ВлиÑние криоконÑÐµÑ€Ð²Ð¸Ñ€Ð¾Ð²Ð°Ð½Ð¸Ñ Ð½Ð° жизнеÑпоÑобноÑть, иммунофенотип и дифференцировочные ÑвойÑтва мезенхимальных Ñтромальных клеток ранних Ñтадий органогенеза
The effect of cryopreservation by slow program cooling on the viability, immunophenotypic and differentiative properties of mesenchymal stromal cells (MSCs) of early organogenesis stage was studied. It was shown that after cryopreservation under the protection of 10% dimethyl sulfoxide (Me2SO) at th...
Saved in:
Date: | 2010 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Published: |
Publishing House ‘Akademperiodyka’ of the National Academy of Sciences of Ukraine; Institute for Problems of Cryobiology and Cryomedicine
2010
|
Subjects: | |
Online Access: | https://cryo.org.ua/journal/index.php/probl-cryobiol-cryomed/article/view/202 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Journal Title: | Problems of Cryobiology and Cryomedicine |
Institution
Problems of Cryobiology and CryomedicineSummary: | The effect of cryopreservation by slow program cooling on the viability, immunophenotypic and differentiative properties of mesenchymal stromal cells (MSCs) of early organogenesis stage was studied. It was shown that after cryopreservation under the protection of 10% dimethyl sulfoxide (Me2SO) at the cooling rate of 1°C/min down to –80°C with the following plunging into liquid nitrogen the cell viability assessed by trypan blue staining was 88.4 ± 1.7%. The metabolic activity of cells assessed by Alamar Blue reduction assay decreased after cryopreservation by 15%. Immunophenotypic analysis of MSCs after 4–12 passages showed that 95% of cells expressed the markers CD29, CD44, CD73, CD105 prior to and after cryopreservation. The number of CD34–, CD38– and CD45– cells was more than 95%. After cryopreservation MSCs maintained their capacity for induced differentiation into osteogenic and adipogenic directions. Slow cooling with Me2SO as cryoprotectant was observed to stimulate differentiation of MSCs. |
---|