• 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

相似文献

1
Overexpression of Pref-1 in pancreatic islet β-cells in mice causes hyperinsulinemia with increased islet mass and insulin secretion.小鼠胰岛β细胞中Pref-1的过表达会导致高胰岛素血症,同时胰岛质量和胰岛素分泌增加。
Biochem Biophys Res Commun. 2015 Jun 12;461(4):630-5. doi: 10.1016/j.bbrc.2015.04.078. Epub 2015 Apr 24.
2
Insulin hypersecretion in islets from diet-induced hyperinsulinemic obese female mice is associated with several functional adaptations in individual β-cells.饮食诱导的肥胖雌性小鼠胰岛中胰岛素的过度分泌与个体β细胞的几种功能适应性有关。
Endocrinology. 2013 Oct;154(10):3515-24. doi: 10.1210/en.2013-1424. Epub 2013 Jul 18.
3
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.
4
Glucose homeostasis, insulin secretion, and islet phospholipids in mice that overexpress iPLA2beta in pancreatic beta-cells and in iPLA2beta-null mice.胰腺β细胞中过表达iPLA2β的小鼠以及iPLA2β基因敲除小鼠的葡萄糖稳态、胰岛素分泌和胰岛磷脂
Am J Physiol Endocrinol Metab. 2008 Feb;294(2):E217-29. doi: 10.1152/ajpendo.00474.2007. Epub 2007 Sep 25.
5
Glucose intolerance and reduced islet blood flow in transgenic mice expressing the FRK tyrosine kinase under the control of the rat insulin promoter.在大鼠胰岛素启动子控制下表达FRK酪氨酸激酶的转基因小鼠中,葡萄糖耐量异常及胰岛血流减少。
Am J Physiol Endocrinol Metab. 2007 Apr;292(4):E1183-90. doi: 10.1152/ajpendo.00168.2006. Epub 2006 Dec 19.
6
Expression, biosynthesis and release of preadipocyte factor-1/ delta-like protein/fetal antigen-1 in pancreatic beta-cells: possible physiological implications.前脂肪细胞因子-1/δ样蛋白/胎儿抗原-1在胰腺β细胞中的表达、生物合成及释放:可能的生理意义
J Endocrinol. 2003 Feb;176(2):257-66. doi: 10.1677/joe.0.1760257.
7
Overexpression of parathyroid hormone-related protein in the pancreatic islets of transgenic mice causes islet hyperplasia, hyperinsulinemia, and hypoglycemia.转基因小鼠胰岛中甲状旁腺激素相关蛋白的过表达会导致胰岛增生、高胰岛素血症和低血糖。
J Biol Chem. 1996 Jan 12;271(2):1200-8. doi: 10.1074/jbc.271.2.1200.
8
Early and rapid development of insulin resistance, islet dysfunction and glucose intolerance after high-fat feeding in mice overexpressing phosphodiesterase 3B.在过表达磷酸二酯酶3B的小鼠中,高脂喂养后胰岛素抵抗、胰岛功能障碍和葡萄糖耐量异常会早期快速发展。
J Endocrinol. 2006 Jun;189(3):629-41. doi: 10.1677/joe.1.06522.
9
Preadipocyte factor 1 induces pancreatic ductal cell differentiation into insulin-producing cells.前脂肪细胞因子1诱导胰腺导管细胞分化为胰岛素分泌细胞。
Sci Rep. 2016 Apr 5;6:23960. doi: 10.1038/srep23960.
10
Postnatal development of numbers and mean sizes of pancreatic islets and beta-cells in healthy mice and GIPR(dn) transgenic diabetic mice.健康小鼠和 GIPR(dn) 转基因糖尿病小鼠胰岛和β细胞数量及平均大小的产后发育。
PLoS One. 2011;6(7):e22814. doi: 10.1371/journal.pone.0022814. Epub 2011 Jul 26.

