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Merck
  • The influence of scaffold microstructure on chondrogenic differentiation of mesenchymal stem cells.

The influence of scaffold microstructure on chondrogenic differentiation of mesenchymal stem cells.

Biomedical materials (Bristol, England) (2014-05-14)
Jingjing Zhang, Yingnan Wu, Tanushree Thote, Eng Hin Lee, Zigang Ge, Zheng Yang
摘要

Different forms of biomaterials, including microspheres, sponges, hydrogels and nanofibres have been broadly used in cartilage regeneration; however, effects of internal structures of biomaterials on chondrogenesis of mesenchymal stem cells (MSCs) remain largely unexplored. Here we investigated the effect of physical microenvironments of sponges and hydrogels on chondrogenic differentiation of MSCs. MSCs, cultured in these two scaffold systems, were induced with TGF-β3 in chondrogeneic differentiation medium and the chondrogenic differentiation was evaluated and compared after three weeks. MSCs in the sponges clustered with spindle morphologies, while they distributed homogenously with round morphologies in the hydrogel. The MSCs proliferated faster in the sponge compared to that in the hydrogel. Significantly higher glycosaminoglycan and collagen II were found in the sponges but not in the hydrogels. The different tissue formation ability of MSCs in these two systems could be attributed to the different metabolic requirements and the cellular events prerequisite in the chondrogenic process of MSCs. It is reasonable to conclude that sponges with relatively active microenvironments that facilitate cell-cell contacts and cell-matrix interaction are optimal for early stage of chondrogeneic differentiation.

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Sigma-Aldrich
地塞米松, powder, BioReagent, suitable for cell culture, ≥97%
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DAPI, for nucleic acid staining
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噻唑蓝, 98%
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碘化丙啶, ≥94.0% (HPLC)
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丙酮酸钠, powder, BioReagent, suitable for cell culture, suitable for insect cell culture, ≥99%
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丙酮酸钠, ReagentPlus®, ≥99%
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荧光素二乙酸盐, used as cell viability stain
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丙酮酸钠, Hybri-Max, powder, suitable for hybridoma
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丙酮酸钠, powder, BioXtra, suitable for mouse embryo cell culture
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