内网

检测到您当前使用浏览器版本过于老旧,会导致无法正常浏览网站;请您使用电脑里的其他浏览器如:360、QQ、搜狗浏览器的极速模式浏览,或者使用谷歌、火狐等浏览器。

下载Firefox

Identifying Mechanisms of Beta Cell Dysfunction in Diabetes by Combining Experimental and Computational Biology

日期: 2023-02-08

金沙威尼斯欢乐娱人城定量生物学中心

学术报告 

题    目: Identifying Mechanisms of Beta Cell Dysfunction in Diabetes by Combining Experimental and Computational Biology

报告人: Gaowei Wang, Ph.D.

Postdoctoral researcher in the School of Medicine at the University of California San Diego

时    间: 2月13日(周一)13:00-14:00

地    点: ZOOM线上报告

Meeting ID: 910 9636 7823

Password: cqbcqb

https://zoom.us/j/91096367823?pwd=M3d0bXIrOThoS2o4Y3dNV2JYVnUvUT09

主持人: 林杰 研究员

摘 要:

Altered function and gene regulation in pancreatic islet beta cells is a hallmark of type 2 diabetes (T2D), but we currently lack a comprehensive understanding of the mechanisms that drive beta cell dysfunction. In this talk, I will introduce a strategy to identify mechanisms of beta cell dysfunction in T2D that combines experiments and computations. I will first introduce experimental data from measurements of chromatin activity, gene expression, and cell function in single beta cells.  Then, I will introduce a machine-learning pipeline, inspired by the fluctuation test established by Luria and Delbrück, that robustly identified two T2D-relevant beta cell subtypes from heterogeneous human single-cell data. Through gene regulatory network analysis, I further identified gene regulatory programs maintaining beta cell subtype identity and determining T2D-associated functional changes in both beta cell subtypes. This study demonstrates the power of combining experimental and computational tools for identifying mechanisms of complex diseases.

报告人简介:

Gaowei Wang is currently a postdoctoral researcher in the School of Medicine at the University of California San Diego, where he studies mechanisms of beta cell dysfunction in type 2 diabetes. He received his Ph.D. in Biophysics from Shanghai Jiao Tong University, where he used methods and concepts from nonlinear dynamical systems to understand cell fate determinations.