Oyama M, Myokai F, Ohira T, Shiomi N, Yamashiro K, Arai H, Nishimura F, Takashiba S
Department of Pathophysiology-Periodontal Science, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, 2-5-1 Shikatacho, Okayama, 700-8525, Japan.
J Dent Res. 2005 Sep;84(9):842-7. doi: 10.1177/154405910508400912.
Pulpal wound healing followed by cavity preparation may involve reactionary or reparative dentinogenesis in relation to the cavity position; however, little is known about the molecular responses. We aimed to isolate and analyze genes induced or suppressed in the wounded pulp to identify molecular processes involved in the pulp responses to injury. Twenty-three cDNAs were isolated by cDNA subtraction between healthy and wounded pulp of rats. By library screening, we identified rat 14.7K-interacting protein (rFIP)-2A and B genes homologous to human FIP-2, being involved in regulating membrane trafficking and cellular morphogenesis. RT-PCR analysis showed induction for only rFIP-2B in the wounded pulp. In situ hybridization analysis revealed that both rFIP-2s were expressed strongly in condensing mesenchymal cells of the palatal process and surrounding Meckel's cartilage, but not in intramembranous chondrogenic cells. Thus, up-regulated rFIP-2B expression may play a role in regulating membrane trafficking or cellular morphogenesis of these embryonic and wounded pulpal cells.
牙髓损伤愈合后进行窝洞预备,可能会根据窝洞位置出现反应性或修复性牙本质形成;然而,关于分子反应却知之甚少。我们旨在分离并分析损伤牙髓中诱导或抑制的基因,以确定牙髓对损伤反应所涉及的分子过程。通过大鼠健康牙髓与损伤牙髓之间的cDNA消减杂交技术,分离出23个cDNA。通过文库筛选,我们鉴定出与人类FIP-2同源的大鼠14.7K相互作用蛋白(rFIP)-2A和B基因,它们参与调节膜转运和细胞形态发生。RT-PCR分析显示,损伤牙髓中仅rFIP-2B被诱导。原位杂交分析表明,两种rFIP-2在腭突的凝聚间充质细胞和周围的梅克尔软骨中强烈表达,但在膜内软骨生成细胞中不表达。因此,上调的rFIP-2B表达可能在调节这些胚胎和损伤牙髓细胞的膜转运或细胞形态发生中发挥作用。