引用本文的文献

1
Untangling the genetics of beta cell dysfunction and death in type 1 diabetes.解析 1 型糖尿病中β细胞功能障碍和死亡的遗传学。
Mol Metab. 2024 Aug;86:101973. doi: 10.1016/j.molmet.2024.101973. Epub 2024 Jun 22.
2
The Transcriptome and Epigenome Reveal Novel Changes in Transcription Regulation During Pancreatic Rat Islet Maturation.《转录组和表观基因组揭示了胰腺大鼠胰岛成熟过程中转录调控的新变化》
Endocrinology. 2021 Nov 1;162(11). doi: 10.1210/endocr/bqab181.
3
Imprinted Genes Impact Upon Beta Cell Function in the Current (and Potentially Next) Generation.印迹基因对当前(及未来)代β细胞功能的影响。
Front Endocrinol (Lausanne). 2021 Apr 27;12:660532. doi: 10.3389/fendo.2021.660532. eCollection 2021.
4
Identification of type 2 diabetes loci in 433,540 East Asian individuals.在 433,540 名东亚个体中鉴定 2 型糖尿病基因座。
Nature. 2020 Jun;582(7811):240-245. doi: 10.1038/s41586-020-2263-3. Epub 2020 May 6.
5
promoter in human pancreatic β cells contacts diabetes susceptibility loci and regulates genes affecting insulin metabolism.在人类胰腺β细胞中,启动子与糖尿病易感性位点接触,并调节影响胰岛素代谢的基因。
Proc Natl Acad Sci U S A. 2018 May 15;115(20):E4633-E4641. doi: 10.1073/pnas.1803146115. Epub 2018 Apr 30.
6
Identification of the MUC2 Promoter as a Strong Promoter for Intestinal Gene Expression through Generation of Transgenic Quail Expressing GFP in Gut Epithelial Cells.通过生成在肠道上皮细胞中表达绿色荧光蛋白的转基因鹌鹑来鉴定MUC2启动子作为肠道基因表达的强启动子。
Int J Mol Sci. 2017 Jan 19;18(1):196. doi: 10.3390/ijms18010196.
7
Age-Dependent Pancreatic Gene Regulation Reveals Mechanisms Governing Human β Cell Function.年龄依赖性胰腺基因调控揭示了人类β细胞功能的调控机制。
Cell Metab. 2016 May 10;23(5):909-20. doi: 10.1016/j.cmet.2016.04.002. Epub 2016 Apr 28.

本文引用的文献

1
Pref-1 marks very early mesenchymal precursors required for adipose tissue development and expansion.Pref-1标记了脂肪组织发育和扩张所需的非常早期的间充质前体细胞。
Cell Rep. 2014 Aug 7;8(3):678-87. doi: 10.1016/j.celrep.2014.06.060. Epub 2014 Jul 31.
2
Pref-1 interacts with fibronectin to inhibit adipocyte differentiation.Pref-1 与纤连蛋白相互作用,抑制脂肪细胞分化。
Mol Cell Biol. 2010 Jul;30(14):3480-92. doi: 10.1128/MCB.00057-10. Epub 2010 May 10.
3
Pref-1 regulates mesenchymal cell commitment and differentiation through Sox9.Pref-1通过Sox9调节间充质细胞的定向分化。
Cell Metab. 2009 Mar;9(3):287-302. doi: 10.1016/j.cmet.2009.01.013.
4
Resistance to high-fat diet-induced obesity but exacerbated insulin resistance in mice overexpressing preadipocyte factor-1 (Pref-1): a new model of partial lipodystrophy.过表达前脂肪细胞因子-1(Pref-1)的小鼠对高脂饮食诱导的肥胖具有抗性,但胰岛素抵抗加剧:一种部分脂肪营养不良的新模型。
Diabetes. 2008 Dec;57(12):3258-66. doi: 10.2337/db07-1739. Epub 2008 Oct 3.
5
Pref-1 (preadipocyte factor 1) activates the MEK/extracellular signal-regulated kinase pathway to inhibit adipocyte differentiation.前脂肪细胞因子1(Pref-1)激活MEK/细胞外信号调节激酶通路以抑制脂肪细胞分化。
Mol Cell Biol. 2007 Mar;27(6):2294-308. doi: 10.1128/MCB.02207-06. Epub 2007 Jan 8.
6
Ectodomain shedding of preadipocyte factor 1 (Pref-1) by tumor necrosis factor alpha converting enzyme (TACE) and inhibition of adipocyte differentiation.肿瘤坏死因子α转换酶(TACE)介导的前脂肪细胞因子1(Pref-1)胞外域脱落与脂肪细胞分化的抑制
Mol Cell Biol. 2006 Jul;26(14):5421-35. doi: 10.1128/MCB.02437-05.
7
Inhibition of adipogenesis and development of glucose intolerance by soluble preadipocyte factor-1 (Pref-1).可溶性前脂肪细胞因子-1(Pref-1)对脂肪生成的抑制作用及葡萄糖不耐受的发展
J Clin Invest. 2003 Feb;111(4):453-61. doi: 10.1172/JCI15924.
8
Mice lacking paternally expressed Pref-1/Dlk1 display growth retardation and accelerated adiposity.缺乏父系表达的Pref-1/Dlk1的小鼠表现出生长迟缓以及肥胖加剧。
Mol Cell Biol. 2002 Aug;22(15):5585-92. doi: 10.1128/MCB.22.15.5585-5592.2002.
9
Only the large soluble form of preadipocyte factor-1 (Pref-1), but not the small soluble and membrane forms, inhibits adipocyte differentiation: role of alternative splicing.只有前脂肪细胞因子-1(Pref-1)的大的可溶性形式,而非小的可溶性形式和膜结合形式,能抑制脂肪细胞分化:可变剪接的作用。
Biochem J. 2002 May 15;364(Pt 1):137-44. doi: 10.1042/bj3640137.
10
Delta-like and gtl2 are reciprocally expressed, differentially methylated linked imprinted genes on mouse chromosome 12.Delta样基因和gtl2是位于小鼠12号染色体上相互表达、差异甲基化的连锁印记基因。
Curr Biol. 2000 Sep 21;10(18):1135-8. doi: 10.1016/s0960-9822(00)00704-1.

