Nayak Aarati, Raikar Anita, Kotrashetti Vijaylaxmi, Nayak Ramakant, Shree Sumedha, Kambali Soumya
Department of Periodontology, Maratha Mandal's NGH Institute of Dental Science and Research Centre, Belgaum, Karnataka, India.
Department of Oral Pathology and Microbiology, Maratha Mandal's NGH Institute of Dental Science and Research Centre, Belgaum, Karnataka, India.
J Indian Soc Periodontol. 2016 May-Jun;20(3):294-8. doi: 10.4103/0972-124X.182601.
Apoptosis plays a critical role in the regulation of inflammation and host immune response. It helps in tissue homeostasis and a disturbance in this is often associated with disease. The use of histochemical stains like hematoxylin and eosin (H and E) and methyl green-pyronin (MGP) can provide a simple and cost-effective method for the detection of apoptotic cells.
Study intended to analyze the expression of apoptosis in the gingival epithelium of healthy subjects and in patients with chronic periodontitis, using H and E and MGP. It is also proposed to correlate the apoptotic index (AI) of healthy individuals and those with chronic periodontitis.
Twenty gingival biopsies were harvested from which ten samples were of healthy subjects and ten subjects who suffered from chronic periodontitis. Apoptotic cells were analyzed using MGP and H and E under light microscopy.
Apoptotic cells were identified at ×100 magnification and AI was calculated. Apoptotic cells were easily distinguishable in MGP stained sections when compared to those stained using H and E. Moreover, apoptotic cell count was higher in chronic periodontitis. Statistical analyses were done by Tukey's multiple post hoc procedure.
The study reveals that MGP staining can be used in a routine basic laboratory set up as one of the cost-effective methods for the detection of apoptotic cells.
细胞凋亡在炎症调节和宿主免疫反应中起关键作用。它有助于维持组织稳态,而这种稳态的紊乱通常与疾病相关。使用苏木精和伊红(H&E)以及甲基绿-派洛宁(MGP)等组织化学染色方法可为检测凋亡细胞提供一种简单且经济高效的方法。
本研究旨在使用H&E和MGP分析健康受试者和慢性牙周炎患者牙龈上皮中细胞凋亡的表达情况。还拟对健康个体和慢性牙周炎患者的凋亡指数(AI)进行相关性分析。
采集20份牙龈活检样本,其中10份来自健康受试者,10份来自慢性牙周炎患者。在光学显微镜下使用MGP以及H&E对凋亡细胞进行分析。
在100倍放大倍数下识别凋亡细胞并计算AI。与使用H&E染色的切片相比,在MGP染色的切片中凋亡细胞更容易辨别。此外,慢性牙周炎患者的凋亡细胞计数更高。采用Tukey多重事后检验程序进行统计分析。
该研究表明,MGP染色可作为一种经济高效的凋亡细胞检测方法用于常规基础实验室。