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Heterogeneous development of beta-cell populations in diabetes-resistant and -susceptible mice

Date:
August 31, 2022
Source:
Deutsches Zentrum fuer Diabetesforschung DZD
Summary:
Progressive dysfunction and failure of insulin-releasing beta-cells is a hallmark of type 2 diabetes (T2D). Researchers have now shown that diabetes-resistant and -susceptible mice respond differently to a carbohydrate-rich diet. The gene expression of the beta cells of the diabetes-resistant mice changed in such a way that a protective beta cell cluster developed. In diabetic-prone mice, a failure to adjust gene expression in response to rising blood glucose levels led to increased metabolic stress and beta cell failure.
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Progressive dysfunction and failure of insulin-releasing β-cells is a hallmark of type 2 diabetes (T2D). DZD researchers have now shown that diabetes resistant and -susceptible mice respond differently to a carbohydrate-rich diet. The gene expression of the beta cells of the diabetes-resistant mice changed in such a way that a protective beta cell cluster developed. In diabetic-prone mice, a failure to adjust gene expression in response to rising blood glucose levels led to increased metabolic stress and beta cell failure. The study was published in the journal Diabetes.

To investigate the mechanisms of beta cell loss in T2D, researchers at the DZD performed single-cell RNA sequencing of islets of Langerhans in two obese mouse strains that differ in their susceptibility to diabetes. Both the diabetes-prone and diabetes-resistant mice have six different groups of beta cells in their islets, which are very similar in abundance before treatment. However, after feeding a carbohydrate-rich diabetogenic diet for two days, the composition of the beta cell clusters differed significantly between the strains. The islet cells of the diabetes-resistant mice developed into a protective beta cell cluster (Beta4). This protective cluster showed indications of reduced beta cell identity (such as downregulation of the GLUT2, GLP1R and MafA genes). Characteristics of mature beta-cell expression decreased. This likely leads to lower glucose uptake and for some, even gain of the ability to divide to ultimately produce more beta cells. An in vitro knockdown of GLUT2 in beta cells led to reduced stress reactions and a decrease in apoptosis markers (apoptosis = programmed cell death). This could explain the improved survival of beta cells in diabetes-resistant mice.

In contrast, beta cells from diabetic-prone mice responded with expression changes indicative of metabolic pressure and stress in the endoplasmic reticulum. They also lacked the adaptation of gene expression towards a more dedifferentiated state. This can presumably contribute to a later loss of beta cells, which in turn contributes to the development of diabetes.

"Our study provides new clues as to why obesity does not always lead to type 2 diabetes. The ability of mice, and presumably humans as well, to respond to elevated blood glucose levels with a transient reduction in their beta cell identity appears to play a key role in protecting them from loss of function and/or apoptosis," said Annette Schürmann, lead author of the study.

About the study

Researchers from the German Center for Diabetes Research, Helmholtz Munich and the University Hospital Carl Gustav Carus and the Medical Faculty of TU Dresden were involved in the study, which was led by the German Institute of Human Nutrition Potsdam-Rehbruecke (DIfE).


Story Source:

Materials provided by Deutsches Zentrum fuer Diabetesforschung DZD. Note: Content may be edited for style and length.


Journal Reference:

  1. Pascal Gottmann, Thilo Speckmann, Mandy Stadion, Erika Zuljan, Heja Aga, Michael Sterr, Maren Büttner, Patrícia Martínez Santos, Markus Jähnert, Stefan R. Bornstein, Fabian J. Theis, Heiko Lickert, Annette Schürmann. Heterogeneous Development of β-Cell Populations in Diabetes-Resistant and -Susceptible Mice. Diabetes, 2022; 71 (9): 1962 DOI: 10.2337/db21-1030

Cite This Page:

Deutsches Zentrum fuer Diabetesforschung DZD. "Heterogeneous development of beta-cell populations in diabetes-resistant and -susceptible mice." ScienceDaily. ScienceDaily, 31 August 2022. <www.sciencedaily.com/releases/2022/08/220831095016.htm>.
Deutsches Zentrum fuer Diabetesforschung DZD. (2022, August 31). Heterogeneous development of beta-cell populations in diabetes-resistant and -susceptible mice. ScienceDaily. Retrieved June 17, 2024 from www.sciencedaily.com/releases/2022/08/220831095016.htm
Deutsches Zentrum fuer Diabetesforschung DZD. "Heterogeneous development of beta-cell populations in diabetes-resistant and -susceptible mice." ScienceDaily. www.sciencedaily.com/releases/2022/08/220831095016.htm (accessed June 17, 2024).

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