Self-Assembling Peptide Amphiphile Nanofibers as a Scaffold for Dental Stem Cells

被引:120
作者
Galler, Kerstin M. [1 ,2 ,3 ,4 ]
Cavender, Adriana [3 ]
Yuwono, Virany [1 ,2 ]
Dong, He [1 ,2 ]
Shi, Songtao [5 ]
Schmalz, Gottfried [4 ]
Hartgerink, Jeffrey D. [1 ,2 ]
D'Souza, Rena N. [3 ]
机构
[1] Rice Univ, Dept Chem, Houston, TX 77005 USA
[2] Rice Univ, Dept Bioengn, Houston, TX 77005 USA
[3] Baylor Coll Dent, Dept Biomed Sci, TAMUHSC, Dallas, TX 75246 USA
[4] Univ Regensburg, Dept Operat Dent, Regensburg, Germany
[5] Univ So Calif, Ctr Craniofacial Mol Biol, Sch Dent, Los Angeles, CA 90033 USA
关键词
D O I
10.1089/ten.tea.2007.0413
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Dental caries remains one of the most prevalent infectious diseases in the world. So far, available treatment methods rely on the replacement of decayed soft and mineralized tissue with inert biomaterials alone. As an approach to develop novel regenerative strategies and engineer dental tissues, two dental stem cell lines were combined with peptide-amphiphile (PA) hydrogel scaffolds. PAs self-assemble into three-dimensional networks of nanofibers, and living cells can be encapsulated. Cell-matrix interactions were tailored by incorporation of the cell adhesion sequence RGD and an enzyme-cleavable site. SHED (stem cells from human exfoliated deciduous teeth) and DPSC (dental pulp stem cells) were cultured in PA hydrogels for 4 weeks using different osteogenic supplements. Both cell lines proliferate and differentiate within the hydrogels. Histologic analysis shows degradation of the gels and extracellular matrix production. However, distinct differences between the two cell lines can be observed. SHED show a spindle-shaped morphology, high proliferation rates, and collagen production, resulting in soft tissue formation. In contrast, DPSC reduce proliferation, but exhibit an osteoblast-like phenotype, express osteoblast marker genes, and deposit mineral. Since the hydrogels are easy to handle and can be introduced into small defects, this novel system might be suitable for engineering both soft and mineralized matrices for dental tissue regeneration.
引用
收藏
页码:2051 / 2058
页数:8
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