TY - JOUR
T1 - Human Mesenchymal Stem Cells as a Carrier for a Cell-Mediated Drug Delivery
AU - Litvinova, L. S.
AU - Shupletsova, V. V.
AU - Khaziakhmatova, O. G.
AU - Daminova, A. G.
AU - Kudryavtseva, V. L.
AU - Yurova, K. A.
AU - Malashchenko, V. V.
AU - Todosenko, N. M.
AU - Popova, V.
AU - Litvinov, R. I.
AU - Korotkova, E. I.
AU - Sukhorukov, G. B.
AU - Gow, A. J.
AU - Weissman, D.
AU - Atochina-Vasserman, E. N.
AU - Khlusov, I. A.
N1 - Funding Information:
The authors are grateful to the financial support provided by the State support of Leading Scientific Schools of the Russian Federation, No. 2495.2020.7 (LSL), and the Strategic Academic Leadership Program PRIORITY 2030 at Kazan Federal University (RIL and AGD) and Siberian State Medical University (IAK).
Publisher Copyright:
Copyright © 2022 Litvinova, Shupletsova, Khaziakhmatova, Daminova, Kudryavtseva, Yurova, Malashchenko, Todosenko, Popova, Litvinov, Korotkova, Sukhorukov, Gow, Weissman, Atochina-Vasserman and Khlusov.
PY - 2022/2/24
Y1 - 2022/2/24
N2 - 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 μm 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.
AB - 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 μm 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.
KW - cell migration
KW - cell-mediated drug delivery
KW - human adipose-derived mesenchymal stromal/stem cells
KW - synthetic microcapsules
KW - target drug delivery
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U2 - 10.3389/fbioe.2022.796111
DO - 10.3389/fbioe.2022.796111
M3 - Article
AN - SCOPUS:85126203513
SN - 2296-4185
VL - 10
JO - Frontiers in Bioengineering and Biotechnology
JF - Frontiers in Bioengineering and Biotechnology
M1 - 796111
ER -