Human Mesenchymal Stem Cells as a Carrier for a Cell-Mediated Drug Delivery; Frontiers in Bioengineering and Biotechnology; Vol. 10

Bibliografiset tiedot
Parent link:Frontiers in Bioengineering and Biotechnology
Vol. 10.— 2022.— [796111, 14 p.]
Yhteisötekijä: Национальный исследовательский Томский политехнический университет Инженерная школа природных ресурсов Отделение химической инженерии
Muut tekijät: Litvinova L. S., Shupletsova V. V. Valeria, Khaziakhmatova O. G., Daminova A. G., Kudryavtseva V. L., Yurova K. A., Malashchenko V. V., Todosenko N. M. Natalia, Popova V. A. Valentina Aleksandrovna, Litvinov R. I., Korotkova E. I. Elena Ivanovna, Sukhorukov G. B. Gleb, Gow A. J. Andrew, Weissman D., Atochina-Vasserman E. N., Khlusov I. A. Igor Albertovich
Yhteenveto:Title screen
A number of preclinical and clinical studies have demonstrated the efficiency of mesenchymal stromal cells to serve as an excellent base for a cell-mediated drug delivery system. Cell-based targeted drug delivery has received much attention as a system to facilitate the uptake a nd transfer of active substances to specific organs and tissues with high efficiency. Human mesenchymal stem cells (MSCs) are attracting increased interest as a promising tool for cell-based therapy due to their high proliferative capacity, multi-potency, and anti-inflammatory and immunomodulatory properties. In particular, these cells are potentially suitable for use as encapsulated drug transporters to sites of inflammation. Here, we studied the in vitro effects of incorporating synthetic polymer microcapsules at various microcapsule-to-cell ratios on the morphology, ultrastructure, cytokine profile, and migration ability of human adipose-derived MSCs at various time points post-phagocytosis. The data show that under appropriate conditions, human MSCs can be efficiently loaded with synthesized microcapsules without damaging the cell’s structural integrity with unexpressed cytokine secretion, retained motility, and ability to migrate through 8 ?m pores. Thus, the strategy of using human MSCs as a delivery vehicle for transferring microcapsules, containing bioactive material, across the tissue–blood or tumor–blood barriers to facilitate the treatment of stroke, cancer, or inflammatory diseases may open a new therapeutic perspective.
Kieli:englanti
Julkaistu: 2022
Aiheet:
Linkit:http://earchive.tpu.ru/handle/11683/70707
https://doi.org/10.3389/fbioe.2022.796111
Aineistotyyppi: Elektroninen Kirjan osa
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=667536

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200 1 |a Human Mesenchymal Stem Cells as a Carrier for a Cell-Mediated Drug Delivery  |f L. S. Litvinova, V. V. Shupletsova, O. G. Khaziakhmatova [et al.] 
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300 |a Title screen 
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330 |a A number of preclinical and clinical studies have demonstrated the efficiency of mesenchymal stromal cells to serve as an excellent base for a cell-mediated drug delivery system. Cell-based targeted drug delivery has received much attention as a system to facilitate the uptake a nd transfer of active substances to specific organs and tissues with high efficiency. Human mesenchymal stem cells (MSCs) are attracting increased interest as a promising tool for cell-based therapy due to their high proliferative capacity, multi-potency, and anti-inflammatory and immunomodulatory properties. In particular, these cells are potentially suitable for use as encapsulated drug transporters to sites of inflammation. Here, we studied the in vitro effects of incorporating synthetic polymer microcapsules at various microcapsule-to-cell ratios on the morphology, ultrastructure, cytokine profile, and migration ability of human adipose-derived MSCs at various time points post-phagocytosis. The data show that under appropriate conditions, human MSCs can be efficiently loaded with synthesized microcapsules without damaging the cell’s structural integrity with unexpressed cytokine secretion, retained motility, and ability to migrate through 8 ?m pores. Thus, the strategy of using human MSCs as a delivery vehicle for transferring microcapsules, containing bioactive material, across the tissue–blood or tumor–blood barriers to facilitate the treatment of stroke, cancer, or inflammatory diseases may open a new therapeutic perspective. 
461 |t Frontiers in Bioengineering and Biotechnology 
463 |t Vol. 10  |v [796111, 14 p.]  |d 2022 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a human adipose-derived mesenchymal stromal/stem cells 
610 1 |a cell migration 
610 1 |a target drug delivery 
610 1 |a cellmediated drug delivery 
610 1 |a synthetic microcapsules 
610 1 |a стволовые клетки 
610 1 |a жировые ткани 
610 1 |a клеточная миграция 
610 1 |a адресная доставка 
610 1 |a микрокапсулы 
610 1 |a лекарства 
701 1 |a Litvinova  |b L. S. 
701 1 |a Shupletsova  |b V. V.  |g Valeria 
701 1 |a Khaziakhmatova  |b O. G. 
701 1 |a Daminova  |b A. G. 
701 1 |a Kudryavtseva  |b V. L. 
701 1 |a Yurova  |b K. A. 
701 1 |a Malashchenko  |b V. V. 
701 1 |a Todosenko  |b N. M.  |g Natalia 
701 1 |a Popova  |b V. A.  |c chemist  |c engineer of Tomsk Polytechnic University  |f 1993-  |g Valentina Aleksandrovna  |3 (RuTPU)RU\TPU\pers\46100 
701 1 |a Litvinov  |b R. I. 
701 1 |a Korotkova  |b E. I.  |c chemist  |c Professor of Tomsk Polytechnic University, Doctor of chemical science  |f 1965-  |g Elena Ivanovna  |3 (RuTPU)RU\TPU\pers\31278  |9 15456 
701 1 |a Sukhorukov  |b G. B.  |g Gleb 
701 1 |a Gow  |b A. J.  |g Andrew 
701 1 |a Weissman  |b D. 
701 1 |a Atochina-Vasserman  |b E. N. 
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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