Kawano Shintaro, Morotomi Takahiko, Toyono Takashi, Nakamura Norifumi, Uchida Takashi, Ohishi Masamichi, Toyoshima Kuniaki, Harada Hidemitsu
Department of Oral Anatomy and Cell Biology, Kyushu Dental College, 2-6-1, Manazuru, Kokurakita-ku, Kitakyushu, Japan 803-8580.
Connect Tissue Res. 2002;43(2-3):409-12. doi: 10.1080/03008200290000637.
Rat incisors grow continuously throughout life. Producing a variety of dental epithelial cells is performed by stem cells located in the cervical loop of the incisor apex. To study the mechanisms for cell differentiation, we established a dental epithelial cell line (HAT-7) originating from a cervical loop epithelium of a rat incisor. Immunochemical studies showed that HAT-7 produced the cells expressing amelogenin, ameloblastin, or alkaline phosphatase (ALP). To illustrate a role of Notch signaling in the determinant of the cell fate, we examined expression patterns of Notch1 and Jagged1 in HAT-7 density dependently. At lower cell density, Notch1- or Jagged1-expressing cells were not seen. However, when they were fully confluent, cells began to express Notch1 or Jagged1 strongly. Some ALP-positive cells were almost consistent with Notch1-expressing cells but not Jagged1-expressing cells. These results suggested that the determinant of direction of differentiation was associated with Notch signaling pathway.
大鼠的门牙在其一生中持续生长。位于门牙顶端颈环处的干细胞负责产生多种牙齿上皮细胞。为了研究细胞分化的机制,我们建立了一种源自大鼠门牙颈环上皮的牙齿上皮细胞系(HAT-7)。免疫化学研究表明,HAT-7产生表达釉原蛋白、成釉蛋白或碱性磷酸酶(ALP)的细胞。为了阐明Notch信号在细胞命运决定中的作用,我们检测了HAT-7中Notch1和Jagged1在不同细胞密度下的表达模式。在较低细胞密度时,未观察到表达Notch1或Jagged1的细胞。然而,当细胞完全汇合时,细胞开始强烈表达Notch1或Jagged1。一些ALP阳性细胞几乎与表达Notch1的细胞一致,但与表达Jagged1的细胞不一致。这些结果表明,分化方向的决定与Notch信号通路有关。