胞壁酰二肽对人牙髓细胞分化影响的研究  被引量:1

Effects of muramyl dipeptide on the differentiation of human dental pulp cells

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作  者:罗传霞[1] 张莉[1] 宋智[1] 秦伟[1] 林正梅[1] 

机构地区:[1]中山大学光华口腔医学院·附属口腔医院牙体牙髓病科·中山大学口腔医学研究所,广州510055

出  处:《中华口腔医学杂志》2011年第7期412-416,共5页Chinese Journal of Stomatology

基  金:国家自然科学基金(81070829)

摘  要:目的探讨天然免疫受体核苷酸结合寡聚化结构域蛋白2(nucleotide—binding oligomerization domain-2,NOD-2)在深龋牙髓组织中的表达及NOD-2特异性配体胞壁酰二肽(muramyl dipeptide,MDP)对人牙髓细胞分化的影响。方法实时荧光定量聚合酶链反应(PCR)法检测深龋及健康人牙髓组织中NOD-2表达差异;1mg/LMDP刺激体外培养的人牙髓细胞0、2、6、12、24h,实时荧光定量PCR、蛋白质免疫印迹法及免疫荧光检测NOD-2基因及蛋白表达;不同质量浓度MDP刺激人牙髓细胞24h,蛋白质免疫印迹法检测24h后牙本质涎蛋白(dentin sialoprotein,DSP)的表达;0.1mg/LMDP作用于人牙髓细胞0、2、6、12、24h,检测不同时间点牙本质涎磷蛋白(sialophosphoprotin,DSPP)、骨钙蛋白mRNA及骨桥蛋白的表达。结果深龋牙髓组织中NOD-2mRNA相对表达量为(0.2610±0.0824),较健康牙髓组织(0.0024±0.0002)显著增高(P〈0.05)。实时荧光定量PCR及蛋白质印迹法结果显示NOD-2表达随时间上调,免疫荧光检测证实NOD-2蛋白表达于胞质。MDP质量浓度为0.1mg/L时DSP蛋白表达量最大(0.3782±0.0564),并随MDP质量浓度增加而下降;DSPP、骨钙蛋白mRNA表达呈时间依赖性,12h达最大值,24h后有所下降;骨桥蛋白表达量随时间上调。结论深龋牙髓组织中NOD-2表达升高,MDP与人牙髓细胞的分化相关。Objective To investigate the nucleotide-binding oligomerization domain-2 (NOD-2) gene expression in deep caries and the effects of NOD-2 agonist muramyl dipeptide (MDP) on the differentiation of human dental pulp cells(hDPC). Methods NOD-2 gene level in deep caries and healthy pulp tissue was determined by real-time quantitative polymerase chain reaction (realtime-PCR). Reahime- PCR, Western blotting and immunofluoreseenee were performed to evaluate NOD-2 gene and protein expression. Dentin sialoprotein(DSP) protein level was assessed when hDPC were challenged by different concentrations of MDP for 24 hours, and sialophosphoprotein (DSPP) , osteocalcin (OCN) mRNA and osteopontin(OPN) protein level were detected at different time points after incubation with 0. 1 mg/L MDP. Results NOD-2 mRNA level was higher in pulp tissue of deep caries (0. 2610 ± 0. 0824 ) than that in healthy controls ( 0. 0024 ± 0. 0002 ) , P 〈 0.05. The expression of NOD-2 gene and protein increased in a time denpendent manner upon stimulation with MDP. Immunofluorescence confirmed that NOD-2 protein was located in cytoplasm. Moreover, 0. 1 mg/L MDP augmented DSP protein level. DSPP and OCN mRNA were elevated with time and reached the peak at 12 h and down-regulated. OPN protein level also increased with time. Conclusions Dental pulp NOD-2 expression are up-regulated in pulp tissue of deep caries. MDP may be related to the differentiation of hDPC.

关 键 词:Nod2信号接头蛋白质 乙酰胞壁酰-丙氨酸-异谷酰胺 细胞分化 牙髓细胞 

分 类 号:R781[医药卫生—口腔医学]

 

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