American Diabetes Association
8 files

Generation and characterization of a novel mouse model that allows spatiotemporal quantification of pancreatic β-cell proliferation

posted on 2020-08-07, 16:41 authored by Ada AdminAda Admin, Shinsuke Tokumoto, Daisuke Yabe, Hisato Tatsuoka, Ryota Usui, Muhammad Fauzi, Ainur Botagarova, Hisanori Goto, Pedro Luis Herrera, Masahito Ogura, Nobuya Inagaki
Pancreatic β-cell proliferation has been gaining much attention as a therapeutic target for prevention and treatment of diabetes. In order to evaluate potential β-cell mitogens, accurate and reliable methods for detection and quantification of the β-cell proliferation rate are indispensable. In this study, we developed a novel tool that specifically labels replicating β cells as mVenus+ cells by using RIP-Cre;R26Fucci2aR mice expressing the fluorescent ubiquitination-based cell cycle indicator Fucci2a in β cells. In response to β-cell proliferation stimuli such as insulin receptor antagonist S961 and diet-induced obesity (DIO), the number of EdU+ insulin+ cells per insulin+ cells and the number of mVenus+ cells per mCherry+ mVenus- cells + mCherry- mVenus+ cells were similarly increased in these mice. Three-dimensional imaging of optically cleared pancreas tissue from these mice enabled quantification of replicating β cells in the islets and morphometric analysis of the islets following known mitogenic interventions such as S961, DIO, pregnancy and partial pancreatectomy. Thus, this novel mouse line is a powerful tool for spatiotemporal analysis and quantification of β-cell proliferation in response to mitogenic stimulation.


This work was supported by grants from Japan Society for the Promotion of Sciences (KAKENHI Grant Number: 26111004, 17K09825 and 17K19654). This work was also supported by Kyoto University Live Imaging Center and in part by Grants-in-Aid KAKENHI 16H06280 “ABiS”


Usage metrics



    Ref. manager