Effects of extracellular calcium on viability and osteogenic differentiation of bone marrow stromal cells in vitro

被引:29
作者
Cheng, Shaowen [1 ]
Wang, Wei [2 ]
Lin, Zhongqin [3 ]
Zhou, Ping [4 ]
Zhang, Xiaolei [2 ]
Zhang, Wei [2 ]
Chen, Qingyu [2 ]
Kou, Dongquan [2 ]
Ying, Xiaozhou [2 ]
Shen, Yue [2 ]
Cheng, Xiaojie [2 ]
Yu, Ziming [1 ]
Peng, Lei [1 ]
Lu, Chuanzhu [1 ]
机构
[1] Hainan Med Coll, Affiliated Hosp, Ctr Trauma, Haikou 571100, Peoples R China
[2] Wenzhou Med Coll, Affiliated Hosp 2, Dept Orthopaed Surg, Wenzhou 325000, Peoples R China
[3] Hosp Integrated Tradit Chinese & Western Med Wenz, Dept Orthopaed Surg, Wenzhou, Peoples R China
[4] Zhejiang Univ, Affiliated Hosp 1, Dept Oncol, Hangzhou 310003, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Mesenchymal stem cell; Osteogenesis; Calcium; Viability; Differentiation; MESENCHYMAL STEM-CELLS; OSTEOBLAST PROLIFERATION; GENE-EXPRESSION; DEFECTS; MATRIX; REPAIR; HYDROXYAPATITE; OSTEOPONTIN; OSTEOCALCIN; PHOSPHATE;
D O I
10.1007/s13577-012-0041-8
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Bone marrow stromal cells (BMSCs) have been extensively used for tissue engineering. However, the effect of Ca2+ on the viability and osteogenic differentiation of BMSCs has yet to be evaluated. To determine the dose-dependent effect of Ca2+ on viability and osteogenesis of BMSCs in vitro, BMSCs were cultured in calcium-free DMEM medium supplemented with various concentrations of Ca2+ (0, 1, 2, 3, 4, and 5 mM) from calcium citrate. Cell viability was analyzed by MTT assay and osteogenic differentiation was evaluated by alkaline phosphatase (ALP) assay, Von Kossa staining, and real-time PCR. Ca2+ stimulated BMSCs viability in a dose-dependent manner. At slightly higher concentrations (4 and 5 mM) in the culture, Ca2+ significantly inhibited the activity of ALP on days 7 and 14 (P < 0.01 or P < 0.05), significantly suppressed collagen synthesis (P < 0.01 or P < 0.05), and significantly elevated calcium deposition (P < 0.01) and mRNA levels of osteocalcin (P < 0.01 or P < 0.05) and osteopontin (P < 0.01 or P < 0.05). Therefore, elevated concentrations of extracellular calcium may promote cell viability and late-stage osteogenic differentiation, but may suppress early-stage osteogenic differentiation in BMSCs.
引用
收藏
页码:114 / 120
页数:7
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