Song Minju, Kim Sol, Kim Terresa, Park Sil, Shin Ki-Hyuk, Kang Mo, Park No-Hee, Kim Reuben
The Shapiro Family Laboratory of Viral Oncology and Aging Research, The UCLA School of Dentistry.
The Shapiro Family Laboratory of Viral Oncology and Aging Research, The UCLA School of Dentistry; UCLA Jonsson Comprehensive Cancer Center.
J Vis Exp. 2017 Jan 12(119):54973. doi: 10.3791/54973.
Dental pulp is a vital organ of a tooth fully protected by enamel and dentin. When the pulp is exposed due to cariogenic or iatrogenic injuries, it is often capped with biocompatible materials in order to expedite pulpal wound healing. The ultimate goal is to regenerate reparative dentin, a physical barrier that functions as a "biological seal" and protects the underlying pulp tissue. Although this direct pulp-capping procedure has long been used in dentistry, the underlying molecular mechanism of pulpal wound healing and reparative dentin formation is still poorly understood. To induce reparative dentin, pulp capping has been performed experimentally in large animals, but less so in mice, presumably due to their small sizes and the ensuing technical difficulties. Here, we present a detailed, step-by-step method of performing a pulp-capping procedure in mice, including the preparation of a Class-I-like cavity, the placement of pulp-capping materials, and the restoration procedure using dental composite. Our pulp-capping mouse model will be instrumental in investigating the fundamental molecular mechanisms of pulpal wound healing in the context of reparative dentin in vivo by enabling the use of transgenic or knockout mice that are widely available in the research community.
牙髓是牙齿的重要器官,受到牙釉质和牙本质的充分保护。当牙髓因龋齿或医源性损伤而暴露时,通常会用生物相容性材料覆盖,以加速牙髓伤口愈合。最终目标是再生修复性牙本质,这是一种作为“生物密封”发挥作用并保护下方牙髓组织的物理屏障。尽管这种直接盖髓术在牙科领域长期使用,但牙髓伤口愈合和修复性牙本质形成的潜在分子机制仍知之甚少。为了诱导修复性牙本质形成,已在大型动物中进行了实验性盖髓,但在小鼠中较少进行,可能是由于其体型小以及随之而来的技术困难。在这里,我们展示了一种在小鼠中进行盖髓术的详细、分步方法,包括制备类I类洞、放置盖髓材料以及使用牙科复合材料的修复程序。我们的盖髓小鼠模型将有助于通过使用研究界广泛可用的转基因或基因敲除小鼠,在体内修复性牙本质的背景下研究牙髓伤口愈合的基本分子机制。