The Morphofunctional Response of T-Lymphocytes to in vitro Contact with a Calcium Phosphate Coating in the Presence of a T-Cell Activator; Cell and Tissue Biology; Vol. 15, iss. 1

Dades bibliogràfiques
Parent link:Cell and Tissue Biology
Vol. 15, iss. 1.— 2021.— [P. 51–60]
Autor corporatiu: Национальный исследовательский Томский политехнический университет Исследовательская школа физики высокоэнергетических процессов, Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
Altres autors: Litvinova L. S. Larisa Sergeevna, Melashchenko E. S. Elena Sergeevna, Khaziakhmatova O. G. Olga Gennadjevna, Yurova K. A. Kristina Alekseevna, Sharkeev Yu. P. Yury Petrovich, Komarova E. G. Ekaterina Gennadjevna, Sedelnikova M. B. Mariya Borisovna, Todosenko N. M. Nataljya Mikhaylovna, Khlusov I. A. Igor Albertovich
Sumari:Title screen
The paper reports a study of the morphofunctional activity of T-lymphocytes in response to the in vitro contact with calcium phosphate (CP) coating in the presence of the particles bearing antibodies against CD2, CD3, and CD28 antigens. VT1-0 titanium plates (10 × 10 × 1 mm3 ) with a double-sided microarc rough (Ra=2-5 μm) CP coating were used as the model samples of the mineral matrix of the bone tissue. Magnetic particles (MACSiBeadTM T-cell Activation/Expansion Kit human) bearing antibodies to CD2, CD3, and CD28 antigens were used as a T-cell activator (TCA) simulating the signals produced by antigenpresenting cells (APCs). Mononuclear cells (MNCs) isolated from human blood (98.8% of CD45CD3+ cells) were cultured in the presence of samples with a CP coating and/or TCA (2 × 106 particles in 1.5 mL of nutritive medium in the proportion of 2 : 1 to cells) for 2 and 14 days. The CP coating and TCA triggered MNC culture adaptation in a synergic way via the mechanisms of hyperactivation and subsequent death of T-lymphocytes.
Immune selection occurred through the accumulation of the naive CD45RA+/RO+ T-lymphocytes and memory T-cells with the simultaneous depletion of the CD4+ and CD8+ T-cell pool. The shift in the T-lymphocyte populations was observed together with the increase (after 48 h of culturing) in the cell secretion activity with its subsequent decrease by the 14th day of observation. CP coating sustained (compared with the cell culture grown on plastic) the secretion ability of Th1 (IL-12, TNFα, and IFNγ) and Th2 (IL-4, IL-6, IL-10, and IL-13) lymphocytes. At the same time, the prolonged TCA signal after the 48-h activation caused the depletion of T-cell secretion. The suggestion that the observed in vitro effects may play role in the switching of signaling between T-lymphocytes, APCs, and CP materials at the cell-foreign body interface, which may result in a change in the inflammation phase, development of immune tolerance, successful osseointegration of the implant, or bone tissue remodeling impairment, is discussed.
Режим доступа: по договору с организацией-держателем ресурса
Idioma:anglès
Publicat: 2021
Matèries:
Accés en línia:https://doi.org/10.1134/S1990519X21010077
Format: Electrònic Capítol de llibre
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=667628

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200 1 |a The Morphofunctional Response of T-Lymphocytes to in vitro Contact with a Calcium Phosphate Coating in the Presence of a T-Cell Activator  |f L. S. Litvinova, E. S. Melashchenko, O. G. Khaziakhmatova [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 40 tit.] 
330 |a The paper reports a study of the morphofunctional activity of T-lymphocytes in response to the in vitro contact with calcium phosphate (CP) coating in the presence of the particles bearing antibodies against CD2, CD3, and CD28 antigens. VT1-0 titanium plates (10 × 10 × 1 mm3 ) with a double-sided microarc rough (Ra=2-5 μm) CP coating were used as the model samples of the mineral matrix of the bone tissue. Magnetic particles (MACSiBeadTM T-cell Activation/Expansion Kit human) bearing antibodies to CD2, CD3, and CD28 antigens were used as a T-cell activator (TCA) simulating the signals produced by antigenpresenting cells (APCs). Mononuclear cells (MNCs) isolated from human blood (98.8% of CD45CD3+ cells) were cultured in the presence of samples with a CP coating and/or TCA (2 × 106 particles in 1.5 mL of nutritive medium in the proportion of 2 : 1 to cells) for 2 and 14 days. The CP coating and TCA triggered MNC culture adaptation in a synergic way via the mechanisms of hyperactivation and subsequent death of T-lymphocytes. 
330 |a Immune selection occurred through the accumulation of the naive CD45RA+/RO+ T-lymphocytes and memory T-cells with the simultaneous depletion of the CD4+ and CD8+ T-cell pool. The shift in the T-lymphocyte populations was observed together with the increase (after 48 h of culturing) in the cell secretion activity with its subsequent decrease by the 14th day of observation. CP coating sustained (compared with the cell culture grown on plastic) the secretion ability of Th1 (IL-12, TNFα, and IFNγ) and Th2 (IL-4, IL-6, IL-10, and IL-13) lymphocytes. At the same time, the prolonged TCA signal after the 48-h activation caused the depletion of T-cell secretion. The suggestion that the observed in vitro effects may play role in the switching of signaling between T-lymphocytes, APCs, and CP materials at the cell-foreign body interface, which may result in a change in the inflammation phase, development of immune tolerance, successful osseointegration of the implant, or bone tissue remodeling impairment, is discussed. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
338 |b Российский научный фонд  |d 16-15-10031 
461 |t Cell and Tissue Biology 
463 |t Vol. 15, iss. 1  |v [P. 51–60]  |d 2021 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a human blood mononuclear leukocytes 
610 1 |a short- and long-term cultures 
610 1 |a viability 
610 1 |a immune phenotype 
610 1 |a cytokines 
610 1 |a anti-CD2CD3СD28 particles 
610 1 |a microarc calcium phosphate coating 
610 1 |a лейкоциты 
610 1 |a кровь 
610 1 |a жизнеспособность 
610 1 |a цитокины 
610 1 |a кальций-фосфатные покрытия 
701 1 |a Litvinova  |b L. S.  |g Larisa Sergeevna 
701 1 |a Melashchenko  |b E. S.  |g Elena Sergeevna 
701 1 |a Khaziakhmatova  |b O. G.  |g Olga Gennadjevna 
701 1 |a Yurova  |b K. A.  |g Kristina Alekseevna 
701 1 |a Sharkeev  |b Yu. P.  |c physicist  |c Professor of Tomsk Polytechnic University, Doctor of physical and mathematical sciences  |f 1950-  |g Yury Petrovich  |3 (RuTPU)RU\TPU\pers\32228  |9 16228 
701 1 |a Komarova  |b E. G.  |g Ekaterina Gennadjevna 
701 1 |a Sedelnikova  |b M. B.  |g Mariya Borisovna 
701 1 |a Todosenko  |b N. M.  |g Nataljya Mikhaylovna 
701 1 |a Khlusov  |b I. A.  |c biophysicist  |c Professor of Tomsk Polytechnic University, doctor of medical Sciences  |f 1963-  |g Igor Albertovich  |3 (RuTPU)RU\TPU\pers\34907  |9 18225 
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712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Исследовательская школа химических и биомедицинских технологий  |c (2017- )  |3 (RuTPU)RU\TPU\col\23537 
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