• 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

强大的小鼠:转基因技术“敲除”基质金属蛋白酶功能问题。

Mighty mice: transgenic technology "knocks out" questions of matrix metalloproteinase function.

作者信息

Shapiro S D

机构信息

Department of Medicine, Washington University School of Medicine, Barnes Jewish Hospital, St. Louis, Missouri, USA.

出版信息

Matrix Biol. 1997 Mar;15(8-9):527-33. doi: 10.1016/s0945-053x(97)90027-5.

DOI:10.1016/s0945-053x(97)90027-5
PMID:9138285
Abstract

Matrix metalloproteinases (MMP) comprise a family of structurally related proteinases that are believed to play a critical role in many physiological and pathological processes. Transgenic technology offers the possibility of determining whether MMPs contribute directly to these processes. For example, gain of function and loss of function models have confirmed causative roles of MMPs in the development of pulmonary emphysema and unexpectedly uncovered an MMP-dependent mechanism of inflammatory cell recruitment. Limitations of these techniques and powerful applications on the horizon are also presented as we embark on an era where controlled experiments can be performed in complex mammalian models.

摘要

基质金属蛋白酶(MMP)是一类结构相关的蛋白酶家族,据信在许多生理和病理过程中发挥关键作用。转基因技术为确定MMP是否直接参与这些过程提供了可能性。例如,功能获得和功能丧失模型已证实MMP在肺气肿发展中的致病作用,并且意外地发现了一种依赖MMP的炎症细胞募集机制。随着我们迈入一个可以在复杂哺乳动物模型中进行对照实验的时代,还介绍了这些技术的局限性以及即将出现的强大应用。

相似文献

1
Mighty mice: transgenic technology "knocks out" questions of matrix metalloproteinase function.强大的小鼠:转基因技术“敲除”基质金属蛋白酶功能问题。
Matrix Biol. 1997 Mar;15(8-9):527-33. doi: 10.1016/s0945-053x(97)90027-5.
2
Overexpression of matrix metalloproteinases leads to lethality in transgenic Xenopus laevis: implications for tissue-dependent functions of matrix metalloproteinases during late embryonic development.基质金属蛋白酶的过表达导致转基因非洲爪蟾死亡:对胚胎发育后期基质金属蛋白酶组织依赖性功能的启示。
Dev Dyn. 2001 May;221(1):37-47. doi: 10.1002/dvdy.1123.
3
[Matrix metalloproteinase (MMP)].
C R Seances Soc Biol Fil. 1991;185(3):127-34.
4
MT1-MMP-dependent neovessel formation within the confines of the three-dimensional extracellular matrix.MT1-基质金属蛋白酶依赖性新血管在三维细胞外基质范围内形成。
J Cell Biol. 2004 Nov 22;167(4):757-67. doi: 10.1083/jcb.200405001. Epub 2004 Nov 15.
5
Coordinate expression of matrix metalloproteinase family members in the uterus of normal, matrilysin-deficient, and stromelysin-1-deficient mice.正常小鼠、基质溶素缺陷小鼠和基质溶解素-1缺陷小鼠子宫中基质金属蛋白酶家族成员的协同表达
Endocrinology. 1997 Nov;138(11):4902-11. doi: 10.1210/endo.138.11.5478.
6
Matrix metalloproteinases and their inhibitors regulate in vitro ureteric bud branching morphogenesis.基质金属蛋白酶及其抑制剂调节体外输尿管芽分支形态发生。
Am J Physiol Renal Physiol. 2000 Nov;279(5):F891-900. doi: 10.1152/ajprenal.2000.279.5.F891.
7
Matrix metalloproteinases (MMPs) regulate fibrin-invasive activity via MT1-MMP-dependent and -independent processes.基质金属蛋白酶(MMPs)通过MT1-MMP依赖性和非依赖性过程调节纤维蛋白侵袭活性。
J Exp Med. 2002 Feb 4;195(3):295-308. doi: 10.1084/jem.20010815.
8
Utilization of transgenic mice in the study of matrix degrading proteinases and their inhibitors.转基因小鼠在基质降解蛋白酶及其抑制剂研究中的应用。
Cancer Metastasis Rev. 1995 Jun;14(2):97-111. doi: 10.1007/BF00665794.
9
Roles of the matrix metalloproteinases in mammary gland development and cancer.
Breast Cancer Res Treat. 1998 Jul;50(2):97-116. doi: 10.1023/a:1006061115909.
10
Matrix metalloproteinase-12 (MMP-12) in osteoclasts: new lesson on the involvement of MMPs in bone resorption.破骨细胞中的基质金属蛋白酶-12(MMP-12):基质金属蛋白酶参与骨吸收的新认识。
Bone. 2004 Jan;34(1):37-47. doi: 10.1016/j.bone.2003.08.011.

引用本文的文献

1
[COPD: An early disease].[慢性阻塞性肺疾病:一种早期疾病]
Rev Pneumol Clin. 2016 Feb;72(1):49-60. doi: 10.1016/j.pneumo.2015.08.002. Epub 2015 Dec 3.
2
Chronic obstructive pulmonary disease * 3: Experimental animal models of pulmonary emphysema.慢性阻塞性肺疾病*3:肺气肿的实验动物模型
Thorax. 2002 Oct;57(10):908-14. doi: 10.1136/thorax.57.10.908.
3
Animal models of chronic obstructive pulmonary disease.慢性阻塞性肺疾病的动物模型
Thorax. 2001 Dec;56(12):972-7. doi: 10.1136/thorax.56.12.972.
4
Regulation of membrane-type matrix metalloproteinase 1 activity by dynamin-mediated endocytosis.发动蛋白介导的内吞作用对膜型基质金属蛋白酶1活性的调控
Proc Natl Acad Sci U S A. 2001 Nov 20;98(24):13693-8. doi: 10.1073/pnas.241293698. Epub 2001 Nov 6.
5
The clinical potential of matrix metalloproteinase inhibitors in the rheumatic disorders.基质金属蛋白酶抑制剂在风湿性疾病中的临床潜力。
Drugs Aging. 2001;18(2):87-99. doi: 10.2165/00002512-200118020-00002.
6
Gelatinase B (MMP-9) is not essential in the normal kidney and does not influence progression of renal disease in a mouse model of Alport syndrome.明胶酶B(基质金属蛋白酶-9)在正常肾脏中并非必需,并且在阿尔波特综合征小鼠模型中不影响肾脏疾病的进展。
Am J Pathol. 2000 Jul;157(1):303-11. doi: 10.1016/S0002-9440(10)64541-5.
7
Matrix metalloproteinase biology applied to vitreoretinal disorders.应用于玻璃体视网膜疾病的基质金属蛋白酶生物学
Br J Ophthalmol. 2000 Jun;84(6):654-66. doi: 10.1136/bjo.84.6.654.
8
Recent advances in molecular biological techniques and their relevance to pulmonary research.分子生物学技术的最新进展及其与肺部研究的相关性。
Thorax. 2000 Apr;55(4):329-39. doi: 10.1136/thorax.55.4.329.
9
Resistance of young gelatinase B-deficient mice to experimental autoimmune encephalomyelitis and necrotizing tail lesions.年轻的明胶酶B缺陷小鼠对实验性自身免疫性脑脊髓炎和坏死性尾部病变的抵抗力。
J Clin Invest. 1999 Dec;104(11):1507-15. doi: 10.1172/JCI6886.