• 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

胰腺β细胞中细胞周期进程的分子调控

Molecular control of cell cycle progression in the pancreatic beta-cell.

作者信息

Cozar-Castellano Irene, Fiaschi-Taesch Nathalie, Bigatel Todd A, Takane Karen K, Garcia-Ocaña Adolfo, Vasavada Rupangi, Stewart Andrew F

机构信息

Division of Endocrinology and Metabolism, BST E-1140, The University of Pittsburgh School of Medicine, 200 Lothrop Street, Pennsylvania 15213, USA.

出版信息

Endocr Rev. 2006 Jun;27(4):356-70. doi: 10.1210/er.2006-0004. Epub 2006 Apr 25.

DOI:10.1210/er.2006-0004
PMID:16638909
Abstract

Type 1 and type 2 diabetes both result from inadequate production of insulin by the beta-cells of the pancreatic islet. Accordingly, strategies that lead to increased pancreatic beta-cell mass, as well as retained or enhanced function of islets, would be desirable for the treatment of diabetes. Although pancreatic beta-cells have long been viewed as terminally differentiated and irreversibly arrested, evidence now indicates that beta-cells can and do replicate, that this replication can be enhanced by a variety of maneuvers, and that beta-cell replication plays a quantitatively significant role in maintaining pancreatic beta-cell mass and function. Because beta-cells have been viewed as being unable to proliferate, the science of beta-cell replication is undeveloped. In the past several years, however, this has begun to change at a rapid pace, and many laboratories are now focused on elucidating the molecular details of the control of cell cycle in the beta-cell. In this review, we review the molecular details of cell cycle control as they relate to the pancreatic beta-cell. Our hope is that this review can serve as a common basis and also a roadmap for those interested in developing novel strategies for enhancing beta-cell replication and improving insulin production in animal models as well as in human pancreatic beta-cells.

摘要

1型糖尿病和2型糖尿病均源于胰岛β细胞胰岛素分泌不足。因此,增加胰腺β细胞数量以及维持或增强胰岛功能的策略对于糖尿病治疗而言是可取的。尽管长期以来人们一直认为胰腺β细胞是终末分化且不可逆停滞的,但现在有证据表明β细胞能够且确实可以复制,这种复制可通过多种手段增强,并且β细胞复制在维持胰腺β细胞数量和功能方面发挥着重要的定量作用。由于β细胞一直被认为无法增殖,β细胞复制的科学研究尚不发达。然而,在过去几年中,这种情况已开始迅速改变,许多实验室现在专注于阐明β细胞中细胞周期调控的分子细节。在本综述中,我们回顾与胰腺β细胞相关的细胞周期调控的分子细节。我们希望这篇综述能够成为一个共同的基础,同时也为那些有兴趣在动物模型以及人类胰腺β细胞中开发增强β细胞复制和改善胰岛素分泌新策略的人提供一个路线图。

相似文献

1
Molecular control of cell cycle progression in the pancreatic beta-cell.胰腺β细胞中细胞周期进程的分子调控
Endocr Rev. 2006 Jun;27(4):356-70. doi: 10.1210/er.2006-0004. Epub 2006 Apr 25.
2
BCL-x(L) and BCL2 delay Myc-induced cell cycle entry through elevation of p27 and inhibition of G1 cyclin-dependent kinases.BCL-x(L)和BCL2通过提高p27水平并抑制G1期细胞周期蛋白依赖性激酶来延迟Myc诱导的细胞周期进入。
Oncogene. 2002 Nov 7;21(51):7765-75. doi: 10.1038/sj.onc.1205928.
3
Aberrant cell cycle regulation in cervical carcinoma.子宫颈癌中的异常细胞周期调控。
Yonsei Med J. 2005 Oct 31;46(5):597-613. doi: 10.3349/ymj.2005.46.5.597.
4
Regulation of beta cell replication.β细胞复制的调控
Mol Cell Endocrinol. 2009 Jan 15;297(1-2):18-27. doi: 10.1016/j.mce.2008.08.033. Epub 2008 Sep 7.
5
BCR signals target p27(Kip1) and cyclin D2 via the PI3-K signalling pathway to mediate cell cycle arrest and apoptosis of WEHI 231 B cells.BCR信号通过PI3-K信号通路靶向p27(Kip1)和细胞周期蛋白D2,以介导WEHI 231 B细胞的细胞周期停滞和凋亡。
Oncogene. 2001 Nov 1;20(50):7352-67. doi: 10.1038/sj.onc.1204951.
6
Differential control of cyclins D1 and D3 and the cdk inhibitor p27Kip1 by diverse signalling pathways in Swiss 3T3 cells.瑞士3T3细胞中不同信号通路对细胞周期蛋白D1和D3以及细胞周期蛋白依赖性激酶抑制剂p27Kip1的差异调控
Oncogene. 1997 Apr 17;14(15):1759-66. doi: 10.1038/sj.onc.1201134.
7
Cell cycle control of pancreatic beta cell proliferation.胰腺β细胞增殖的细胞周期调控
Front Biosci. 2000 Jan 1;5:D1-19. doi: 10.2741/rane.
8
New insights into cyclins, CDKs, and cell cycle control.细胞周期蛋白、细胞周期蛋白依赖性激酶与细胞周期调控的新见解
Semin Cell Dev Biol. 2005 Jun;16(3):311-21. doi: 10.1016/j.semcdb.2005.02.007.
9
[Cycling without D-type cyclin].[无D型细胞周期蛋白的细胞周期运转]
Med Sci (Paris). 2005 Jan;21(1):19-22. doi: 10.1051/medsci/200521119.
10
Expression and activity of the retinoblastoma protein (pRB)-family proteins, p107 and p130, during L6 myoblast differentiation.视网膜母细胞瘤蛋白(pRB)家族蛋白p107和p130在L6成肌细胞分化过程中的表达与活性
Cell Growth Differ. 1995 Oct;6(10):1287-98.

