Iohara Koichiro, Zheng Li, Ito Masataka, Tomokiyo Atsushi, Matsushita Kenji, Nakashima Misako
Laboratory of Oral Disease Research, National Institute for Longevity Sciences, National Center for Geriatrics and Gerontology, Aichi, Japan.
Stem Cells. 2006 Nov;24(11):2493-503. doi: 10.1634/stemcells.2006-0161. Epub 2006 Jul 27.
Dental pulp has the potential to form dentin as a regenerative response to caries. This regeneration is mediated by stem/progenitor cells. Thus, stem cell therapy might be of potential utility in induction of reparative dentin. We isolated side population (SP) cells from dental pulp based on the exclusion of the DNA binding dye Hoechst 33342 by flow cytometry and compared its self-renewal capacities and multipotency with non-SP cells and primary pulp cells. The cumulative cell number of the SP cells was greater than the non-SP cells and primary pulp cells. Bmi1 was continuously expressed in SP cells, suggesting longer proliferative lifespan and self-renewal capacity of SP cells. Next, the maintenance of the multilineage differentiation potential of pulp SP cells was investigated. Expression of type II collagen and aggrecan confirmed chondrogenic conversion (30%) of SP cells. SP cells expressed peroxisome proliferator-activated receptor gamma and adaptor protein 2, showing adipogenic conversion. Expression of mRNA and proteins of neurofilament and neuromodulin confirmed neurogenic conversion (90%). These results demonstrate that pulp SP cells maintain multilineage differentiation potential. We further examined whether bone morphogenetic protein 2 (BMP2) could induce differentiation of pulp SP cells into odontoblasts. BMP2 stimulated the expression of dentin sialophosphoprotein (Dspp) and enamelysin in three-dimensional pellet cultures. Autogenous transplantation of the Bmp2-supplemented SP cells on the amputated pulp stimulated the reparative dentin formation. Thus, adult pulp contains SP cells, which are enriched for stem cell properties and useful for cell therapy with BMP2 for dentin regeneration.
牙髓具有形成牙本质的潜力,作为对龋齿的再生反应。这种再生由干细胞/祖细胞介导。因此,干细胞疗法在诱导修复性牙本质形成方面可能具有潜在效用。我们通过流式细胞术基于DNA结合染料Hoechst 33342的排除从牙髓中分离出侧群(SP)细胞,并将其自我更新能力和多能性与非SP细胞和原代牙髓细胞进行比较。SP细胞的累积细胞数量大于非SP细胞和原代牙髓细胞。Bmi1在SP细胞中持续表达,表明SP细胞具有更长的增殖寿命和自我更新能力。接下来,研究了牙髓SP细胞多谱系分化潜能的维持情况。II型胶原蛋白和聚集蛋白聚糖的表达证实了SP细胞的软骨生成转化(30%)。SP细胞表达过氧化物酶体增殖物激活受体γ和衔接蛋白2,显示出脂肪生成转化。神经丝和神经调节蛋白的mRNA和蛋白质表达证实了神经生成转化(90%)。这些结果表明牙髓SP细胞维持多谱系分化潜能。我们进一步研究了骨形态发生蛋白2(BMP2)是否能诱导牙髓SP细胞分化为成牙本质细胞。BMP2在三维微球培养中刺激了牙本质涎磷蛋白(Dspp)和釉质溶解素的表达。将补充有Bmp2的SP细胞自体移植到截断的牙髓上刺激了修复性牙本质的形成。因此,成人牙髓含有SP细胞,这些细胞富含干细胞特性,对于用BMP2进行牙本质再生的细胞治疗是有用的。