小鼠胰岛β细胞中Pref-1的过表达会导致高胰岛素血症,同时胰岛质量和胰岛素分泌增加。

Overexpression of Pref-1 in pancreatic islet β-cells in mice causes hyperinsulinemia with increased islet mass and insulin secretion.

作者信息

Wang Yuhui, Lee Kichoon, Moon Yang Soo, Ahmadian Maryam, Kim Kee-Hong, Roder Karim, Kang Chulho, Sul Hei Sook

机构信息

Department of Nutritional Sciences and Toxicology, University of California, Berkeley, CA 94720, USA.

Department of Molecular Cell Biology, University of California, Berkeley, CA 94720, USA.

出版信息

Biochem Biophys Res Commun. 2015 Jun 12;461(4):630-5. doi: 10.1016/j.bbrc.2015.04.078. Epub 2015 Apr 24.

DOI:10.1016/j.bbrc.2015.04.078
PMID:25918019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4439292/
Abstract

Preadipocyte factor-1 (Pref-1) is made as a transmembrane protein containing EGF-repeats at the extracellular domain that can be cleaved to generate a biologically active soluble form. Pref-1 is found in islet β-cells and its level has been reported to increase in neonatal rat islets upon growth hormone treatment. We found here that Pref-1 can promote growth of pancreatic tumor derived AR42J cells. To examine Pref-1 function in pancreatic islets in vivo, we generated transgenic mouse lines overexpressing the Pref-1/hFc in islet β-cells using rat insulin II promoter (RIP). These transgenic mice exhibit an increase in islet mass with higher proportion of larger islets in pancreas compared to wild-type littermates. This is in contrast to pancreas from Pref-1 null mice that show higher proportion of smaller islets. Insulin expression and insulin secretion from pancreatic islets from RIP-Pref-1/hFc transgenic mice are increased also. Thus, RIP-Pref-1/hFc transgenic mice show normal glucose levels but with higher plasma insulin levels in both fasting and fed conditions. These mice show improved glucose tolerance. Taken together, we conclude Pref-1 as a positive regulator of islet β-cells and insulin production.

摘要

前脂肪细胞因子-1(Pref-1)最初是一种跨膜蛋白,其胞外结构域含有表皮生长因子(EGF)重复序列,该序列可被切割以产生具有生物活性的可溶性形式。Pref-1存在于胰岛β细胞中,据报道,在生长激素处理后,新生大鼠胰岛中Pref-1的水平会升高。我们在此发现,Pref-1可促进胰腺肿瘤来源的AR42J细胞的生长。为了在体内研究Pref-1在胰岛中的功能,我们使用大鼠胰岛素II启动子(RIP),构建了在胰岛β细胞中过表达Pref-1/hFc的转基因小鼠品系。与野生型同窝小鼠相比,这些转基因小鼠的胰岛质量增加,胰腺中较大胰岛的比例更高。这与Pref-1基因敲除小鼠的胰腺情况相反,后者较小胰岛的比例更高。RIP-Pref-1/hFc转基因小鼠胰岛的胰岛素表达和胰岛素分泌也有所增加。因此,RIP-Pref-1/hFc转基因小鼠在空腹和进食条件下的血糖水平均正常,但血浆胰岛素水平较高。这些小鼠的葡萄糖耐量得到改善。综上所述,我们得出结论,Pref-1是胰岛β细胞和胰岛素产生的正向调节因子。