EVALUATION OF MICROVESICLES FORMED BY NATURAL KILLER (NK) CELLS USING FLOW CYTOMETRY

As a result of activation and/or apoptosis, the cells can form microvesicles (MV) from 100 nm up to 1000 nm in size. Nowadays, the attention is being increasingly focused on dynamic detection and evaluation of leukocyte-derived microvesicles by their contents. In this regard, determination of microv...

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Autores principales: V. A. Mikhailova, K. L. Belyakova, L. P. Vyazmina, A. R. Sheveleva, S. A. Selkov, D. I. Sokolov
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Lenguaje:RU
Publicado: SPb RAACI 2018
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Acceso en línea:https://doaj.org/article/60a9edc57c0642f099f7cd2875c27de7
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spelling oai:doaj.org-article:60a9edc57c0642f099f7cd2875c27de72021-11-18T08:03:47ZEVALUATION OF MICROVESICLES FORMED BY NATURAL KILLER (NK) CELLS USING FLOW CYTOMETRY1563-06252313-741X10.15789/1563-0625-2018-2-251-254https://doaj.org/article/60a9edc57c0642f099f7cd2875c27de72018-03-01T00:00:00Zhttps://www.mimmun.ru/mimmun/article/view/1482https://doaj.org/toc/1563-0625https://doaj.org/toc/2313-741XAs a result of activation and/or apoptosis, the cells can form microvesicles (MV) from 100 nm up to 1000 nm in size. Nowadays, the attention is being increasingly focused on dynamic detection and evaluation of leukocyte-derived microvesicles by their contents. In this regard, determination of microvesicles formed by NK cells is of utmost interest. The main function of these population is to induce apoptosis of virus-infected and tumor cells. At the present time, there is no direct evidence of the NK cells ability to produce microvesicles. This investigation was performed in order to estimate contents of NK cell-derived microvesicles using highprecision flow cytometric approach. It has been shown that the high-precision flow cytometry allows to detect microvesicles formed by NK cells, ranging from 200 to 1000 nm in size. It was demonstrated that incubation of NK cells in the presence of TNFα did not affect the relative value of microvesicles, however, being associated with increased intensity of CD95 expression on microvesicles. Hence, the high-precision flow cytometry can be used to detect microvesicles and to determine their phenotype.V. A. MikhailovaK. L. BelyakovaL. P. VyazminaA. R. ShevelevaS. A. SelkovD. I. SokolovSPb RAACIarticlenk cellsflow cytometrymicrovesiclesmicroparticlescell culturenk-92cell surface receptorsImmunologic diseases. AllergyRC581-607RUMedicinskaâ Immunologiâ, Vol 20, Iss 2, Pp 251-254 (2018)
institution DOAJ
collection DOAJ
language RU
topic nk cells
flow cytometry
microvesicles
microparticles
cell culture
nk-92
cell surface receptors
Immunologic diseases. Allergy
RC581-607
spellingShingle nk cells
flow cytometry
microvesicles
microparticles
cell culture
nk-92
cell surface receptors
Immunologic diseases. Allergy
RC581-607
V. A. Mikhailova
K. L. Belyakova
L. P. Vyazmina
A. R. Sheveleva
S. A. Selkov
D. I. Sokolov
EVALUATION OF MICROVESICLES FORMED BY NATURAL KILLER (NK) CELLS USING FLOW CYTOMETRY
description As a result of activation and/or apoptosis, the cells can form microvesicles (MV) from 100 nm up to 1000 nm in size. Nowadays, the attention is being increasingly focused on dynamic detection and evaluation of leukocyte-derived microvesicles by their contents. In this regard, determination of microvesicles formed by NK cells is of utmost interest. The main function of these population is to induce apoptosis of virus-infected and tumor cells. At the present time, there is no direct evidence of the NK cells ability to produce microvesicles. This investigation was performed in order to estimate contents of NK cell-derived microvesicles using highprecision flow cytometric approach. It has been shown that the high-precision flow cytometry allows to detect microvesicles formed by NK cells, ranging from 200 to 1000 nm in size. It was demonstrated that incubation of NK cells in the presence of TNFα did not affect the relative value of microvesicles, however, being associated with increased intensity of CD95 expression on microvesicles. Hence, the high-precision flow cytometry can be used to detect microvesicles and to determine their phenotype.
format article
author V. A. Mikhailova
K. L. Belyakova
L. P. Vyazmina
A. R. Sheveleva
S. A. Selkov
D. I. Sokolov
author_facet V. A. Mikhailova
K. L. Belyakova
L. P. Vyazmina
A. R. Sheveleva
S. A. Selkov
D. I. Sokolov
author_sort V. A. Mikhailova
title EVALUATION OF MICROVESICLES FORMED BY NATURAL KILLER (NK) CELLS USING FLOW CYTOMETRY
title_short EVALUATION OF MICROVESICLES FORMED BY NATURAL KILLER (NK) CELLS USING FLOW CYTOMETRY
title_full EVALUATION OF MICROVESICLES FORMED BY NATURAL KILLER (NK) CELLS USING FLOW CYTOMETRY
title_fullStr EVALUATION OF MICROVESICLES FORMED BY NATURAL KILLER (NK) CELLS USING FLOW CYTOMETRY
title_full_unstemmed EVALUATION OF MICROVESICLES FORMED BY NATURAL KILLER (NK) CELLS USING FLOW CYTOMETRY
title_sort evaluation of microvesicles formed by natural killer (nk) cells using flow cytometry
publisher SPb RAACI
publishDate 2018
url https://doaj.org/article/60a9edc57c0642f099f7cd2875c27de7
work_keys_str_mv AT vamikhailova evaluationofmicrovesiclesformedbynaturalkillernkcellsusingflowcytometry
AT klbelyakova evaluationofmicrovesiclesformedbynaturalkillernkcellsusingflowcytometry
AT lpvyazmina evaluationofmicrovesiclesformedbynaturalkillernkcellsusingflowcytometry
AT arsheveleva evaluationofmicrovesiclesformedbynaturalkillernkcellsusingflowcytometry
AT saselkov evaluationofmicrovesiclesformedbynaturalkillernkcellsusingflowcytometry
AT disokolov evaluationofmicrovesiclesformedbynaturalkillernkcellsusingflowcytometry
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