• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

金属蛋白酶与其组织抑制剂之间的失衡参与疱疹样皮炎的发病机制。

The imbalance between metalloproteinases and their tissue inhibitors is involved in the pathogenesis of dermatitis herpetiformis.

作者信息

Zebrowska Agnieszka, Narbutt Joanna, Sysa-Jedrzejowska Anna, Kobos Jozef, Waszczykowska Elzbieta

机构信息

Department of Dermatology and Venereology, Medical University of Lodz, Poland.

出版信息

Mediators Inflamm. 2005 Dec 14;2005(6):373-9. doi: 10.1155/MI.2005.373.

DOI:10.1155/MI.2005.373
PMID:16489258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1533900/
Abstract

Dermatitis herpetiformis (DH) is a subepidermal autoimmune disease characterized by skin and intestinal lesions consistent with coeliac disease. There are also some data that metalloproteinases (MMPs) are involved in the development of skin lesions in DH, however their exact role in this process is not fully understood. The aim of the study was to investigate whether MMPs and their inhibitors are involved in pathogenesis of DH. Skin biopsies were taken from 13 patients with active DH and from 10 healthy subjects. The localization and expression of MMPs and TIMPs were examined by immunohistochemistry. MMPs expression was detected in basal keratinocytes and in the whole epidermis in all of the DH subjects. Neutrophils in microabscesses and in blister fluid were also positive for MMPs. Expression of TIMPs was moderate or weak in all examined biopsies. Our results allow us to conclude that imbalance between these enzymes takes an important role in the pathogenesis of DH.

摘要

疱疹样皮炎(DH)是一种表皮下自身免疫性疾病,其特征为皮肤和肠道病变,与乳糜泻相符。也有一些数据表明金属蛋白酶(MMPs)参与了DH皮肤病变的发展,然而它们在这个过程中的确切作用尚未完全明确。本研究的目的是调查MMPs及其抑制剂是否参与DH的发病机制。从13例活动期DH患者和10名健康受试者身上获取皮肤活检样本。通过免疫组织化学检查MMPs和组织金属蛋白酶抑制剂(TIMPs)的定位和表达。在所有DH受试者中,MMPs在基底角质形成细胞和整个表皮中均有表达。微脓肿和水疱液中的中性粒细胞MMPs也呈阳性。在所有检查的活检样本中,TIMPs的表达为中度或弱阳性。我们的结果使我们得出结论,这些酶之间的失衡在DH的发病机制中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fe2/1533900/9dfd11134ef3/MI2005-373.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fe2/1533900/71528e874e6b/MI2005-373.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fe2/1533900/dbbae08580ec/MI2005-373.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fe2/1533900/5bc71c919261/MI2005-373.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fe2/1533900/992c0412e388/MI2005-373.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fe2/1533900/9dfd11134ef3/MI2005-373.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fe2/1533900/71528e874e6b/MI2005-373.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fe2/1533900/dbbae08580ec/MI2005-373.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fe2/1533900/5bc71c919261/MI2005-373.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fe2/1533900/992c0412e388/MI2005-373.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fe2/1533900/9dfd11134ef3/MI2005-373.005.jpg

相似文献

1
The imbalance between metalloproteinases and their tissue inhibitors is involved in the pathogenesis of dermatitis herpetiformis.金属蛋白酶与其组织抑制剂之间的失衡参与疱疹样皮炎的发病机制。
Mediators Inflamm. 2005 Dec 14;2005(6):373-9. doi: 10.1155/MI.2005.373.
2
Disturbances of the expression of metalloproteinases and their tissue inhibitors cause destruction of the basement membrane in pemphigoid.金属蛋白酶及其组织抑制剂表达的紊乱导致类天疱疮中基底膜的破坏。
Pol J Pathol. 2006;57(2):71-6.
3
Expression of matrix metalloproteinases and their endogenous tissue inhibitors in skin lesions from patients with tuberous sclerosis.结节性硬化症患者皮肤病变中基质金属蛋白酶及其内源性组织抑制剂的表达
J Am Acad Dermatol. 2004 Oct;51(4):526-33. doi: 10.1016/j.jaad.2004.01.055.
4
Relationship between matrix metalloproteinases/tissue inhibitors of matrix metalloproteinases systems and autoantibody patterns in systemic sclerosis.基质金属蛋白酶/基质金属蛋白酶组织抑制剂系统与系统性硬化症自身抗体模式之间的关系
Clin Biochem. 2007 Aug;40(12):837-42. doi: 10.1016/j.clinbiochem.2007.03.023. Epub 2007 Apr 19.
5
Collagen and elastin degradation by matrix metalloproteinases and tissue inhibitors of matrix metalloproteinase in aortic dissection.基质金属蛋白酶和基质金属蛋白酶组织抑制剂在主动脉夹层中对胶原蛋白和弹性蛋白的降解作用
Hum Pathol. 2000 Jun;31(6):640-6. doi: 10.1053/hupa.2000.7642.
6
Altered matrix metalloproteinases and tissue inhibitors of metalloproteinases in embryos from diabetic rats during early organogenesis.早期器官发生期糖尿病大鼠胚胎中基质金属蛋白酶和金属蛋白酶组织抑制剂的改变。
Reprod Toxicol. 2011 Dec;32(4):449-62. doi: 10.1016/j.reprotox.2011.09.003. Epub 2011 Sep 24.
7
Increased expression of matrix metalloproteinase-2, matrix metalloproteinase-9 and matrix metalloproteinase-13 in lesional skin of bullous pemphigoid.大疱性类天疱疮皮损中基质金属蛋白酶-2、基质金属蛋白酶-9和基质金属蛋白酶-13的表达增加。
Int Arch Allergy Immunol. 2006;139(2):104-13. doi: 10.1159/000090385. Epub 2005 Dec 19.
8
Expression of matrix metalloproteinases and their inhibitors in experimental retinal ischemia-reperfusion injury in rats.基质金属蛋白酶及其抑制剂在大鼠实验性视网膜缺血再灌注损伤中的表达
Exp Eye Res. 2002 May;74(5):577-84. doi: 10.1006/exer.2001.1152.
9
In situ gene expression and localization of metalloproteinases MMP1, MMP2, MMP3, MMP9, and their inhibitors TIMP1 and TIMP2 in human renal cell carcinoma.金属蛋白酶MMP1、MMP2、MMP3、MMP9及其抑制剂TIMP1和TIMP2在人肾细胞癌中的原位基因表达及定位
Oncol Rep. 2006 May;15(5):1379-84.
10
Expression of matrix metalloproiteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) in hepatocellular carcinoma tissue, compared with the surrounding non-tumor tissue.与周围非肿瘤组织相比,基质金属蛋白酶(MMPs)和金属蛋白酶组织抑制剂(TIMPs)在肝细胞癌组织中的表达情况。
Res Commun Mol Pathol Pharmacol. 2004;115-116:143-50.

