Stem cells are pluripotent cells, having a property of differentiating into various types of cells of human body. Several studies have developed mesenchymal stem cells(MSCs) from various human tissues,peripheral blood...Stem cells are pluripotent cells, having a property of differentiating into various types of cells of human body. Several studies have developed mesenchymal stem cells(MSCs) from various human tissues,peripheral blood and body fluids. These cells are then characterized by cellular and molecular markers to understand their specific phenotypes. Dental pulp stem cells(DPSCs) are having a MSCs phenotype and they are differentiated into neuron, cardiomyocytes, chondrocytes, osteoblasts, liver cells and β cells of islet of pancreas. Thus, DPSCs have shown great potentiality to use in regenerative medicine for treatment of various human diseases including dental related problems. These cells can also be developed into induced pluripotent stem cells by incorporation of pluripotency markers and use for regenerative therapies of various diseases. The DPSCs are derived from various dental tissues such as human exfoliated deciduous teeth, apical papilla, periodontal ligament and dental follicle tissue. This review will overview the information about isolation, cellular and molecular characterization and differentiation of DPSCs into various types of human cells and thus these cells have important applications in regenerative therapies for various diseases. This review will be most useful for postgraduate dental students as well as scientists working in the field of oral pathology and oral medicine.展开更多
目的:比较黏结剂S ingle bond 2不同涂布方式下牙本质黏结界面的形态学变化,为临床选择黏结剂应用方法提供参考依据。方法:暴露新鲜拔除的人第三磨牙牙本质,应用不同方式(包括涂布力度、方向、层数和固化次数)分组进行黏结剂涂布,然后,...目的:比较黏结剂S ingle bond 2不同涂布方式下牙本质黏结界面的形态学变化,为临床选择黏结剂应用方法提供参考依据。方法:暴露新鲜拔除的人第三磨牙牙本质,应用不同方式(包括涂布力度、方向、层数和固化次数)分组进行黏结剂涂布,然后,在环境扫描电镜下直接观察牙本质黏结界面的形态差异。根据黏结剂分布是否均匀、封闭牙本质小管的程度以及黏结剂渗入牙本质小管的情况判断效果。结果:黏结剂涂布力度方面,轻涂比重涂好;涂布方向,同向涂布比反复涂布好;涂布层数,涂2层较涂1层或4层好;固化方式,固化1次较固化2次好。结论:临床使用第五代黏结剂S ingle bond 2时,推荐同向轻涂2遍后固化的方法,可使黏结剂均匀分布,并较好地封闭牙本质小管。展开更多
目的:研究对比4种临床常用牙本质黏结剂的边缘封闭性。方法:12个离体前磨牙,在颊、舌侧牙颈部釉-牙骨质界处各制备直径2mm,深1.5mm盒型洞。随机分为4组,分别使用Single Bond、AdperPrompt、Clearfil SE Bond、Spread iBond黏结,3MZ250...目的:研究对比4种临床常用牙本质黏结剂的边缘封闭性。方法:12个离体前磨牙,在颊、舌侧牙颈部釉-牙骨质界处各制备直径2mm,深1.5mm盒型洞。随机分为4组,分别使用Single Bond、AdperPrompt、Clearfil SE Bond、Spread iBond黏结,3MZ250树脂充填。500g/L碱性硝酸银中浸泡24h,强光显影8h,沿牙体长轴通过充填体正中颊舌向纵行剖开,体视显微镜下观察各剖面充填体边缘的微渗漏情况,并以扫描电镜观察树脂-牙本质界面的结合状态。结果:各种黏结剂界面均存在微渗漏现象,实验组Single Bond、AdperPrompt、Clearfil SE Bond和Spread iBond渗漏深度分别为(777.23±120.13)μm、(930.12±130.10)μm、(240.33±120.53)μm、(640.12±170.23)μm。Clearfil SE Bond组银渗漏的深度明显低于其他组,(P<0.05),其他3组组间无显著性差异(P>0.05)。结论:临床上常用的4种黏结剂均不能避免牙本质黏结界面的渗漏,Clearfil SE Bond对牙本质的封闭性优于Adper Prompt、Spread iBond、Single Bond。展开更多
Phosphophoryn (PP) and dentin sialoprotein (DSP) are the most dominant non-collagenous proteins in dentin. PP is an extremely acidic protein that can function as a mineral nucleator for dentin mineralization. DSP was ...Phosphophoryn (PP) and dentin sialoprotein (DSP) are the most dominant non-collagenous proteins in dentin. PP is an extremely acidic protein that can function as a mineral nucleator for dentin mineralization. DSP was first identified in 1981, yet its functional significance is still controversial. Historically, these two proteins were considered to be independently synthesized and secreted by dental pulp cells into the developing dentin matrix. However, with the identification of the DSP coding sequence in 1994, followed2 years later by the finding that the PP coding sequence was located immediately downstream from the DSP sequence, it became immediately clear that DSP and PP proteins were derived from a single DSP-PP (i.e., dentin sialophosphoprotein, DSPP) transcript.Since DSPP cDNA became available, tremendous progress has been made in studying DSP-PP mRNA distribution and DSP generation from the DSP-PP precursor protein at specific cleavage sites by protease tolloid-related-1 (TLR1) or bone morphogenetic protein 1 (BMP1). The functions of DSP-PP and DSP were investigated via DSP-PP knockout (KO) and DSP knockin in DSP-PP KO mice. In addition, a number of in vitro studies aimed to elucidate DSPP and DSP function in dental pulp cells.展开更多
