Effect of virulent and vaccine variants of influenza virus on the immunophenotype of dendritic cells generated from murine bone marrow

The aim of this study was to generate dendritic cells from the bone marrow of mice (DC) in vitro and to assess the effect of virulent and attenuated variants of influenza virus on the maturation of DCs. Granulocyte-macrophage colony stimulating factor (GM-CSF) and interleukin-4 (IL-4) were used in c...

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Autores principales:	N. K. Akhmatova, A. A. Rtishchev, S. G. Markushin, A. M. Kostinova, E. A. Akhmatova, V. N. Stolpnikova, E. O. Kalinichenko, I. Zh. Shubina, I. A. Bisheva
Formato:	article
Lenguaje:	RU
Publicado:	SPb RAACI 2020
Materias:	cell culture dendritic cells morphology influenza virus virulent and attenuated variants differentiation markers toll-like receptors Immunologic diseases. Allergy RC581-607
Acceso en línea:	https://doaj.org/article/2bc3d3b1b4414b2eab7dd9123816182f
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spelling	oai:doaj.org-article:2bc3d3b1b4414b2eab7dd9123816182f2021-11-18T08:03:49ZEffect of virulent and vaccine variants of influenza virus on the immunophenotype of dendritic cells generated from murine bone marrow1563-06252313-741X10.15789/1563-0625-EOV-1869https://doaj.org/article/2bc3d3b1b4414b2eab7dd9123816182f2020-05-01T00:00:00Zhttps://www.mimmun.ru/mimmun/article/view/1869https://doaj.org/toc/1563-0625https://doaj.org/toc/2313-741XThe aim of this study was to generate dendritic cells from the bone marrow of mice (DC) in vitro and to assess the effect of virulent and attenuated variants of influenza virus on the maturation of DCs. Granulocyte-macrophage colony stimulating factor (GM-CSF) and interleukin-4 (IL-4) were used in combination, to induce differentiation of mouse bone marrow (BM) mononucleocytes into DCs. On the 5th day, distinct variants of influenza virus were added to the cell culture, and the cells were additionally incubated for 2 days. The morphological characteristics of DCs, immunophenotype of DCs and expression of some Toll-like receptors were evaluated. On the 5th day of incubation. the DCs acquired typical morphological characteristics. DCs were large in size with an eccentrically located nucleous, often irregular in shape, with numerous processes. On the 7th day of incubation with influenza virus variants, their cytoplasm was somewhat denser. DCs acquired more processes, necessary for intercellular contacts. Expression levels of CD11c, a specific marker of BM-derived DCs, and of co-stimulatory molecules such as CD40, CD80, CD86, and MHC-II were elevated in mature DCs. Virulent versus attenuated strains of the influenza virus induced special variants of DCs differentiation, with respect to expression rates of differentiation markers, as well as expression of Toll-like receptors and costimulatory molecules. Conclusions. The in vitro cultured murine mononucleocytes derived from bone marrow can produce a large number of n-DCs, that can mature in the presence of different variants.During evolution of the DC immunophenotype treated with variant influenza viruses, we have found distinct signs of immunosuppression.The attenuated U-2 and M-26 influenza variants obtained by site-specific mutagenesis upon development of DCs immunophenotype, exhibited a decreased immunosuppressive activity and were not inferior to the cold-adapted (CA) reassortant for the most positions, but exceeded it in some instances. These studies can help to assess the criteria for evaluation the efficiency of in vitro developed influenza vaccines.N. K. AkhmatovaA. A. RtishchevS. G. MarkushinA. M. KostinovaE. A. AkhmatovaV. N. StolpnikovaE. O. KalinichenkoI. Zh. ShubinaI. A. BishevaSPb RAACIarticlecell culturedendritic cellsmorphologyinfluenza virusvirulent and attenuated variantsdifferentiation markerstoll-like receptorsImmunologic diseases. AllergyRC581-607RUMedicinskaâ Immunologiâ, Vol 22, Iss 3, Pp 473-482 (2020)
institution	DOAJ
collection	DOAJ
language	RU
topic	cell culture dendritic cells morphology influenza virus virulent and attenuated variants differentiation markers toll-like receptors Immunologic diseases. Allergy RC581-607