引用本文的文献

1
Etiopathogenesis of dermatitis herpetiformis.疱疹样皮炎的病因发病机制。
Postepy Dermatol Alergol. 2022 Feb;39(1):1-6. doi: 10.5114/ada.2020.101637. Epub 2022 Feb 28.
2
Influence of lymphatic endothelial cells on proliferation and invasiveness of esophageal carcinoma cells in vitro and lymphangiogenesis in vivo.淋巴管内皮细胞对食管癌细胞体外增殖和侵袭能力及体内淋巴管生成的影响。
Med Oncol. 2015 Aug;32(8):222. doi: 10.1007/s12032-015-0662-3. Epub 2015 Jul 23.
3
Gene expression profiling in dermatitis herpetiformis skin lesions.

本文引用的文献

1
Epidermal transglutaminase (TGase 3) is the autoantigen of dermatitis herpetiformis.表皮转谷氨酰胺酶(TGase 3)是疱疹样皮炎的自身抗原。
J Exp Med. 2002 Mar 18;195(6):747-57. doi: 10.1084/jem.20011299.
2
Dermatitis herpetiformis.疱疹样皮炎
Clin Dermatol. 2001 Nov-Dec;19(6):728-36. doi: 10.1016/s0738-081x(00)00184-x.
3
Parallel expression of macrophage metalloelastase (MMP-12) in duodenal and skin lesions of patients with dermatitis herpetiformis.巨噬细胞金属弹性蛋白酶(MMP - 12)在疱疹样皮炎患者十二指肠和皮肤病变中的平行表达。
疱疹样皮炎皮肤病变中的基因表达谱分析。
Clin Dev Immunol. 2012;2012:198956. doi: 10.1155/2012/198956. Epub 2012 Sep 6.
4
Role of intestinal bacteria in gliadin-induced changes in intestinal mucosa: study in germ-free rats.肠内细菌在麦胶蛋白诱导的肠黏膜变化中的作用:无菌大鼠的研究。
PLoS One. 2011 Jan 13;6(1):e16169. doi: 10.1371/journal.pone.0016169.
5
[Dermatitis herpetiformis. An update of the pathogenesis].[疱疹样皮炎。发病机制的最新进展]
Hautarzt. 2009 Aug;60(8):627-30, 632. doi: 10.1007/s00105-008-1679-8.
Gut. 2001 Apr;48(4):496-502. doi: 10.1136/gut.48.4.496.
4
Matrix metalloproteinases.基质金属蛋白酶
J Biol Chem. 1999 Jul 30;274(31):21491-4. doi: 10.1074/jbc.274.31.21491.
5
Gelatinases in drug-induced toxic epidermal necrolysis.药物性中毒性表皮坏死松解症中的明胶酶
Eur J Clin Invest. 1998 Jul;28(7):528-32. doi: 10.1046/j.1365-2362.1998.00329.x.
6
Gelatinase B-deficient mice are resistant to experimental bullous pemphigoid.明胶酶B缺陷小鼠对实验性大疱性类天疱疮具有抗性。
J Exp Med. 1998 Aug 3;188(3):475-82. doi: 10.1084/jem.188.3.475.
7
Th2-like cytokine activity in dermatitis herpetiformis.疱疹样皮炎中的Th2样细胞因子活性。
Br J Dermatol. 1998 Feb;138(2):242-7. doi: 10.1046/j.1365-2133.1998.02068.x.
8
Identification of tissue transglutaminase as the autoantigen of celiac disease.鉴定组织转谷氨酰胺酶为乳糜泻的自身抗原。
Nat Med. 1997 Jul;3(7):797-801. doi: 10.1038/nm0797-797.
9
Urokinase plasminogen activator is expressed by basal keratinocytes before interstitial collagenase, stromelysin-1, and laminin-5 in experimentally induced dermatitis herpetiformis lesions.在实验性诱导的疱疹样皮炎病变中,尿激酶型纤溶酶原激活剂在基底角质形成细胞中比间质胶原酶、基质溶解素-1和层粘连蛋白-5更早表达。
J Invest Dermatol. 1997 Jan;108(1):7-11. doi: 10.1111/1523-1747.ep12285610.
10
Deposition of granular IgA relative to clinical lesions in dermatitis herpetiformis.疱疹样皮炎中颗粒状IgA相对于临床皮损的沉积情况。
Arch Dermatol. 1996 Aug;132(8):912-8.