Potent Osteogenesis and Chondrogenesis of CD34-Enriched Mouse Adipose-Derived Stem Cells

被引:1
作者
Xiong, Yao [1 ,3 ]
He, Jing [2 ]
Zhang, Wenjie [1 ,3 ]
Zhou, Guangdong [1 ,3 ]
Cao, Yilin [1 ,3 ]
Liu, Wei [1 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai People Hosp 9, Dept Plast & Reconstruct Surg,Shanghai Key Lab Ti, Shanghai 200011, Peoples R China
[2] Tongji Univ, Sch Med, Dept Anat & Neurobiol, Shanghai 200092, Peoples R China
[3] Natl Tissue Engn Ctr China, Shanghai 200041, Peoples R China
基金
中国国家自然科学基金;
关键词
Adipose-derived stem cells (ASCs); Adipose-derived mesenchymal stem cells (ADMSCs); Mucosialin (CD34); Cell sorting; Osteogenesis; Chondrogenesis; MARROW STROMAL CELLS; HUMAN BONE-MARROW; IN-VIVO; TRICALCIUM PHOSPHATE; PROGENITOR CELLS; TISSUE; DEFECT; HYDROXYAPATITE; CONSTRUCTS; THERAPIES;
D O I
10.5405/jmbe.1581
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Adipose-derived stem cells (ASCs) obtained using a widely reported culture method are actually a heterozygous cell population of the adipose stromal vascular fraction (SVF). This heterogeneity may interfere with the multi-differentiation potential of adipose-derived mesenchymal stem cells (ADMSCs). It is therefore necessary to establish an efficient method for isolating ADMSCs that have high multi-differentiation potential. Several studies indicated that mucosialin (CD34) might be one of the specific markers of ADMSCs. In our previous studies, a CD34-enriched cell population sorted from the pooled SVF had stronger differentiation potential than that of unsorted cells in a hair follicle morphogenesis model. However, it remains unclear whether CD34-enriched cells have stronger potential for other lineage differentiation, particularly osteogenesis and chondrogenesis. In this study, CD34(+) cells were harvested and sorted from murine adipose-derived cells and their potentials for osteogenesis and chondrogesis were examined using engineered bone and cartilage models. The results show that CD34(+) cells exhibited stronger potential for bone formation with stronger van Gieson and collagen I staining than those of CD34(-) cells and an unsorted SVF when seeded on beta-tricalcium phosphate. Furthermore, CD34(+) cells also exhibited a much stronger chondrogenic potential than those of CD34(-) cells and an unsorted SVF, with stronger staining of toluidine blue, Safranin-O, and collagen II in a chondrocyte pellet and engineered cartilage. Most importantly, only CD34(+) cells could form a cartilage-like lacunae structure. All these results indicate that CD34(-) may serve as a specific surface marker for enriching ADMSCs in ASCs.
引用
收藏
页码:230 / 237
页数:8
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