Couve E, Osorio R, Schmachtenberg O
Instituto de Biología, Laboratorio de Microscopía Electrónica Centro Interdisciplinario de Neurociencia de Valparaíso Facultad de Ciencias, Universidad de Valparaíso, Valparaíso, Chile
Instituto de Biología, Laboratorio de Microscopía Electrónica Facultad de Ciencias, Universidad de Valparaíso, Valparaíso, Chile.
J Dent Res. 2014 Aug;93(8):788-93. doi: 10.1177/0022034514539507. Epub 2014 Jun 13.
Reactionary dentin formation is an adaptive secretory response mediated by odontoblasts to moderate dentin injury. The implications of this process for neuroimmune interactions operating to contain pathogens have not been fully appreciated. The purpose of the present study was to describe the relationship between reactionary dentinogenesis, the neurogenic changes of dental pulp innervation, and dendritic cell recruitment to caries progression, using a comparative immunohistochemical approach in human teeth from young adult individuals. Reactionary dentin formation during dentin caries progression is associated with changes in the integrity of junctional complexes within the odontoblast layer. Diminished coexpression of Cx43 and zonula occludens 1 implies a reduced level of intercellular connectivity between odontoblasts. Dentin caries also causes overexpression of growth-associated protein 43, a modulator of neural plasticity that promotes extensive sprouting of nerve endings into the reactionary dentin matrix. At the same time, an elevated number of HLA-DR-positive dendritic cells infiltrate the odontoblast layer and subsequently invade reactionary dentin formed underneath the early caries-affected regions. Simultaneous odontoblast layer remodeling, nerve fiber sprouting, and activation of dendritic cells during caries progression suggest a coordinated neuroimmune response to fight caries pathogen invasion and to promote dentin-pulp healing. We propose that reactionary dentin formation hinders pathogen invasion and supports defensive neuroimmune interactions against infection. The eventual understanding of this complex scenario may contribute to the development of novel approaches to dental caries treatment.
反应性牙本质形成是成牙本质细胞介导的一种适应性分泌反应,以适度应对牙本质损伤。这一过程对于控制病原体的神经免疫相互作用的影响尚未得到充分认识。本研究的目的是使用比较免疫组织化学方法,描述年轻成年个体人牙中反应性牙本质形成、牙髓神经支配的神经源性变化与树突状细胞募集到龋病进展之间的关系。牙本质龋进展过程中的反应性牙本质形成与成牙本质细胞层内连接复合体完整性的变化有关。Cx43和紧密连接蛋白1的共表达减少意味着成牙本质细胞之间的细胞间连接水平降低。牙本质龋还会导致生长相关蛋白43的过度表达,该蛋白是一种神经可塑性调节剂,可促进神经末梢广泛向反应性牙本质基质中芽生。同时,大量HLA-DR阳性树突状细胞浸润成牙本质细胞层,并随后侵入早期龋损区域下方形成的反应性牙本质。龋病进展过程中同时发生的成牙本质细胞层重塑、神经纤维芽生和树突状细胞激活表明存在一种协调的神经免疫反应,以对抗龋病病原体入侵并促进牙本质-牙髓愈合。我们提出,反应性牙本质形成可阻碍病原体入侵,并支持针对感染的防御性神经免疫相互作用。最终理解这一复杂情况可能有助于开发新的龋齿治疗方法。