HUANG Hong,ZHU Fang-qiang,SUN Hong-zhen,FENG Shuai-nan,WANG Zheng-guo,ZHU Pei-fang,ZHANG Bo.Differentiation of swine adipose tissue-derived stromal cells into adipocytes and osteoblasts in vitro[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(13):1219-1222.
HUANG Hong,ZHU Fang-qiang,SUN Hong-zhen,FENG Shuai-nan,WANG Zheng-guo,ZHU Pei-fang,ZHANG Bo.Differentiation of swine adipose tissue-derived stromal cells into adipocytes and osteoblasts in vitro[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(13):1219-1222.DOI:
Differentiation of swine adipose tissue-derived stromal cells into adipocytes and osteoblasts in vitro
Objective To investigate the multilineage differentiation capacity of mesenchymal stem cells isolated and cultured from swine adipose tissue. Methods Adipose tissue-derived stromal cells (ADSCs) were obtained from adipose tissue of swine abdominal wall. The cells presented fibroblast-like in the culture medium. Adipose tissue was minced and digested with collagenase type Ⅰ. The obtained cells were plated and expanded in DMEM/F12 medium. Then the cells were cultivated in osteoblast-inducing culture medium
and osteoblast phenotype was assayed with Gomori and von Kossa staining. The passage cells were cultured in adipogenisis medium and stained with Oil Red O for identification. The cells were observed with inverted microscope each day. Results ADSCs grew as adherent cells and presented fibroblast-like in vitro
and could stably proliferate and be passed. Polygon-shaped cells were characterized by large size with a relatively large nucleus and plenty of cytoplasm after osteoblast-inducing. The cells changed from fibroblast-like into ellipse after adipogenisis-inducing cultivation. There were a lot of alkaline phosphatase (ALP) particles by Gomori staining. After induced for 15 and 19 d
positive cells for ALP were (25.0±7.5)%and (49.7±6.9)%
respectively. Von Kossa staining demonstrated the formation of mineralized nods in extracellular matrix. Under the inverted microscope
there existed significant lipid drops around the cell nucleus after adipogenisis-inducing cultivation for 2 d. The adipocytes rate on day 3
7 and 14 was (22.3±12.5)%
(49.6±7.1)% and (89.4±9.3)%
respectively. After 14 d of adipocyte inducing
about (92.5±9.1)% cells displayed accumulation of lipid vacuoles
as detected by Red Oil O. Conclusion ADSCs isolated and cultured from swine adipose tissue can be induced to be osteo-inducing and adipogenisis
suggesting that the cells have the multilineage differentiation.