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人龋损牙本质中的细胞凋亡激活:一项免疫组织化学研究。

Apoptosis activation in human carious dentin. An immunohistochemical study.

作者信息

Loreto C, Psaila A, Musumeci G, Castorina S, Leonardi R

机构信息

University of Catania.

出版信息

Eur J Histochem. 2015 Jul 9;59(3):2513. doi: 10.4081/ejh.2015.2513.

Abstract

The exact mechanisms and enzymes involved in caries progression are largely unclear. Apoptosis plays a key role in dentin remodelling related to damage repair; however, it is unclear whether apoptosis in decayed teeth is activated through the extrinsic or the intrinsic pathway. This ex vivo immunohistochemical study explored the localization of TRAIL, DR5, Bcl-2 and Bax, the main proteins involved in apoptosis, in teeth with advanced caries. To evaluate TRAIL, DR5, Bcl-2 and Bax immunoexpressions twelve permanent carious premolars were embedded in paraffin and processed for immunohistochemistry. The results showed that TRAIL and DR5 were overexpressed in dentin and in pulp vessels and mononuclear cells; strong Bax immunostaining was detected in dilated dentinal tubules close to the lesion, and Bcl-2 staining was weak in some dentin areas under the cavity or altogether absent. These findings suggest that both apoptosis pathways are activated in dental caries. Further studies are required to gain insights into its biomolecular mechanisms.

摘要

龋齿进展的确切机制和相关酶类在很大程度上尚不清楚。细胞凋亡在与损伤修复相关的牙本质重塑中起关键作用;然而,尚不清楚龋坏牙齿中的细胞凋亡是通过外源性途径还是内源性途径激活的。这项体外免疫组织化学研究探讨了参与细胞凋亡的主要蛋白质TRAIL、DR5、Bcl-2和Bax在晚期龋齿牙齿中的定位。为了评估TRAIL、DR5、Bcl-2和Bax的免疫表达,将12颗恒龋前磨牙嵌入石蜡中并进行免疫组织化学处理。结果显示,TRAIL和DR5在牙本质、牙髓血管和单核细胞中过度表达;在靠近病变的扩张牙本质小管中检测到强烈的Bax免疫染色,而在龋洞下方的一些牙本质区域Bcl-2染色较弱或完全缺失。这些发现表明,在龋齿中两种细胞凋亡途径均被激活。需要进一步研究以深入了解其生物分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497c/4598594/a1e901e2ce33/ejh-2015-3-2513-g001.jpg

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