基金Supported by Jaslok Hospital and Research Centre,Mumbai,India,Project ni491,A/C 27814
文摘Stem cells are pluripotent cells, having a property of differentiating into various types of cells of human body. Several studies have developed mesenchymal stem cells(MSCs) from various human tissues,peripheral blood and body fluids. These cells are then characterized by cellular and molecular markers to understand their specific phenotypes. Dental pulp stem cells(DPSCs) are having a MSCs phenotype and they are differentiated into neuron, cardiomyocytes, chondrocytes, osteoblasts, liver cells and β cells of islet of pancreas. Thus, DPSCs have shown great potentiality to use in regenerative medicine for treatment of various human diseases including dental related problems. These cells can also be developed into induced pluripotent stem cells by incorporation of pluripotency markers and use for regenerative therapies of various diseases. The DPSCs are derived from various dental tissues such as human exfoliated deciduous teeth, apical papilla, periodontal ligament and dental follicle tissue. This review will overview the information about isolation, cellular and molecular characterization and differentiation of DPSCs into various types of human cells and thus these cells have important applications in regenerative therapies for various diseases. This review will be most useful for postgraduate dental students as well as scientists working in the field of oral pathology and oral medicine.
文摘目的:比较黏结剂S ingle bond 2不同涂布方式下牙本质黏结界面的形态学变化,为临床选择黏结剂应用方法提供参考依据。方法:暴露新鲜拔除的人第三磨牙牙本质,应用不同方式(包括涂布力度、方向、层数和固化次数)分组进行黏结剂涂布,然后,在环境扫描电镜下直接观察牙本质黏结界面的形态差异。根据黏结剂分布是否均匀、封闭牙本质小管的程度以及黏结剂渗入牙本质小管的情况判断效果。结果:黏结剂涂布力度方面,轻涂比重涂好;涂布方向,同向涂布比反复涂布好;涂布层数,涂2层较涂1层或4层好;固化方式,固化1次较固化2次好。结论:临床使用第五代黏结剂S ingle bond 2时,推荐同向轻涂2遍后固化的方法,可使黏结剂均匀分布,并较好地封闭牙本质小管。
文摘目的:研究对比4种临床常用牙本质黏结剂的边缘封闭性。方法:12个离体前磨牙,在颊、舌侧牙颈部釉-牙骨质界处各制备直径2mm,深1.5mm盒型洞。随机分为4组,分别使用Single Bond、AdperPrompt、Clearfil SE Bond、Spread iBond黏结,3MZ250树脂充填。500g/L碱性硝酸银中浸泡24h,强光显影8h,沿牙体长轴通过充填体正中颊舌向纵行剖开,体视显微镜下观察各剖面充填体边缘的微渗漏情况,并以扫描电镜观察树脂-牙本质界面的结合状态。结果:各种黏结剂界面均存在微渗漏现象,实验组Single Bond、AdperPrompt、Clearfil SE Bond和Spread iBond渗漏深度分别为(777.23±120.13)μm、(930.12±130.10)μm、(240.33±120.53)μm、(640.12±170.23)μm。Clearfil SE Bond组银渗漏的深度明显低于其他组,(P<0.05),其他3组组间无显著性差异(P>0.05)。结论:临床上常用的4种黏结剂均不能避免牙本质黏结界面的渗漏,Clearfil SE Bond对牙本质的封闭性优于Adper Prompt、Spread iBond、Single Bond。
文摘Phosphophoryn (PP) and dentin sialoprotein (DSP) are the most dominant non-collagenous proteins in dentin. PP is an extremely acidic protein that can function as a mineral nucleator for dentin mineralization. DSP was first identified in 1981, yet its functional significance is still controversial. Historically, these two proteins were considered to be independently synthesized and secreted by dental pulp cells into the developing dentin matrix. However, with the identification of the DSP coding sequence in 1994, followed2 years later by the finding that the PP coding sequence was located immediately downstream from the DSP sequence, it became immediately clear that DSP and PP proteins were derived from a single DSP-PP (i.e., dentin sialophosphoprotein, DSPP) transcript.Since DSPP cDNA became available, tremendous progress has been made in studying DSP-PP mRNA distribution and DSP generation from the DSP-PP precursor protein at specific cleavage sites by protease tolloid-related-1 (TLR1) or bone morphogenetic protein 1 (BMP1). The functions of DSP-PP and DSP were investigated via DSP-PP knockout (KO) and DSP knockin in DSP-PP KO mice. In addition, a number of in vitro studies aimed to elucidate DSPP and DSP function in dental pulp cells.
