Immunohistochemical analysis of heat-shock protein 27 in human tooth germ and ameloblastoma

Saikat Chakraborty, Ramesh Venkatapathy, B. Dhanasekaran, K. Prasad, Kashish Singh, S. Radhakrishnan
{"title":"Immunohistochemical analysis of heat-shock protein 27 in human tooth germ and ameloblastoma","authors":"Saikat Chakraborty, Ramesh Venkatapathy, B. Dhanasekaran, K. Prasad, Kashish Singh, S. Radhakrishnan","doi":"10.4103/ijofr.ijofr_7_18","DOIUrl":null,"url":null,"abstract":"Objective: The purpose of the study was to demonstrate the presence of heat-shock protein (HSP) 27 in developing tooth germs and ameloblastoma and compare their expressions. Materials and Methods: The study was conducted in the Department of Oral Pathology and Microbiology, Mahatma Gandhi Postgraduate Institute, Puducherry. Orofacial complexes of five abortus fetuses between 9th and 18th weeks were processed for fetal sections and ten formalin-fixed paraffin-embedded tissues for ameloblastoma were taken up from the archives of the department. All tissues were stained for routine hematoxylin and eosin, and immunohistochemistry was done using anti-HSP27 antibody. Results: Dental lamina was found positive for HSP27 in all the five cases; succedaneous bud stage was found positive in two of five cases. Stellate reticulum and outer enamel epithelium were found positive in one each of five cases and inner enamel epithelium was negative in all five cases. In ameloblastoma, ten cases were studied in which positivity was seen in the columnar or cuboidal cells of the tumor islands in various histological variants of ameloblastoma. Conclusion: The immunostaining pattern of HSP27 revealed that the differentiation level of ameloblastoma corresponds to the differentiation level of odontogenic cells in tooth germ and that HSP27 might play a role in this. Further, HSP27 can be taken up as a marker of differentiation of ameloblasts along with markers such as cytokeratin 19.","PeriodicalId":245370,"journal":{"name":"International Journal of Orofacial Research","volume":"3 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Orofacial Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ijofr.ijofr_7_18","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: The purpose of the study was to demonstrate the presence of heat-shock protein (HSP) 27 in developing tooth germs and ameloblastoma and compare their expressions. Materials and Methods: The study was conducted in the Department of Oral Pathology and Microbiology, Mahatma Gandhi Postgraduate Institute, Puducherry. Orofacial complexes of five abortus fetuses between 9th and 18th weeks were processed for fetal sections and ten formalin-fixed paraffin-embedded tissues for ameloblastoma were taken up from the archives of the department. All tissues were stained for routine hematoxylin and eosin, and immunohistochemistry was done using anti-HSP27 antibody. Results: Dental lamina was found positive for HSP27 in all the five cases; succedaneous bud stage was found positive in two of five cases. Stellate reticulum and outer enamel epithelium were found positive in one each of five cases and inner enamel epithelium was negative in all five cases. In ameloblastoma, ten cases were studied in which positivity was seen in the columnar or cuboidal cells of the tumor islands in various histological variants of ameloblastoma. Conclusion: The immunostaining pattern of HSP27 revealed that the differentiation level of ameloblastoma corresponds to the differentiation level of odontogenic cells in tooth germ and that HSP27 might play a role in this. Further, HSP27 can be taken up as a marker of differentiation of ameloblasts along with markers such as cytokeratin 19.
人牙胚和成釉细胞瘤热休克蛋白27的免疫组化分析
目的:研究热休克蛋白(HSP) 27在牙胚和成釉细胞瘤发育过程中的表达,并比较其表达。材料与方法:本研究在印度普杜切里圣雄甘地研究生院口腔病理与微生物学系进行。对5例9 ~ 18周流产胎儿的口面部复合体进行胎儿切片处理,并从科档案中提取10例福尔马林固定石蜡包埋成釉细胞瘤组织。所有组织进行常规苏木精和伊红染色,并用抗hsp27抗体进行免疫组化。结果:5例患者牙板HSP27均阳性;5例中2例继发芽期阳性。星状网和外釉质上皮均为阳性,内釉质上皮均为阴性。在成釉细胞瘤中,我们研究了10例不同组织学变异的成釉细胞瘤的肿瘤岛柱状或立方细胞阳性。结论:HSP27的免疫染色显示成釉细胞瘤的分化水平与牙胚中牙源性细胞的分化水平相对应,HSP27可能与此有关。此外,HSP27可以与细胞角蛋白19等标记物一起作为成釉细胞分化的标记物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信