The effects of low intensity pulsed ultrasound on the proliferation and osteogenic differentiation of rat adipose tissue-derived stem cells
10.3760/cma.j.issn.0254-1424.2011.06.004
- VernacularTitle:低强度脉冲超声波对大鼠脂肪干细胞增殖及成骨分化的影响
- Author:
Ting JIANG
;
Fengjing GUO
;
Tao XU
;
Keqing YANG
- Publication Type:Journal Article
- Keywords:
Low intensity pulsed ultrasound;
Rats;
Adipose tissue-derived stem cells;
Proliferation;
Osteogenic differentiation
- From:
Chinese Journal of Physical Medicine and Rehabilitation
2011;33(6):408-412
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the biological effects of low intensity pulsed ultrasound (LIPUS) on the proliferation and osteogenic differentiation of adipose tissue-derived stem cells (ADSCs) in vitro.Methods Primary ADSCs were harvested from the inguinal fat pads of 4-week-old female Sprague-Dawley rats,cultured in vitro and purified by magnetic-activated cell sorting.Surface ADSC markers were identified by flow cytometry.LIPUS at 100 mW/cm2 was used to stimulate the cultured cells.Flow cytometry was performed for cell cycle analysis.Cellular proliferation was evaluated via CCK8 chromatometry,and a proliferation index was calculated.ADSCs were assigned to 4 groups:a negative control group,a LIPUS group,an osteoinduction group and a LIPUS plus osteoinduction group,and treated accordingly.Alkaline phosphatase (ALP) activity was determined at the 7th and 14th day in each group,and calcium nodes were marked by Von Kossa staining.The levels of osteogenic differentiation in the different groups were evaluated.Results The ADSCs of passage 3 expressed CD 34low,and CD29high CD44high,which was consistent with the characteristics of ADSC surface markers.Proliferation was upregulated significantly in the LIPUS group compared with the negative control group.ALP activity was also elevated significantly and it resulted in mine-ralization.The highest mineralization rate was observed in the LIPUS plus osteoinduction group.Conclusions LIPUS not only can stimulate the proliferation of rat ADSCs,it also promotes their osteogenic differentiation.
