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关节盘内紊乱的颞下颌关节盘 MMP-7 和 MMP-9 的免疫组织化学定位的离体研究。

An ex vivo study on immunohistochemical localization of MMP-7 and MMP-9 in temporomandibular joint discs with internal derangement.

机构信息

Department of Bio-Medical Sciences, Anatomy Section, University of Catania, 95123 Catania, Italy.

出版信息

Eur J Histochem. 2013 Apr 15;57(2):e12. doi: 10.4081/ejh.2013.e12.

DOI:10.4081/ejh.2013.e12
PMID:23807291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3794338/
Abstract

Internal derangement (ID) is among the most common disorders of the temporomandibular joint (TMJ). Previous research by our group highlighted a correlation between apoptosis and TMJ ID. Metalloproteinases (MMP)-7 and -9 have been shown to play an important role in extracellular matrix ECM) homeostasis and, through it, in joint disc remodelling. The immunohistochemical expression of MMP-7 and -9 was investigated in discs from patients with TMJ ID and from healthy donors and compared with the degree of histological tissue degeneration. The collagen fibre arrangement in pathological discs exhibited varying degrees of disruption. New vessels were consistently detected; endothelial cells from these vessels were immunolabelled with both MMP-7 and MMP-9. More or less intense MMP-7 and MMP-9 immunolabelling was detected in the cytoplasm of disc cells from all patients. MMP-7 and MMP-9 immunostaining was significantly different between pathological and normal discs and correlated with the extent of histopathological degeneration. MMP-7 and MMP-9 upregulation in discs from patients with TMJ ID demonstrates their involvement in disc damage in this disorder. A greater understanding of these processes could help identify ways to curb MMP overproduction without affecting their tissue remodelling action. The design of specific inhibitors for these MMPs would not only help to gain insights into the biological roles of MMPs, but would also aid in developing therapeutic interventions for diseases associated with abnormal ECM degradation.

摘要

关节内紊乱(ID)是颞下颌关节(TMJ)最常见的疾病之一。我们小组之前的研究强调了细胞凋亡与 TMJ ID 之间的相关性。金属蛋白酶(MMP)-7 和 -9 已被证明在细胞外基质(ECM)稳态中发挥重要作用,并通过其在关节盘重塑中发挥作用。研究了 MMP-7 和 -9 在 TMJ ID 患者和健康供体的关节盘中的免疫组织化学表达,并与组织退变的程度进行了比较。病理性关节盘中的胶原纤维排列表现出不同程度的破坏。始终检测到新血管;这些血管的内皮细胞用 MMP-7 和 MMP-9 进行免疫标记。所有患者的盘细胞胞质中均检测到或多或少强烈的 MMP-7 和 MMP-9 免疫染色。病理性和正常关节盘之间的 MMP-7 和 MMP-9 免疫染色有显著差异,并与组织病理学退变的程度相关。TMJ ID 患者关节盘中 MMP-7 和 MMP-9 的上调表明它们参与了该疾病中盘损伤的发生。更深入地了解这些过程可以帮助确定在不影响其组织重塑作用的情况下抑制 MMP 过度产生的方法。这些 MMP 的特异性抑制剂的设计不仅有助于深入了解 MMP 的生物学作用,还有助于开发与异常 ECM 降解相关疾病的治疗干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/3794338/fe0bd514f80e/ejh-2013-2-e12-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/3794338/3e59d3a20eab/ejh-2013-2-e12-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/3794338/48e70f74cfdc/ejh-2013-2-e12-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/3794338/fe0bd514f80e/ejh-2013-2-e12-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/3794338/3e59d3a20eab/ejh-2013-2-e12-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/3794338/48e70f74cfdc/ejh-2013-2-e12-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/3794338/fe0bd514f80e/ejh-2013-2-e12-g003.jpg

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