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成釉细胞瘤和发育中的人类牙齿中的紧密连接蛋白1、4、5、7和闭合蛋白

Claudins 1, 4, 5, 7 and occludin in ameloblastomas and developing human teeth.

作者信息

Bello Ibrahim O, Soini Ylermi, Slootweg Pieter J, Salo Tuula

机构信息

Department of Diagnostics and Oral Medicine, Institute of Dentistry, University of Oulu, Oulu, Finland.

出版信息

J Oral Pathol Med. 2007 Jan;36(1):48-54. doi: 10.1111/j.1600-0714.2006.00497.x.

Abstract

BACKGROUND

To analyze the distribution pattern of claudins 1, 4, 5, 7 and occludin in benign and malignant ameloblastomas and developing human teeth.

METHODS

Paraffin-embedded tissue specimens of 25 benign and four malignant ameloblastomas and two developing human teeth were examined immunohistochemically using antibodies against claudins 1, 4, 5, 7 and occludin.

RESULTS

In ameloblastomas strongest expression was seen for claudins 1 and 7 while claudin 4 was expressed less frequently. Claudin 5 and occludin were seen only in a minority of cases. There were no evident differences in the expression of claudins or occludin neither between different histologic subtypes of ameloblastomas nor between benign or malignant cases. The strongest expression for claudins was present in the central stellatum reticulum-like cells surrounding the microcysts and in the areas with squamous differentiation of the ameloblastomas. In developing teeth both claudin 1 and 7 stained strongly in the enamel epithelium, ameloblasts, and enamel matrix, but staining for claudin 4 was relatively weak. Claudin 5 was preferentially expressed only in vessels, and occludin staining ranged from negative to weak in ameloblastomas and teeth germs.

CONCLUSION

There were no clear differences in the expression levels between benign and malignant ameloblastic tumors. The overexpression of claudins in the areas with microcyst formation may indicate their attempt to maintain the interepithelial cohesion of the cells. The strong immunoreactivity of ameloblasts and newly synthesized enamel matrix for claudins 1 and 7 indicates that they may be involved in cell signaling influencing enamel formation.

摘要

背景

分析闭合蛋白1、4、5、7及闭合小环蛋白在良性和恶性成釉细胞瘤以及发育中的人牙中的分布模式。

方法

采用抗闭合蛋白1、4、5、7及闭合小环蛋白的抗体,对25例良性和4例恶性成釉细胞瘤以及两颗发育中的人牙的石蜡包埋组织标本进行免疫组织化学检查。

结果

在成釉细胞瘤中,闭合蛋白1和7表达最强,而闭合蛋白4表达频率较低。闭合蛋白5和闭合小环蛋白仅在少数病例中可见。在成釉细胞瘤的不同组织学亚型之间以及良性或恶性病例之间,闭合蛋白或闭合小环蛋白的表达均无明显差异。闭合蛋白的最强表达出现在微囊肿周围的中央星网状样细胞以及成釉细胞瘤有鳞状分化的区域。在发育中的牙齿中,闭合蛋白1和7在釉质上皮、成釉细胞和釉质基质中均有强染色,但闭合蛋白4的染色相对较弱。闭合蛋白5仅在血管中优先表达,在成釉细胞瘤和牙胚中,闭合小环蛋白的染色从阴性到弱阳性不等。

结论

良性和恶性成釉细胞瘤性肿瘤的表达水平无明显差异。闭合蛋白在有微囊肿形成的区域过表达可能表明它们试图维持细胞间的上皮内聚力。成釉细胞和新合成的釉质基质对闭合蛋白1和7的强免疫反应性表明它们可能参与影响釉质形成的细胞信号传导。

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