• 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

非胰岛素依赖型糖尿病发病机制的转基因研究方法。

Transgenic approaches to the pathogenesis of NIDDM.

作者信息

Moller D E

机构信息

Department of Medicine, Harvard Medical School, Boston, Massachusetts.

出版信息

Diabetes. 1994 Dec;43(12):1394-401. doi: 10.2337/diab.43.12.1394.

DOI:10.2337/diab.43.12.1394
PMID:7958489
Abstract

The pathogenesis of non-insulin-dependent diabetes mellitus (NIDDM) involves complex interactions between multiple physiological defects, both genetic and acquired. The application of transgenic technology to create animal models that address questions concerning NIDDM (and obesity) is a very recent development that is now gaining rapid momentum and receiving deserved attention. In general, transgenic methods afford new opportunities to alter the site or level of expression of functional genes in vivo, to transfer novel foreign genes into animals, to prevent the expression of specific genes, or to replace genes with specific genetic variants. Two general approaches can be applied: 1) conventional transgenics, the transfer to and expression of new genetic information in animals; and 2) gene targeting, the disruption or replacement of specific endogenous genes. Recent transgenic initiatives have provided important insights into 1) the mechanism of glucose-stimulated insulin secretion and the role of potential defects in this system, 2) the regulated expression of genes that control hepatic glucose production, 3) the role of specific molecules that mediate the actions of insulin, and 4) the elucidation of factors that contribute to in vivo regulation of energy balance and body composition. Emerging transgenic strategies should have a dramatic impact on future efforts to assess the function of newly identified molecules implicated in the regulation of in vivo glucose homeostasis and to determine the roles of candidate loci or specific mutations uncovered during the search for new NIDDM susceptibility genes.

摘要

非胰岛素依赖型糖尿病(NIDDM)的发病机制涉及多种生理缺陷之间复杂的相互作用,这些缺陷既有遗传的,也有后天获得的。应用转基因技术创建动物模型来解决与NIDDM(及肥胖症)相关的问题是一项非常新的进展,目前正迅速发展并受到应有的关注。一般来说,转基因方法为在体内改变功能基因的表达位点或水平、将新的外源基因导入动物、阻止特定基因的表达或用特定的基因变体替换基因提供了新的机会。可应用两种一般方法:1)传统转基因,即将新的遗传信息导入动物并使其表达;2)基因打靶,即破坏或替换特定的内源基因。最近的转基因研究为以下方面提供了重要见解:1)葡萄糖刺激的胰岛素分泌机制以及该系统潜在缺陷的作用;2)控制肝葡萄糖生成的基因的调节表达;3)介导胰岛素作用的特定分子的作用;4)阐明体内能量平衡和身体组成调节的影响因素。新兴的转基因策略应对未来评估新发现的与体内葡萄糖稳态调节有关的分子功能以及确定在寻找新的NIDDM易感基因过程中发现的候选基因座或特定突变的作用的努力产生重大影响。

相似文献

1
Transgenic approaches to the pathogenesis of NIDDM.非胰岛素依赖型糖尿病发病机制的转基因研究方法。
Diabetes. 1994 Dec;43(12):1394-401. doi: 10.2337/diab.43.12.1394.
2
Genetic manipulation of insulin signaling, action and secretion in mice. Insights into glucose homeostasis and pathogenesis of type 2 diabetes.小鼠胰岛素信号传导、作用及分泌的基因操作。对葡萄糖稳态及2型糖尿病发病机制的见解。
EMBO Rep. 2002 Apr;3(4):323-8. doi: 10.1093/embo-reports/kvf078.
3
The genetics of human noninsulin-dependent (type 2) diabetes mellitus.人类非胰岛素依赖型(2型)糖尿病的遗传学
J Nutr. 1997 Sep;127(9):1891S-1896S. doi: 10.1093/jn/127.9.1891S.
4
Non-insulin-dependent diabetes mellitus--a collision between thrifty genes and an affluent society.非胰岛素依赖型糖尿病——节俭基因与富足社会之间的冲突。
Ann Med. 1997 Feb;29(1):37-53. doi: 10.3109/07853899708998742.
5
On the pathophysiology of late onset non-insulin dependent diabetes mellitus. Current controversies and new insights.关于晚发型非胰岛素依赖型糖尿病的病理生理学。当前的争议与新见解。
Dan Med Bull. 1999 Jun;46(3):197-234.
6
Are animal models of diabetes relevant to the study of the genetics of non-insulin-dependent diabetes in humans?糖尿病动物模型与人类非胰岛素依赖型糖尿病遗传学研究相关吗?
Diabetes Metab. 1997 Mar;23 Suppl 2:38-46.
7
Transgenic mice overexpressing insulin-like growth factor-II in beta cells develop type 2 diabetes.在β细胞中过表达胰岛素样生长因子-II的转基因小鼠会患2型糖尿病。
J Clin Invest. 2000 Mar;105(6):731-40. doi: 10.1172/JCI5656.
8
Lilly Lecture 1994. The beta-cell in diabetes: from molecular genetics to clinical research.1994年礼来讲座。糖尿病中的β细胞:从分子遗传学到临床研究。
Diabetes. 1995 Jun;44(6):705-17. doi: 10.2337/diab.44.6.705.
9
Cellular engineering and gene therapy strategies for insulin replacement in diabetes.糖尿病胰岛素替代的细胞工程和基因治疗策略
Diabetes. 1994 Mar;43(3):341-50. doi: 10.2337/diab.43.3.341.
10
Lessons from transgenic and knockout animals about noninsulin-dependent diabetes mellitus.
Trends Endocrinol Metab. 1996 Nov;7(9):311-9. doi: 10.1016/s1043-2760(96)00154-3.

引用本文的文献

1
Ins1(Cre) knock-in mice for beta cell-specific gene recombination.用于β细胞特异性基因重组的Ins1(Cre)敲入小鼠。
Diabetologia. 2015 Mar;58(3):558-65. doi: 10.1007/s00125-014-3468-5. Epub 2014 Dec 11.
2
Insights into insulin resistance and type 2 diabetes from knockout mouse models.从基因敲除小鼠模型深入了解胰岛素抵抗和2型糖尿病
J Clin Invest. 2000 Aug;106(4):459-65. doi: 10.1172/JCI10830.
3
Genetic engineering in mice: impact on insulin signalling and action.小鼠中的基因工程:对胰岛素信号传导及作用的影响。
Biochem J. 1998 Oct 15;335 ( Pt 2)(Pt 2):193-204. doi: 10.1042/bj3350193.
4
Genetic manipulation of insulin action and beta-cell function in mice.小鼠胰岛素作用和β细胞功能的基因操纵
Mol Cell Biochem. 1998 May;182(1-2):161-8.
5
Targeted disruption of the insulin receptor gene in the mouse results in neonatal lethality.小鼠胰岛素受体基因的靶向破坏导致新生期致死。
EMBO J. 1996 Apr 1;15(7):1542-7.