Loading…

Effect of Non-Thermal Plasma on Proliferative Activity and Adhesion of Multipotent Stromal Cells to Scaffolds Developed for Tissue-Engineered Constructs

We studied the effect of non-thermal argon plasma on proliferative activity of bone marrow multipotent stromal cells in vitro . Treatment of stromal cell suspension with pure argon did not affect their proliferation. The cells treated with non-thermal argon plasma and explanted in the treatment medi...

Full description

Saved in:
Bibliographic Details
Published in:Bulletin of experimental biology and medicine 2019-05, Vol.167 (1), p.182-188
Main Authors: Chailakhyan, R. K., Grosheva, A. G., Gerasimov, Yu. V., Vorob’eva, N. N., Ermolaeva, S. A., Sysolyatina, E. V., Kazakova, M. V., Akishev, Yu. S., Petryakov, A. V., Sidoruk, K. V., Burdukovskii, V. F., Timashev, P. S.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:We studied the effect of non-thermal argon plasma on proliferative activity of bone marrow multipotent stromal cells in vitro . Treatment of stromal cell suspension with pure argon did not affect their proliferation. The cells treated with non-thermal argon plasma and explanted in the treatment medium demonstrated growth inhibition by 30-40% in comparison with the control. Multipotent stromal cells treated with plasma and after centrifugation explanted in normal medium within 12 min demonstrated accelerated growth. The total cell growth from the pellet and supernatant significantly exceeded the control values. We also analyzed adhesion and proliferative activity of multipotent stromal cells treated with non-thermal plasma on bioresorbable carriers. The cells adhered and proliferated on all types of studied samples. Adhesion properties of scaffolds differed. Caprolactone was found to be the most suitable material for adhesion and proliferation of multipotent stromal cells.
ISSN:0007-4888
1573-8221
DOI:10.1007/s10517-019-04486-0