Pluronic F-127 hydrogel as a promising scaffold for encapsulation of dental-derived mesenchymal stem cells

被引:165
作者
Diniz, Ivana M. A. [1 ,2 ]
Chen, Chider [1 ]
Xu, Xingtian [1 ]
Ansari, Sahar [1 ,3 ]
Zadeh, Homayoun H. [3 ]
Marques, Marcia M. [2 ]
Shi, Songtao [1 ]
Moshaverinia, Alireza [1 ]
机构
[1] Univ So Calif, Ostrow Sch Dent USC, Ctr Craniofacial Mol Biol, Los Angeles, CA 90033 USA
[2] Univ Sao Paulo, Sch Dent, Dept Restorat Dent, Sao Paulo, Brazil
[3] Univ So Calif, Ostrow Sch Dent USC, Lab Immunoregulat & Tissue Engn LITE, Los Angeles, CA 90033 USA
基金
巴西圣保罗研究基金会;
关键词
GINGIVAL TISSUE SOURCES; PERIODONTAL-LIGAMENT; ALGINATE HYDROGEL; BONE REGENERATION; F127; HYDROGEL; IN-VITRO; DIFFERENTIATION; CARTILAGE; VIVO; SKIN;
D O I
10.1007/s10856-015-5493-4
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Dental-derived mesenchymal stem cells (MSCs) provide an advantageous therapeutic option for tissue engineering due to their high accessibility and bioavailability. However, delivering MSCs to defect sites while maintaining a high MSC survival rate is still a critical challenge in MSC-mediated tissue regeneration. Here, we tested the osteogenic and adipogenic differentiation capacity of dental pulp stem cells (DPSCs) in a thermoreversible Pluronic F127 hydrogel scaffold encapsulation system in vitro. DPSCs were encapsulated in Pluronic (R) F-127 hydrogel and stem cell viability, proliferation and differentiation into adipogenic and osteogenic tissues were evaluated. The degradation profile and swelling kinetics of the hydrogel were also analyzed. Our results confirmed that Pluronic F-127 is a promising and nontoxic scaffold for encapsulation of DPSCs as well as control human bone marrow MSCs (hBMMSCs), yielding high stem cell viability and proliferation. Moreover, after 2 weeks of differentiation in vitro, DPSCs as well as hBMMSCs exhibited high levels of mRNA expression for osteogenic and adipogenic gene markers via PCR analysis. Our histochemical staining further confirmed the ability of Pluronic F-127 to direct the differentiation of these stem cells into osteogenic and adipogenic tissues. Furthermore, our results revealed that Pluronic F-127 has a dense tubular and reticular network morphology, which contributes to its high permeability and solubility, consistent with its high degradability in the tested conditions. Altogether, our findings demonstrate that Pluronic F-127 is a promising scaffold for encapsulation of DPSCs and can be considered for cell delivery purposes in tissue engineering.
引用
收藏
页码:1 / 10
页数:10
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