组织蛋白酶:腹主动脉瘤背后的新罪魁祸首。

IF 2 Regenerative Medicine Research Pub Date : 2013-11-01 eCollection Date: 2013-12-01 DOI:10.1186/2050-490X-1-5
Yi Wang, Chaoshu Tang, Yanwen Qin
{"title":"组织蛋白酶:腹主动脉瘤背后的新罪魁祸首。","authors":"Yi Wang,&nbsp;Chaoshu Tang,&nbsp;Yanwen Qin","doi":"10.1186/2050-490X-1-5","DOIUrl":null,"url":null,"abstract":"<p><p>Abdominal aortic aneurysm (AAA) is a fatal disease defined as an abdominal aortic diameter of 3.0 cm or more, where the abdominal aorta exceeds the normal diameter by more than 50%. Histopathological changes of AAA mainly include extracellular matrix (ECM) remodeling at the abdominal aorta wall, but there is lack of specific drugs to treat AAA. Recent studies have reported that lysosomal cathepsins could induce vascular remodeling and AAA formation by regulating vascular inflammation, medial smooth muscle cell apoptosis, neovascularization, and protease expression. Thus, cathepsins are expected to become a new therapeutic target for AAA treatment. </p>","PeriodicalId":42378,"journal":{"name":"Regenerative Medicine Research","volume":null,"pages":null},"PeriodicalIF":2.0000,"publicationDate":"2013-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/2050-490X-1-5","citationCount":"14","resultStr":"{\"title\":\"Cathepsins: a new culprit behind abdominal aortic aneurysm.\",\"authors\":\"Yi Wang,&nbsp;Chaoshu Tang,&nbsp;Yanwen Qin\",\"doi\":\"10.1186/2050-490X-1-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Abdominal aortic aneurysm (AAA) is a fatal disease defined as an abdominal aortic diameter of 3.0 cm or more, where the abdominal aorta exceeds the normal diameter by more than 50%. Histopathological changes of AAA mainly include extracellular matrix (ECM) remodeling at the abdominal aorta wall, but there is lack of specific drugs to treat AAA. Recent studies have reported that lysosomal cathepsins could induce vascular remodeling and AAA formation by regulating vascular inflammation, medial smooth muscle cell apoptosis, neovascularization, and protease expression. Thus, cathepsins are expected to become a new therapeutic target for AAA treatment. </p>\",\"PeriodicalId\":42378,\"journal\":{\"name\":\"Regenerative Medicine Research\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2013-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1186/2050-490X-1-5\",\"citationCount\":\"14\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Regenerative Medicine Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1186/2050-490X-1-5\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2013/12/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Regenerative Medicine Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/2050-490X-1-5","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2013/12/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 14

摘要

腹主动脉瘤(AAA)是一种致命的疾病,定义为腹主动脉直径大于或等于3.0 cm,其中腹主动脉直径超过正常直径的50%以上。AAA的组织病理改变主要表现为腹主动脉壁的细胞外基质(extracellular matrix, ECM)重构,但目前缺乏特异性药物治疗AAA。近年研究报道溶酶体组织蛋白酶可通过调节血管炎症、内侧平滑肌细胞凋亡、新生血管形成和蛋白酶表达,诱导血管重构和AAA形成。因此,组织蛋白酶有望成为AAA治疗的新靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Cathepsins: a new culprit behind abdominal aortic aneurysm.

Abdominal aortic aneurysm (AAA) is a fatal disease defined as an abdominal aortic diameter of 3.0 cm or more, where the abdominal aorta exceeds the normal diameter by more than 50%. Histopathological changes of AAA mainly include extracellular matrix (ECM) remodeling at the abdominal aorta wall, but there is lack of specific drugs to treat AAA. Recent studies have reported that lysosomal cathepsins could induce vascular remodeling and AAA formation by regulating vascular inflammation, medial smooth muscle cell apoptosis, neovascularization, and protease expression. Thus, cathepsins are expected to become a new therapeutic target for AAA treatment.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Regenerative Medicine Research
Regenerative Medicine Research MEDICINE, RESEARCH & EXPERIMENTAL-
自引率
0.00%
发文量
0
审稿时长
6 weeks
期刊最新文献
The effectiveness of mineralized plasmatic matrix in the closure of alveolar clefts with volumetric assessment. Liver regeneration in traditional Chinese medicine: advances and challenges. Siwei Jianbu decoction improves painful paclitaxel-induced peripheral neuropathy in mouse model by modulating the NF-κB and MAPK signaling pathways. Quality comparison between two different types of platelet-rich plasma for knee osteoarthritis. Implant-type tissue-engineered cartilage derived from human auricular chondrocyte may maintain cartilaginous property even under osteoinductive condition.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1