Proliferation capacity and viability of adipose-derived stromal cells labeled with ultrasmall superparamagnetic particles of iron oxide
10.3760/cma.j.issn.1671-8925.2012.05.003
- VernacularTitle:超小超顺磁氧化铁颗粒标记对脂肪源间充质干细胞生物学特性的影响
- Author:
Chen YAO
1
;
Yan-Wu GUO
;
Ming LI
;
Qiang CHEN
;
Feng-Fei LU
;
Guo-Hui LU
;
Shi-Zhong ZHANG
;
Xiao-Dan JIANG
Author Information
1. 南方医科大学珠江医院
- Keywords:
Adipose-derived stromal cell;
Ultrasmall superparamagnetic particle of iron oxide;
Viability
- From:
Chinese Journal of Neuromedicine
2012;11(5):443-447
- CountryChina
- Language:Chinese
-
Abstract:
Objective To label adipose-derived stromal cells (ADSCs) with different concentrations of ultrasmall superparamagnetic particles of iron oxide (USPIO) to investigate the biological characteristics of ADSCs treated with these USPIO,and determine the optimal concentration of USPIO in labeling ADSCs in vitro. Methods USPIO with different concentrations were prepared,and the particles were endocytosed by ADSCs generated from rat adipose tissue. Eight groups (negative control group,blank control group,and 11.25,22.5,45,90,135 and 180 μg/mL treatment groups) were chosen. Labeling efficiency and cellular uptake were analyzed by Prussian blue staining. Meanwhile,proliferation capacity and viability of ADSCs were evaluated by Alamar blue assay and Cell Counting kit-8. Results ADSCs could be effectively labeled with USPIO: approximately 95％ ADSCs were labeled when they were incubated with USPIO for 24 h under the concentration of USPIO was 45 μg/mL;and approximately 100％ ADSCs were labeled when the concentration of USPIO was 90 μg/mL and above. The CCK-8 and Alamar blue tests showed that USPIO of different concentrations (11.25-90 μg/mL) had little influence on cell growth viability,and no significant difference was noted between each 2 concentration groups (P＞0.05). In a word, 45-90 μg/mL USPIO were the optimal choice for transplantion of ADSCs in vivo. Conclusion ADSCs from the adipose tissue can be effectively labeled with USPIO with minimal effect on cell proliferation and viability.
