Department of Oral and Maxillofacial Surgery, Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
PLoS One. 2013 May 10;8(5):e62645. doi: 10.1371/journal.pone.0062645. Print 2013.
The aim of the present study was to investigate the effect of Sonic hedgehog (Shh) on human dental pulp cells (hDPCs) and the potential of complexes with Shh gene modified hDPCs and porous calcium phosphate cement (CPC) for mineralized tissue formation. hDPCs were cultured and transfected with adenoviral mediated human Shh gene (AdShh). Overexpression of Shh and cell proliferation was tested by real-time PCR analysis, western blotting analysis, and MTT analysis, respectively. The odontoblastic differentiation was assessed by alkaline phosphatase (ALP) activity and real-time PCR analysis on markers of Patched-1 (Ptc-1), Smoothened (Smo), Gli 1, Gli 2, Gli 3, osteocalcin (OCN), dentin matrix protein-1 (DMP-1), and dentin sialophosphoprotein (DSPP). Finally, AdShh-transfected hDPCs were combined with porous CPC and placed subcutaneously in nude mice for 8 and 12 weeks, while AdEGFP-transfected and untransfected hDPCs were treated as control groups. Results indicated that Shh could promote proliferation and odontoblastic differentiation of hDPCs, while Shh/Gli 1 signaling pathway played a key role in this process. Importantly, more mineralized tissue formation was observed in combination with AdShh transfected hDPCs and porous CPC, moreover, the mineralized tissue exhibited dentin-like features such as structures similar to dentin-pulp complex and the positive staining for DSPP protein similar to the tooth tissue. These results suggested that the constructs with AdShh-transfected hDPCs and porous CPC might be a better alternative for dental tissue regeneration.
本研究旨在探讨 Sonic hedgehog (Shh) 对人牙髓细胞 (hDPCs) 的影响,以及 Shh 基因修饰的 hDPCs 与多孔磷酸钙水泥 (CPC) 复合物在矿化组织形成中的潜力。hDPCs 经腺病毒介导的人 Shh 基因 (AdShh) 转染后进行培养。通过实时 PCR 分析、western blot 分析和 MTT 分析分别检测 Shh 的过表达和细胞增殖情况。碱性磷酸酶 (ALP) 活性和实时 PCR 分析用于评估牙本质细胞分化的标志物,包括 Patched-1 (Ptc-1)、Smoothened (Smo)、Gli 1、Gli 2、Gli 3、骨钙素 (OCN)、牙本质基质蛋白-1 (DMP-1) 和牙本质涎磷蛋白 (DSPP)。最后,将 AdShh 转染的 hDPCs 与多孔 CPC 结合后,皮下植入裸鼠体内 8 周和 12 周,同时将 AdEGFP 转染和未转染的 hDPCs 作为对照组。结果表明,Shh 可促进 hDPCs 的增殖和牙本质细胞分化,而 Shh/Gli 1 信号通路在这一过程中起着关键作用。重要的是,与 AdShh 转染的 hDPCs 和多孔 CPC 结合后,观察到更多的矿化组织形成,并且矿化组织表现出类似于牙髓复合体的结构和类似于牙组织的 DSPP 蛋白阳性染色的牙本质样特征。这些结果表明,含有 AdShh 转染的 hDPCs 和多孔 CPC 的构建物可能是牙组织再生的更好选择。