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糖尿病性和非糖尿病性炎症牙龈中角质形成细胞增殖的比较。

Comparison of keratinocyte proliferation in diabetic and non-diabetic inflamed gingiva.

作者信息

Açikgoz Gökhan, Devrim Inci, Ozdamar Sükrü

机构信息

University of Ondokuz Mayis, Faculty of Dentistry, Department of Periodontology, Samsun, Turkey.

出版信息

J Periodontol. 2004 Jul;75(7):989-94. doi: 10.1902/jop.2004.75.7.989.

Abstract

BACKGROUND

Keratinocytes are chiefly cells of the epidermis but also constitute 90% of the gingival cells. The molecular mechanisms of proliferative activity in keratinization whereby diabetes alters periodontal physiology have not been elucidated. In this study, we aimed to investigate the role of gingival keratinocytes in hyperglycemic subjects by examining their mitotic activities.

METHODS

We tested 30 patients with periodontitis, of whom 15 were type II diabetics and the remainder systemically healthy. Biopsies were obtained from the bottom of the deepest pocket in each subject by reverse beveled incision. Formalin-fixed and paraffin-embedded specimens were then processed for periodic acid-Schiff (PAS)-diastase histochemistry and proliferating cell nuclear antigen (PCNA) (P10). Immunohistochemical studies were employed to determine the presence of PCNA and were used to detect the proliferating potential of keratinocytes needed in synthesizing DNA. The expression of PCNA was evaluated using an immunoperoxidase technique and PC10 monoclonal antibody to PCNA. Mitotic index was calculated from basal cells. Statistical analysis employed the chi-square test.

RESULTS

No significant difference between the diabetic and non-diabetic patients was found in the mitotic index of the oral-gingival epithelium.

CONCLUSION

Although the mitotic index in patients with diabetes was slightly lower, keratinization in the gingival tissues for both groups was essentially identical.

摘要

背景

角质形成细胞主要是表皮细胞,但也构成牙龈细胞的90%。糖尿病改变牙周生理的角质化过程中增殖活性的分子机制尚未阐明。在本研究中,我们旨在通过检查牙龈角质形成细胞的有丝分裂活性来研究其在高血糖受试者中的作用。

方法

我们测试了30例牙周炎患者,其中15例为II型糖尿病患者,其余患者全身健康。通过反向斜面切口从每个受试者最深牙周袋底部获取活检组织。然后将福尔马林固定、石蜡包埋的标本进行过碘酸希夫(PAS)-淀粉酶组织化学和增殖细胞核抗原(PCNA)(P10)处理。采用免疫组织化学研究来确定PCNA的存在,并用于检测合成DNA所需的角质形成细胞的增殖潜力。使用免疫过氧化物酶技术和PC10抗PCNA单克隆抗体评估PCNA的表达。从基底细胞计算有丝分裂指数。统计分析采用卡方检验。

结果

糖尿病患者和非糖尿病患者口腔牙龈上皮的有丝分裂指数无显著差异。

结论

虽然糖尿病患者的有丝分裂指数略低,但两组牙龈组织的角质化基本相同。

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