Effect of water-soluble P-chitosan and S-chitosan on human primary osteoblasts and giant cell tumor of bone stromal cells

被引:19
作者
Tang, T. [1 ]
Zhang, G. [1 ]
Lau, Carol P. Y. [1 ]
Zheng, L. Z. [1 ]
Xie, X. H. [1 ]
Wang, X. L. [1 ]
Wang, X. H. [2 ]
He, K. [2 ]
Patrick, Y. [1 ]
Qin, L. [1 ,3 ]
Kumta, Shekhar M. [1 ]
机构
[1] Chinese Univ Hong Kong, Dept Orthopaed & Traumatol, Hong Kong, Hong Kong, Peoples R China
[2] Tsinghua Univ, Dept Mech Engn, Inst Biomfg Engn, Beijing 100084, Peoples R China
[3] Chinese Acad Sci, Translat Med Res & Dev Ctr, Inst Biomed & Hlth Engn, Shenzhen Inst Adv Technol, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
EPITHELIUM-DERIVED FACTOR; CALCIUM-PHOSPHATE CEMENTS; PHOSPHORYLATED CHITOSAN; CHITIN; RECONSTRUCTION; DERIVATIVES; RABBITS; GROWTH; REPAIR;
D O I
10.1088/1748-6041/6/1/015004
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Water-soluble phosphorylated chitosan (P-chitosan) and disodium (1 -> 4)-2-deoxy-2-sulfoamino-beta-D-glucopyranuronan (S-chitosan) are two chemically modified chitosans. In this study, we found that P-chitosan significantly promotes cell proliferation of both human primary osteoblasts (OBs) and the OB like stromal cell component of the giant cell tumor of bone (GCTB) cells at the concentration from 125 to 1000 mu g ml(-1) at all time points of 1, 3, 5 and 7 days after treatment. Further investigation of the osteogenic effect of the P-chitosan suggested that it regulates the levels of osteoclastogenic factors, receptor activator of nuclear factor kappa B ligand and osteoprotegerin expression. An interesting finding is that S-chitosan at lower concentration (100 mu g ml (1)) stimulates cell proliferation while a higher dose (1000 mu g ml(-1)) of S-chitosan inhibits it. The inhibitory effect of S-chitosan on human primary GCT stromal cells was greater than that of OBs (p < 0.05). Taken together, our findings elucidated the osteogenic effect of P-chitosan and the varying effects of S-chitosan on the proliferation of human primary OBs and GCT stromal cells and provided us the rationale for the construction of novel bone repair biomaterials with the dual properties of bone induction and bone tumor inhibition.
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页数:9
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