来源于IGF-II的Vesiculin在糖尿病前期小鼠模型中驱动胰岛细胞质量增加。

IF 1.9 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Islets Pub Date : 2022-01-01 DOI:10.1080/19382014.2021.1982326
Kate L Lee, Jacqueline F Aitken, Xun Li, Kirsten Montgomery, Huai-L Hsu, Geoffrey M Williams, Margaret A Brimble, Garth J S Cooper
{"title":"来源于IGF-II的Vesiculin在糖尿病前期小鼠模型中驱动胰岛细胞质量增加。","authors":"Kate L Lee,&nbsp;Jacqueline F Aitken,&nbsp;Xun Li,&nbsp;Kirsten Montgomery,&nbsp;Huai-L Hsu,&nbsp;Geoffrey M Williams,&nbsp;Margaret A Brimble,&nbsp;Garth J S Cooper","doi":"10.1080/19382014.2021.1982326","DOIUrl":null,"url":null,"abstract":"<p><p>Pancreatic islet-cell function and volume are both key determinants of the maintenance of metabolic health. Insulin resistance and islet-cell dysfunction often occur in the earlier stages of type 2 diabetes (T2D) progression. The ability of the islet cells to respond to insulin resistance by increasing hormone output accompanied by increased islet-cell volume is key to maintaining blood glucose control and preventing further disease progression. Eventual β-cell loss is the main driver of full-blown T2D and insulin-dependency. Researchers are targeting T2D with approaches that include those aimed at enhancing the function of the patient's existing β-cell population, or replacing islet β-cells. Another approach is to look for agents that enhance the natural capacity of the β-cell population to expand. Here we aimed to study the effects of a new putative β-cell growth factor on a mouse model of pre-diabetes. We asked whether: 1) 4-week's treatment with vesiculin, a two-chain peptide derived by processing from IGF-II, had any measurable effect on pre-diabetic mice vs vehicle; and 2) whether the effects were the same in non-diabetic littermate controls. Although treatment with vesiculin did not alter blood glucose levels over this time period, there was a doubling of the Proliferating Cell Nuclear Antigen (PCNA) detectable in the islets of treated pre-diabetic but not control mice and this was accompanied by increased insulin- and glucagon-positive stained areas in the pancreatic islets.</p>","PeriodicalId":14671,"journal":{"name":"Islets","volume":"14 1","pages":"14-22"},"PeriodicalIF":1.9000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/33/83/KISL_14_1982326.PMC8632304.pdf","citationCount":"0","resultStr":"{\"title\":\"Vesiculin derived from IGF-II drives increased islet cell mass in a mouse model of pre-diabetes.\",\"authors\":\"Kate L Lee,&nbsp;Jacqueline F Aitken,&nbsp;Xun Li,&nbsp;Kirsten Montgomery,&nbsp;Huai-L Hsu,&nbsp;Geoffrey M Williams,&nbsp;Margaret A Brimble,&nbsp;Garth J S Cooper\",\"doi\":\"10.1080/19382014.2021.1982326\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Pancreatic islet-cell function and volume are both key determinants of the maintenance of metabolic health. Insulin resistance and islet-cell dysfunction often occur in the earlier stages of type 2 diabetes (T2D) progression. The ability of the islet cells to respond to insulin resistance by increasing hormone output accompanied by increased islet-cell volume is key to maintaining blood glucose control and preventing further disease progression. Eventual β-cell loss is the main driver of full-blown T2D and insulin-dependency. Researchers are targeting T2D with approaches that include those aimed at enhancing the function of the patient's existing β-cell population, or replacing islet β-cells. Another approach is to look for agents that enhance the natural capacity of the β-cell population to expand. Here we aimed to study the effects of a new putative β-cell growth factor on a mouse model of pre-diabetes. We asked whether: 1) 4-week's treatment with vesiculin, a two-chain peptide derived by processing from IGF-II, had any measurable effect on pre-diabetic mice vs vehicle; and 2) whether the effects were the same in non-diabetic littermate controls. Although treatment with vesiculin did not alter blood glucose levels over this time period, there was a doubling of the Proliferating Cell Nuclear Antigen (PCNA) detectable in the islets of treated pre-diabetic but not control mice and this was accompanied by increased insulin- and glucagon-positive stained areas in the pancreatic islets.</p>\",\"PeriodicalId\":14671,\"journal\":{\"name\":\"Islets\",\"volume\":\"14 1\",\"pages\":\"14-22\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/33/83/KISL_14_1982326.PMC8632304.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Islets\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/19382014.2021.1982326\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Islets","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/19382014.2021.1982326","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0

