Wang Lin, Zhang Chi, Li Chunyan, Weir Michael D, Wang Ping, Reynolds Mark A, Zhao Liang, Xu Hockin H K
VIP Integrated Department, School and Hospital of Stomatology, Jilin University, Changchun, Jilin 130011,China; Department of Endodontics, Periodontics and Prosthodontics, University of Maryland School of Dentistry, Baltimore, MD 21201, USA.
Department of Endodontics, Periodontics and Prosthodontics, University of Maryland School of Dentistry, Baltimore, MD 21201, USA; State Key Laboratory of Oral Diseases, West China School of Stomatology, Sichuan University, Chengdu 610041, China.
Mater Sci Eng C Mater Biol Appl. 2016 Dec 1;69:1125-36. doi: 10.1016/j.msec.2016.08.019. Epub 2016 Aug 10.
Human induced pluripotent stem cell-derived mesenchymal stem cells (hiPSC-MSCs), dental pulp stem cells (hDPSCs) and bone marrow MSCs (hBMSCs) are exciting cell sources in regenerative medicine. However, there has been no report comparing hDPSCs, hBMSCs and hiPSC-MSCs for bone engineering in an injectable calcium phosphate cement (CPC) scaffold. The objectives of this study were to: (1) develop a novel injectable CPC containing hydrogel fibers encapsulating stem cells for bone engineering, and (2) compare cell viability, proliferation and osteogenic differentiation of hDPSCs, hiPSC-MSCs from bone marrow (BM-hiPSC-MSCs) and from foreskin (FS-hiPSC-MSCs), and hBMSCs in CPC for the first time. The results showed that the injection did not harm cell viability. The porosity of injectable CPC was 62%. All four types of cells proliferated and differentiated down the osteogenic lineage inside hydrogel fibers in CPC. hDPSCs, BM-hiPSC-MSCs, and hBMSCs exhibited high alkaline phosphatase, runt-related transcription factor, collagen I, and osteocalcin gene expressions. Cell-synthesized minerals increased with time (p<0.05), with no significant difference among hDPSCs, BM-hiPSC-MSCs and hBMSCs (p>0.1). Mineralization by hDPSCs, BM-hiPSC-MSCs, and hBMSCs inside CPC at 14d was 14-fold that at 1d. FS-hiPSC-MSCs were inferior in osteogenic differentiation compared to the other cells. In conclusion, hDPSCs, BM-hiPSC-MSCs and hBMSCs are similarly and highly promising for bone tissue engineering; however, FS-hiPSC-MSCs were relatively inferior in osteogenesis. The novel injectable CPC with cell-encapsulating hydrogel fibers may enhance bone regeneration in dental, craniofacial and orthopedic applications.
人诱导多能干细胞来源的间充质干细胞(hiPSC-MSCs)、牙髓干细胞(hDPSCs)和骨髓间充质干细胞(hBMSCs)是再生医学中令人兴奋的细胞来源。然而,尚无关于在可注射磷酸钙骨水泥(CPC)支架中比较hDPSCs、hBMSCs和hiPSC-MSCs用于骨工程的报道。本研究的目的是:(1)开发一种新型的可注射CPC,其包含包裹干细胞的水凝胶纤维用于骨工程,以及(2)首次比较hDPSCs、来自骨髓的hiPSC-MSCs(BM-hiPSC-MSCs)、来自包皮的hiPSC-MSCs(FS-hiPSC-MSCs)和hBMSCs在CPC中的细胞活力、增殖和成骨分化。结果表明,注射不会损害细胞活力。可注射CPC的孔隙率为62%。所有四种类型的细胞在CPC的水凝胶纤维内增殖并沿成骨谱系分化。hDPSCs、BM-hiPSC-MSCs和hBMSCs表现出高碱性磷酸酶、 runt相关转录因子、I型胶原蛋白和骨钙素基因表达。细胞合成的矿物质随时间增加(p<0.05),hDPSCs、BM-hiPSC-MSCs和hBMSCs之间无显著差异(p>0.1)。14天时,hDPSCs、BM-hiPSC-MSCs和hBMSCs在CPC内的矿化是1天时的14倍。与其他细胞相比,FS-hiPSC-MSCs的成骨分化较差。总之,hDPSCs、BM-hiPSC-MSCs和hBMSCs在骨组织工程方面同样具有很高的前景;然而,FS-hiPSC-MSCs在成骨方面相对较差。具有包裹细胞的水凝胶纤维的新型可注射CPC可能会增强牙科、颅面和骨科应用中的骨再生。