Review: pancreatic beta-cell neogenesis revisited.

Maryline Paris, Cécile Tourrel-Cuzin, Cédric Plachot, Alain Ktorza
{"title":"Review: pancreatic beta-cell neogenesis revisited.","authors":"Maryline Paris,&nbsp;Cécile Tourrel-Cuzin,&nbsp;Cédric Plachot,&nbsp;Alain Ktorza","doi":"10.1080/15438600490455079","DOIUrl":null,"url":null,"abstract":"<p><p>Beta-cell neogenesis triggers the generation of new beta-cells from precursor cells. Neogenesis from duct epithelium is the most currently described and the best documented process of differentiation of precursor cells into beta-cells. It is contributes not only to beta-cell mass expansion during fetal and nonatal life but it is also involved in the maintenance of the beta-cell mass in adults. It is also required for the increase in beta-cell mass in situations of increase insulin demand (obesity, pregnancy). A large number of factors controlling the differentiation of beta-cells has been identified. They are classified into the following main categories: growth factors, cytokine and inflammatory factors, and hormones such as PTHrP and GLP-1. The fact that intestinal incretin hormone GLP-1 exerts a major trophic role on pancreatic beta-cells provides insights into the possibility to pharmacologically stimulate beta-cell neogenesis. This could have important implications for the of treatment of type 1 and type 2 diabetes. Transdifferentiation, that is, the differentiation of already differentiated cells into beta-cells, remains controversial. However, more and more studies support this concept. The cells, which can potentially \"transdifferentiate\" into beta-cells, can belong to the pancreas (acinar cells) and even islets, or originate from extra-pancreatic tissues such as the liver. Neogenesis from intra-islet precursors also have been proposed and subpopulations of cell precursors inside islets have been described by some authors. Nestin positive cells, which have been considered as the main candidates, appear rather as progenitors of endothelial cells rather than beta-cells and contribute to angiogenesis rather than neogenesis. To take advantage of the different differentiation processes may be a direction for future cellular therapies. Ultimately, a better understanding of the molecular mechanisms involved in beta-cell neogenesis will allow us to use any type of differentiated and/or undifferentiated cells as a source of potential cell precursors.</p>","PeriodicalId":86960,"journal":{"name":"Experimental diabesity research","volume":"5 2","pages":"111-21"},"PeriodicalIF":0.0000,"publicationDate":"2004-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15438600490455079","citationCount":"46","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental diabesity research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/15438600490455079","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 46

Abstract

Beta-cell neogenesis triggers the generation of new beta-cells from precursor cells. Neogenesis from duct epithelium is the most currently described and the best documented process of differentiation of precursor cells into beta-cells. It is contributes not only to beta-cell mass expansion during fetal and nonatal life but it is also involved in the maintenance of the beta-cell mass in adults. It is also required for the increase in beta-cell mass in situations of increase insulin demand (obesity, pregnancy). A large number of factors controlling the differentiation of beta-cells has been identified. They are classified into the following main categories: growth factors, cytokine and inflammatory factors, and hormones such as PTHrP and GLP-1. The fact that intestinal incretin hormone GLP-1 exerts a major trophic role on pancreatic beta-cells provides insights into the possibility to pharmacologically stimulate beta-cell neogenesis. This could have important implications for the of treatment of type 1 and type 2 diabetes. Transdifferentiation, that is, the differentiation of already differentiated cells into beta-cells, remains controversial. However, more and more studies support this concept. The cells, which can potentially "transdifferentiate" into beta-cells, can belong to the pancreas (acinar cells) and even islets, or originate from extra-pancreatic tissues such as the liver. Neogenesis from intra-islet precursors also have been proposed and subpopulations of cell precursors inside islets have been described by some authors. Nestin positive cells, which have been considered as the main candidates, appear rather as progenitors of endothelial cells rather than beta-cells and contribute to angiogenesis rather than neogenesis. To take advantage of the different differentiation processes may be a direction for future cellular therapies. Ultimately, a better understanding of the molecular mechanisms involved in beta-cell neogenesis will allow us to use any type of differentiated and/or undifferentiated cells as a source of potential cell precursors.

回顾:胰腺β细胞新生的重新审视。
β细胞新生触发前体细胞产生新的β细胞。导管上皮的新生是目前描述最多、记录最充分的前体细胞向β细胞分化的过程。它不仅有助于胎儿和胎儿期β细胞质量的扩增,而且还参与成人β细胞质量的维持。在胰岛素需求增加的情况下(肥胖、怀孕),β细胞质量的增加也是必需的。大量控制β细胞分化的因素已被确定。它们主要分为以下几类:生长因子,细胞因子和炎症因子,激素如PTHrP和GLP-1。肠促胰岛素激素GLP-1对胰腺β细胞发挥重要的营养作用,这一事实为药理学刺激β细胞新生的可能性提供了新的见解。这可能对1型和2型糖尿病的治疗有重要意义。转分化,即已经分化的细胞向β细胞的分化,仍然存在争议。然而,越来越多的研究支持这一观点。这些细胞有可能“转分化”为β细胞,它们可能属于胰腺(腺泡细胞)甚至胰岛,也可能来自胰腺外组织,如肝脏。一些作者也提出了胰岛内前体的新生,并描述了胰岛内细胞前体的亚群。Nestin阳性细胞被认为是主要的候选细胞,它们更像是内皮细胞而不是β细胞的祖细胞,并有助于血管生成而不是新生。利用不同的分化过程可能是未来细胞治疗的一个方向。最终,更好地理解β细胞新生的分子机制将使我们能够使用任何类型的分化和/或未分化细胞作为潜在细胞前体的来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信