Inceptor regulates insulin homeostasis: A new approach for diabetes therapies
- Date:
- November 25, 2024
- Source:
- Helmholtz Munich
- Summary:
- In 2021, a research team discovered the insulin-inhibitory receptor 'Inceptor' and its role as a suppressor of the insulin signaling pathway. Now, the researchers have unlocked another, even more significant function of the receptor: it binds insulin and directs its breakdown within beta cells. This discovery could lead to new therapeutic approaches that not only strengthen beta cell function but also enable a causal treatment for diabetes.
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In 2021, a research team led by Prof. Heiko Lickert from Helmholtz Munich discovered the insulin-inhibitory receptor "Inceptor" and its role as a suppressor of the insulin signaling pathway. Now, the researchers have unlocked another, even more significant function of the receptor: it binds insulin and directs its breakdown within beta cells. This discovery could lead to new therapeutic approaches that not only strengthen beta cell function but also enable a causal treatment for diabetes.
Prof. Heiko Lickert is the director of the Institute of Diabetes and Regeneration Research at Helmholtz Munich, professor at the Technical University of Munich (TUM), and member of the German Center for Diabetes Research (DZD). Together with his team, they discovered Inceptor in 2021 and described its role as an inhibitor of the insulin signaling pathway. Both Inceptor and the insulin receptor are located on the surface of beta cells, where Inceptor can block the insulin receptor, thus reducing the cells' insulin sensitivity and weakening the signaling pathway. The current study goes further, showing that Inceptor binds excess insulin within the beta cell and directs it towards degradation. "This knowledge about Inceptor's function gives us a deeper understanding of how beta cells regulate their insulin homeostasis," says Heiko Lickert.
Regeneration of Damaged Beta Cells
The increased presence of Inceptor in beta cells suggests that the receptor plays a role in insulin secretion, which is regulated by beta cells. This process is often impaired in diabetes, leading to elevated blood sugar levels. By blocking Inceptor, the researchers were able to refill beta cells' insulin stores, enhance insulin release, and prevent beta cell death. "Especially in already damaged cells, blocking Inceptor could help boost insulin production and protect the beta cells," explains Lickert.
Hope for People with Type 2 Diabetes
The findings suggest that specifically targeting Inceptor could be a promising strategy for improving the function of insulin-producing cells in people with diabetes. "Our goal is to develop new medications that support the cells' insulin balance and prolong their viability, based on our discovery"" says Lickert. Such a therapy could especially help individuals in the early stages of type 2 diabetes to slow disease progression and reduce the risk of complications.
From Lab to Practice: A Start-up for New Diabetes Therapies
To translate these findings from the lab to real-world applications, Lickert has founded a start-up. The company is working on developing drugs that specifically block Inceptor to protect or regenerate beta cells. Preclinical studies are initially needed to test the safety and efficacy of these new therapeutic approaches. "Our goal is to pave the way for clinical trials and thereby contribute to the treatment, and hopefully even the cure, of diabetes," says Lickert.
Story Source:
Materials provided by Helmholtz Munich. Note: Content may be edited for style and length.
Journal Reference:
- Johanna Siehler, Sara Bilekova, Prisca Chapouton, Alessandro Dema, Pascal Albanese, Sem Tamara, Chirag Jain, Michael Sterr, Stephen J. Enos, Chunguang Chen, Chetna Malhotra, Adrian Villalba, Leopold Schomann, Sreya Bhattacharya, Jin Feng, Melis Akgün Canan, Federico Ribaudo, Ansarullah, Ingo Burtscher, Christin Ahlbrecht, Oliver Plettenburg, Thomas Kurth, Raphael Scharfmann, Stephan Speier, Richard A. Scheltema, Heiko Lickert. Inceptor binds to and directs insulin towards lysosomal degradation in β cells. Nature Metabolism, 2024; DOI: 10.1038/s42255-024-01164-y
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