摘要

胰岛细胞的功能和体积都是维持代谢健康的关键决定因素。胰岛素抵抗和胰岛细胞功能障碍常发生在2型糖尿病(T2D)进展的早期阶段。胰岛细胞通过增加激素输出并增加胰岛细胞体积来应对胰岛素抵抗的能力是维持血糖控制和防止进一步疾病进展的关键。最终的β细胞损失是t2dm和胰岛素依赖的主要驱动因素。研究人员针对T2D的治疗方法包括增强患者现有β细胞群的功能,或替代胰岛β细胞。另一种方法是寻找能够增强β细胞群体自然扩张能力的药物。本研究旨在研究一种新的β细胞生长因子对糖尿病前期小鼠模型的影响。我们的问题是:1)用vesiculin(一种由IGF-II加工而成的双链肽)治疗4周后,对糖尿病前期小鼠与对照组是否有可测量的影响;2)在非糖尿病的同窝鼠中是否同样有效。尽管在这段时间内用维囊素治疗并没有改变血糖水平,但在治疗的糖尿病前期小鼠的胰岛中检测到的增殖细胞核抗原(PCNA)增加了一倍,而对照组小鼠则没有,这伴随着胰岛中胰岛素和胰高血糖素阳性染色区域的增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

摘要图片

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
Vesiculin derived from IGF-II drives increased islet cell mass in a mouse model of pre-diabetes.

Pancreatic islet-cell function and volume are both key determinants of the maintenance of metabolic health. Insulin resistance and islet-cell dysfunction often occur in the earlier stages of type 2 diabetes (T2D) progression. The ability of the islet cells to respond to insulin resistance by increasing hormone output accompanied by increased islet-cell volume is key to maintaining blood glucose control and preventing further disease progression. Eventual β-cell loss is the main driver of full-blown T2D and insulin-dependency. Researchers are targeting T2D with approaches that include those aimed at enhancing the function of the patient's existing β-cell population, or replacing islet β-cells. Another approach is to look for agents that enhance the natural capacity of the β-cell population to expand. Here we aimed to study the effects of a new putative β-cell growth factor on a mouse model of pre-diabetes. We asked whether: 1) 4-week's treatment with vesiculin, a two-chain peptide derived by processing from IGF-II, had any measurable effect on pre-diabetic mice vs vehicle; and 2) whether the effects were the same in non-diabetic littermate controls. Although treatment with vesiculin did not alter blood glucose levels over this time period, there was a doubling of the Proliferating Cell Nuclear Antigen (PCNA) detectable in the islets of treated pre-diabetic but not control mice and this was accompanied by increased insulin- and glucagon-positive stained areas in the pancreatic islets.

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
Islets
Islets ENDOCRINOLOGY & METABOLISM-
CiteScore
3.30
自引率
4.50%
发文量
10
审稿时长
>12 weeks
期刊介绍: Islets is the first international, peer-reviewed research journal dedicated to islet biology. Islets publishes high-quality clinical and experimental research into the physiology and pathology of the islets of Langerhans. In addition to original research manuscripts, Islets is the leading source for cutting-edge Perspectives, Reviews and Commentaries. Our goal is to foster communication and a rapid exchange of information through timely publication of important results using print as well as electronic formats.
期刊最新文献
3D evaluation of the extracellular matrix of hypoxic pancreatic islets using light sheet fluorescence microscopy. Serum from pregnant donors induces human beta cell proliferation. Characterizing the effects of Dechlorane Plus on β-cells: a comparative study across models and species. Decreased islet amyloid polypeptide staining in the islets of insulinoma patients. Human research islet cell culture outcomes at the Alberta Diabetes Institute IsletCore.
×
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