Jeon Mijeong, Song Je Seon, Choi Byung-Jai, Choi Hyung-Jun, Shin Dong-Min, Jung Han-Sung, Kim Seong-Oh
Department of Pediatric Dentistry, Oral Science Research Center, College of Dentistry, Yonsei University, Seoul, Republic of Korea.
Department of Oral Biology, College of Dentistry, Yonsei University, Seoul, Republic of Korea.
Arch Oral Biol. 2014 Oct;59(10):1013-23. doi: 10.1016/j.archoralbio.2014.06.002. Epub 2014 Jun 11.
Stem cells from human exfoliated deciduous teeth (SHED) are a good source of dental tissue for regeneration therapy, and can be obtained using different primary culture methods. The aim of this study was to determine the differences in the in vitro and in vivo characteristics between SHED isolated via enzymatic disaggregation (e-SHED) and outgrowth (o-SHED) primary culture methods.
Dental pulp stem cells were isolated from 14 exfoliated deciduous teeth by enzymatic disaggregation (n=7) and outgrowth (n=7). Their proliferation potential and colony-forming ability were evaluated in vitro, as was their mesenchymal stem-cell-marker expression (using flow cytometry), and their differentiation was verified using quantitative real-time PCR (qPCR) and histochemical staining. In addition, the qualitative and quantitative characteristics of the hard tissue that was generated after in vivo transplantation were compared using haematoxylin and eosin staining, immunohistochemical staining, qPCR, and quantitative alkaline phosphatase analysis.
The cell-proliferation potential, colony-forming ability, and Stro-1 and CD146 expression were higher in e-SHED than in o-SHED. While the in vitro adipogenic differentiation potential was greater in e-SHED than in o-SHED, the in vitro osteogenic differentiation did not differ significantly between the two cell types. Although in vivo hard tissue formation was greater following transplantation of o-SHED into mice, there was no difference in the quality of hard tissue generated by e-SHED and o-SHED.
The findings of this study indicate that e-SHED exhibit stronger stemness characteristics, but that o-SHED are more suitable for hard-tissue regeneration therapy in teeth.
人乳牙脱落干细胞(SHED)是用于再生治疗的良好牙组织来源,可通过不同的原代培养方法获得。本研究的目的是确定通过酶解分离(e-SHED)和迁出法(o-SHED)原代培养方法分离的SHED在体外和体内特性上的差异。
通过酶解分离(n = 7)和迁出法(n = 7)从14颗脱落乳牙中分离牙髓干细胞。在体外评估它们的增殖潜力和集落形成能力,以及它们的间充质干细胞标志物表达(使用流式细胞术),并使用定量实时PCR(qPCR)和组织化学染色验证它们的分化。此外,使用苏木精和伊红染色、免疫组织化学染色、qPCR和碱性磷酸酶定量分析比较体内移植后产生的硬组织的定性和定量特征。
e-SHED的细胞增殖潜力、集落形成能力以及Stro-1和CD146表达高于o-SHED。虽然e-SHED的体外成脂分化潜力大于o-SHED,但两种细胞类型之间的体外成骨分化没有显著差异。尽管将o-SHED移植到小鼠体内后体内硬组织形成更多,但e-SHED和o-SHED产生的硬组织质量没有差异。
本研究结果表明,e-SHED表现出更强的干性特征,但o-SHED更适合牙齿的硬组织再生治疗。