spellingShingle	cell culture dendritic cells morphology influenza virus virulent and attenuated variants differentiation markers toll-like receptors Immunologic diseases. Allergy RC581-607 N. K. Akhmatova A. A. Rtishchev S. G. Markushin A. M. Kostinova E. A. Akhmatova V. N. Stolpnikova E. O. Kalinichenko I. Zh. Shubina I. A. Bisheva Effect of virulent and vaccine variants of influenza virus on the immunophenotype of dendritic cells generated from murine bone marrow
description	The aim of this study was to generate dendritic cells from the bone marrow of mice (DC) in vitro and to assess the effect of virulent and attenuated variants of influenza virus on the maturation of DCs. Granulocyte-macrophage colony stimulating factor (GM-CSF) and interleukin-4 (IL-4) were used in combination, to induce differentiation of mouse bone marrow (BM) mononucleocytes into DCs. On the 5th day, distinct variants of influenza virus were added to the cell culture, and the cells were additionally incubated for 2 days. The morphological characteristics of DCs, immunophenotype of DCs and expression of some Toll-like receptors were evaluated. On the 5th day of incubation. the DCs acquired typical morphological characteristics. DCs were large in size with an eccentrically located nucleous, often irregular in shape, with numerous processes. On the 7th day of incubation with influenza virus variants, their cytoplasm was somewhat denser. DCs acquired more processes, necessary for intercellular contacts. Expression levels of CD11c, a specific marker of BM-derived DCs, and of co-stimulatory molecules such as CD40, CD80, CD86, and MHC-II were elevated in mature DCs. Virulent versus attenuated strains of the influenza virus induced special variants of DCs differentiation, with respect to expression rates of differentiation markers, as well as expression of Toll-like receptors and costimulatory molecules. Conclusions. The in vitro cultured murine mononucleocytes derived from bone marrow can produce a large number of n-DCs, that can mature in the presence of different variants.During evolution of the DC immunophenotype treated with variant influenza viruses, we have found distinct signs of immunosuppression.The attenuated U-2 and M-26 influenza variants obtained by site-specific mutagenesis upon development of DCs immunophenotype, exhibited a decreased immunosuppressive activity and were not inferior to the cold-adapted (CA) reassortant for the most positions, but exceeded it in some instances. These studies can help to assess the criteria for evaluation the efficiency of in vitro developed influenza vaccines.
format	article
author	N. K. Akhmatova A. A. Rtishchev S. G. Markushin A. M. Kostinova E. A. Akhmatova V. N. Stolpnikova E. O. Kalinichenko I. Zh. Shubina I. A. Bisheva
author_facet	N. K. Akhmatova A. A. Rtishchev S. G. Markushin A. M. Kostinova E. A. Akhmatova V. N. Stolpnikova E. O. Kalinichenko I. Zh. Shubina I. A. Bisheva
author_sort	N. K. Akhmatova
title	Effect of virulent and vaccine variants of influenza virus on the immunophenotype of dendritic cells generated from murine bone marrow
title_short	Effect of virulent and vaccine variants of influenza virus on the immunophenotype of dendritic cells generated from murine bone marrow
title_full	Effect of virulent and vaccine variants of influenza virus on the immunophenotype of dendritic cells generated from murine bone marrow
title_fullStr	Effect of virulent and vaccine variants of influenza virus on the immunophenotype of dendritic cells generated from murine bone marrow
title_full_unstemmed	Effect of virulent and vaccine variants of influenza virus on the immunophenotype of dendritic cells generated from murine bone marrow
title_sort	effect of virulent and vaccine variants of influenza virus on the immunophenotype of dendritic cells generated from murine bone marrow
publisher	SPb RAACI
publishDate	2020
url	https://doaj.org/article/2bc3d3b1b4414b2eab7dd9123816182f
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Effect of virulent and vaccine variants of influenza virus on the immunophenotype of dendritic cells generated from murine bone marrow

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