Yang Jing-Wen, Zhang Yu-Feng, Sun Zhe-Yi, Song Guang-Tai, Chen Zhi
The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) & Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan University, Wuhan, PR China.
The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) & Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan University, Wuhan, PR China
J Biomater Appl. 2015 Aug;30(2):221-9. doi: 10.1177/0885328215577296. Epub 2015 Mar 18.
The clinical translation of regenerative endodontics demands further development of suitable scaffolds. Here, we assessed the possibility of using silk fibroin scaffold for pulp regeneration with dental pulp stem cells (DPSCs) and basic fibroblast growth factor (bFGF) in ectopic root canal transplantation model. Porous silk fibroin scaffolds were fabricated using freeze-drying technique (with or without bFGF incorporation), and characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy. DPSCs were isolated, characterized, seeded onto scaffolds, and inserted into the tooth root fragments. Cell viability and morphology were tested in the 3D model in vitro using CCK8 assay and SEM. Furthermore, the ectopic transplantation model was used to verify the generation of pulp-like tissue in DPSCs seeded silk fibroin scaffold with bFGF, as examined by histological analysis. DPSCs seeded in silk fibroin scaffold survived, exhibited cytoplasmic elongation in scaffolds at least 4 weeks in culture. bFGF promoted DPSCs viability in tooth fragments/scaffolds (TSS) between 7 and 28 days. Pulp-like tissue was generated in the bFGF-incorporated TSS with DPSCs. Histologically, the generated tissue was shown to be with well vascularity, have new matrix deposition and dentin-like tissue formation, and consist of both the transplanted and host-derived cells. Collectively, these data support the use of bFGF-incorporated silk fibroin scaffold as a highly promising scaffold candidate for future treatment concepts in regenerative endodontics to save teeth.
再生牙髓治疗的临床转化需要进一步开发合适的支架。在此,我们评估了在异位根管移植模型中使用丝素蛋白支架与牙髓干细胞(DPSCs)和碱性成纤维细胞生长因子(bFGF)进行牙髓再生的可能性。使用冷冻干燥技术制备多孔丝素蛋白支架(含或不含bFGF),并通过扫描电子显微镜(SEM)和傅里叶变换红外光谱进行表征。分离、鉴定DPSCs,将其接种到支架上,并插入牙根片段中。使用CCK8测定法和SEM在体外3D模型中测试细胞活力和形态。此外,通过组织学分析,使用异位移植模型验证接种DPSCs的含bFGF丝素蛋白支架中牙髓样组织的生成情况。接种在丝素蛋白支架中的DPSCs存活,在培养至少4周的支架中表现出细胞质伸长。bFGF在7至28天内促进了DPSCs在牙片段/支架(TSS)中的活力。在含bFGF且接种DPSCs的TSS中生成了牙髓样组织。组织学上,生成的组织显示血管丰富,有新的基质沉积和牙本质样组织形成,并且由移植细胞和宿主来源的细胞组成。总体而言,这些数据支持使用含bFGF的丝素蛋白支架作为再生牙髓治疗未来治疗理念中极具前景的支架候选物以保存牙齿。