Secretion of Hematopoietic Niche Signal Molecules under Conditions of Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells Induced by Relief Calcium Phosphate Coating

Bibliographic Details
Parent link:Biochemistry (Moscow), Supplement Series B: Biomedical Chemistry
Vol. 13, № 4.— 2019.— [P. 341-348]
Corporate Authors: Национальный исследовательский Томский политехнический университет Исследовательская школа физики высокоэнергетических процессов, Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
Other Authors: Litvinova L. S., Shupletsova V. V. Valeria, Yurova K. A., Khaziakhmatova O. G., Todosenko N. M. Natalia, Malashchenko V. V. Vladimir, Shunkin E. O. Egor, Melashchenko E. S., Khlusova M. Yu. Marina, Komarova E. G. Ekaterina, Chebodaeva V. V. Valentina Vadimovna, Sharkeev Yu. P. Yury Petrovich, Ivanov P. A. Pavel, Khlusov I. A. Igor Albertovich
Summary:Using a multiplex kit the secretion of a number of cytokines, chemokines, and growth factors has been investigated in vitro in a culture of human adipose-derived multipotent mesenchymal stromal cells (hAMMSCs) under conditions of their osteogenic differentiation caused by 14-day contact with a calcium phosphate (CP) surface of different roughness. Bilateral X-ray amorphous CP coatings were prepared on the samples of commercially pure titanium in the anodal regime using a microarc method. The electrolyte consisted of aqueous orthophosphoric acid (20 wt %), calcium carbonate (9 wt %), and synthetic hydroxyapatite nanopowder (6 wt %, particle diameter of 10-30 nm with single agglomerates up to 100 nm). hAMMSCs isolated from lipoaspirate were co-cultured after 4 passages with the CP-coated samples at a final concentration of 1.5•105 viable karyocytes per 1.5 mL of standard nutrition medium (without osteogenic stimulators) for 14 days (determination of the [CD45,34,14,20], CD73, CD90, and CD105 cell immunophenotype; analysis of secretory activity) and 21 days (alizarin red S cell culture staining) with medium replacement every 3-4 days. Under conditions of in vitro contact with rough CP coating hAMMSCs differentiated into osteoblasts synthesizing the mineralized bone matrix; this was accompanied by a 2−3-fold increase in the proportion of [CD45,34,14,20]+ hemopoietic cells. The following humoral factors of hemopoietic niches acted as the signal molecules escalating in vitro the hemopoietic base in 14 days of differentiating three-dimensional culture of hAMMSCs: leukemia inhibitory factor (LIF) and stem cell factor (SCF) cytokines in the case of the mean index of CP roughness Ra=2.4-2.6 µm or stromal derived factor-1 (SDF-1α, CXCL12 chemokine) in the case of Ra=3.1-4.4 µm.
Режим доступа: по договору с организацией-держателем ресурса
Language:English
Published: 2019
Subjects:
Online Access:https://doi.org/10.1134/S1990750819040048
Format: Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=663821

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200 1 |a Secretion of Hematopoietic Niche Signal Molecules under Conditions of Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells Induced by Relief Calcium Phosphate Coating  |f L. S. Litvinova, V. V. Shupletsova, K. A. Yurova [et al.] 
203 |a Text  |c electronic 
320 |a [References: 21 tit.] 
330 |a Using a multiplex kit the secretion of a number of cytokines, chemokines, and growth factors has been investigated in vitro in a culture of human adipose-derived multipotent mesenchymal stromal cells (hAMMSCs) under conditions of their osteogenic differentiation caused by 14-day contact with a calcium phosphate (CP) surface of different roughness. Bilateral X-ray amorphous CP coatings were prepared on the samples of commercially pure titanium in the anodal regime using a microarc method. The electrolyte consisted of aqueous orthophosphoric acid (20 wt %), calcium carbonate (9 wt %), and synthetic hydroxyapatite nanopowder (6 wt %, particle diameter of 10-30 nm with single agglomerates up to 100 nm). hAMMSCs isolated from lipoaspirate were co-cultured after 4 passages with the CP-coated samples at a final concentration of 1.5•105 viable karyocytes per 1.5 mL of standard nutrition medium (without osteogenic stimulators) for 14 days (determination of the [CD45,34,14,20], CD73, CD90, and CD105 cell immunophenotype; analysis of secretory activity) and 21 days (alizarin red S cell culture staining) with medium replacement every 3-4 days. Under conditions of in vitro contact with rough CP coating hAMMSCs differentiated into osteoblasts synthesizing the mineralized bone matrix; this was accompanied by a 2−3-fold increase in the proportion of [CD45,34,14,20]+ hemopoietic cells. The following humoral factors of hemopoietic niches acted as the signal molecules escalating in vitro the hemopoietic base in 14 days of differentiating three-dimensional culture of hAMMSCs: leukemia inhibitory factor (LIF) and stem cell factor (SCF) cytokines in the case of the mean index of CP roughness Ra=2.4-2.6 µm or stromal derived factor-1 (SDF-1α, CXCL12 chemokine) in the case of Ra=3.1-4.4 µm. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Biochemistry (Moscow), Supplement Series B: Biomedical Chemistry 
463 |t Vol. 13, № 4  |v [P. 341-348]  |d 2019 
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610 1 |a roughness index R a 
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701 1 |a Litvinova  |b L. S. 
701 1 |a Shupletsova  |b V. V.  |g Valeria 
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701 1 |a Todosenko  |b N. M.  |g Natalia 
701 1 |a Malashchenko  |b V. V.  |g Vladimir 
701 1 |a Shunkin  |b E. O.  |g Egor 
701 1 |a Melashchenko  |b E. S. 
701 1 |a Khlusova  |b M. Yu.  |g Marina 
701 1 |a Komarova  |b E. G.  |g Ekaterina 
701 1 |a Chebodaeva  |b V. V.  |c physicist  |c technician of Tomsk Polytechnic University  |f 1991-  |g Valentina Vadimovna  |3 (RuTPU)RU\TPU\pers\36333 
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 Ivanov  |b P. A.  |g Pavel 
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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