teratocarcinoma Cell Lines and Detection of Viral Cargo in Microvesicles
title_sort comprehensive analysis of human endogenous retroviruses herv-k (hml.2) from teratocarcinoma cell lines and detection of viral cargo in microvesicles
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/cb2f380eb61c4257bcb168b58714d47b
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