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Notch-2在大鼠牙髓炎中的时空分布及其意义 被引量:3

Time-sequenced alteration of immunolocalization and significance of Notch-2 expression in rat pulpitis
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摘要 目的:研究单纯开髓导致大鼠牙髓炎进程中Notch-2在牙髓损伤修复中的作用。方法:通过开髓建立大鼠牙髓炎模型,用免疫组织化学染色方法研究Notch-2的时空表达变化及其意义。结果:牙髓损伤早期(3 d),牙髓间充质细胞和牙髓成纤维细胞中Notch-2均呈弱阳性表达,成牙本质细胞为阴性表达。牙髓损伤中期(5 d),靠近损伤区的成牙本质细胞深层细胞Notch-2阳性表达达到高峰;同时,新生毛细血管内皮细胞呈强阳性表达。牙髓损伤晚期(7 d),Notch-2在牙髓间充质细胞、血管内皮细胞中表达均减弱,而在成牙本质细胞阳性表达达到高峰。牙髓损伤末期(14 d),Notch-2仅在成牙本质细胞下层细胞中尚有微弱表达,而其余牙髓细胞均为阴性表达。对照组正常牙髓组织Notch-2表达为阴性。结论:Notch-2在牙髓损伤应激情况下在牙髓间充质细胞和成牙本质细胞中上调表达,对于启动牙髓自我修复、诱导牙髓间充质细胞功能性分化以及抑制受损成牙本质细胞凋亡、维系和调动其相对正常的生理功能可能具有重要作用。 Objective: To investigate the immunolocalization and significance of Notch-2 expression in the process of dental pulp repair after injury. Methods: An experimental animal model of injury-induced pulpitis was established to observe the time-sequenced alteration of the expression of Notch-2. Results: Three clays post-operation, weak positive staining of Notch-2 was observed in pulp mesenchyme ceils and pulp fibroblasts but not in vascular endothelial cells or odontoblasts. Five days post-operation, strong Notch-2 reactivity was found in subodontoblasts as well as newly born capillary endothelial cells. Seven days after cavity preparation, Notch-2 staining became weaker in pulp mesenchyme cells and capillary endothelial cells, but stronger positive staining was found in odontoblasts. Two weeks post-operation, weak Notch-2 staining was seen in pulp mesenchyme cells and subodontoblasfic layer cells and was absent from odontoblasts. Notch-2 immunoreactivity was completely absent in intact rat dental pulp. Conclusion: Notch-2 is strikingly up-regulated in dental pulp mesenchyme cells in the early clays after dental injury and then shows progressively up-regulation in odontoblasts. Properly regulated activation of Notch signaling pathway is important for controlling cell fate and maintaining the correct balance among cell proliferation, differentiation and apoptosis during dental pulp repair process.
出处 《实用口腔医学杂志》 CAS CSCD 北大核心 2009年第6期798-802,共5页 Journal of Practical Stomatology
基金 国家自然科学基金资助项目(编号:30600708) 教育部留学回国启动基金(编号:HG3103)
关键词 Notch-2 牙齿 成牙本质细胞 损伤修复 Notch-2 Tooth Odontoblasts Wound healing
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参考文献15

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同被引文献31

  • 1郭卫拉,赵守亮,周黎安,藏晓霞.Notch1信号蛋白在早期牙髓损伤修复中表达的免疫组化研究[J].临床口腔医学杂志,2005,21(3):156-157. 被引量:1
  • 2朱奇,樊明文,张旗,陈智,边专.转化生长因子β1(TGF-β1)和骨形成蛋白2(BMP2)体外联合诱导成牙本质细胞样细胞分化[J].口腔医学研究,2005,21(4):357-360. 被引量:2
  • 3Artavanis-Tsakonas S, Rand MD, Lake RJ. Notch signaling: cell fate control and signal integration in development [J]. Science, 1999, 284(5415)∶770-776.
  • 4Cai X, Gong P, Huang Y, et al. Notch signalling pathway in tooth development and adult dental cells [J]. Cell Prolif, 2011, 44(6)∶495-507.
  • 5Mitsiadis T A, Fried K, Goridis C. Reactivation of Delta-Notch signaling after injury: complementary expression patterns of ligand and receptor in dental pulp [J]. Exp Cell Res, 1999, 246(2)∶312-318.
  • 6Mitsiadis T A, Romeas A, Lendahl U, et al. Notch2 protein distribution in human teeth under normal and pathological conditions [J]. Exp Cell Res, 2003, 282(1)∶101-109.
  • 7Mitsiadis T A, De Bari C, About I. Apoptosis in developmental and repair-related human tooth remodeling: a view from the inside [J]. Exp Cell Res, 2008, 314(4)∶869-877.
  • 8Kim JY, Cha YG, Cho SW, et al. Inhibition of apoptosis in early tooth development alters tooth shape and size [J]. J Dent Res, 2006, 85(6)∶530-535.
  • 9Mitsiadis TA, Rahiotis C. Parallels between tooth development and repair: conserved molecular mechanisms following carious and dental injury [J]. J Dent Res, 2004,83(12)∶896-902.
  • 10Morse DR. Age-related changes of the dental pulp complex and their relationship to systemic aging [J]. Oral Surg Oral Med Oral Pathol, 1991, 72(6)∶721-745.

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