引用本文的文献

1
Multi-omic human pancreatic islet endoplasmic reticulum and cytokine stress response mapping provides type 2 diabetes genetic insights.多组学人类胰腺胰岛内质网和细胞因子应激反应图谱为 2 型糖尿病的遗传见解提供了依据。
Cell Metab. 2024 Nov 5;36(11):2468-2488.e7. doi: 10.1016/j.cmet.2024.09.006. Epub 2024 Oct 8.
2
Sulforaphane Ameliorates High-Fat-Diet-Induced Metabolic Abnormalities in Young and Middle-Aged Obese Male Mice.萝卜硫素改善高脂饮食诱导的中青年肥胖雄性小鼠代谢异常
Foods. 2024 Mar 29;13(7):1055. doi: 10.3390/foods13071055.
3
An olive-derived elenolic acid stimulates hormone release from L-cells and exerts potent beneficial metabolic effects in obese diabetic mice.
一种源自橄榄的橄榄烯酸可刺激L细胞释放激素,并对肥胖糖尿病小鼠产生强大的有益代谢作用。
Front Nutr. 2022 Nov 1;9:1051452. doi: 10.3389/fnut.2022.1051452. eCollection 2022.
4
The Transcription Factor YY1 Is Essential for Normal DNA Repair and Cell Cycle in Human and Mouse β-Cells.转录因子 YY1 对于人和小鼠β细胞的正常 DNA 修复和细胞周期至关重要。
Diabetes. 2022 Aug 1;71(8):1694-1705. doi: 10.2337/db21-0908.
5
Candidate master microRNA regulator of arsenic-induced pancreatic beta cell impairment revealed by multi-omics analysis.通过多组学分析揭示候选 miRNA 调控剂在砷诱导的胰腺β细胞损伤中的作用。
Arch Toxicol. 2022 Jun;96(6):1685-1699. doi: 10.1007/s00204-022-03263-9. Epub 2022 Mar 21.
6
Regenerative approaches to preserve pancreatic β-cell mass and function in diabetes pathogenesis.在糖尿病发病机制中,再生方法可用于保护胰腺β细胞的数量和功能。
Endocrine. 2022 Feb;75(2):338-350. doi: 10.1007/s12020-021-02941-5. Epub 2021 Nov 25.
7
β-Arrestin-1 is required for adaptive β-cell mass expansion during obesity.β-arrestin-1 在肥胖期间适应β细胞质量扩张中是必需的。
Nat Commun. 2021 Jun 7;12(1):3385. doi: 10.1038/s41467-021-23656-1.
8
The Human Islet: Mini-Organ With Mega-Impact.人类胰岛:迷你器官,巨大影响。
Endocr Rev. 2021 Sep 28;42(5):605-657. doi: 10.1210/endrev/bnab010.
9
CDK2 limits the highly energetic secretory program of mature β cells by restricting PEP cycle-dependent K channel closure.CDK2 通过限制 PEP 周期依赖性钾通道关闭来限制成熟β细胞的高能量分泌程序。
Cell Rep. 2021 Jan 26;34(4):108690. doi: 10.1016/j.celrep.2021.108690.
10
Inhibition of oxidative metabolism by nitric oxide restricts EMCV replication selectively in pancreatic beta-cells.一氧化氮抑制氧化代谢可选择性地限制胰腺β细胞中 EMCV 的复制。
J Biol Chem. 2020 Dec 25;295(52):18189-18198. doi: 10.1074/jbc.RA120.015893. Epub 2020 Oct 25.