Imperial College London
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DrJorgeBernardino de la Serna

Faculty of Medicine, National Heart & Lung Institute

Senior Lecturer in Inhalation Toxicology and Pharmacology
 
 
 
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Contact

 

+44 (0)20 7594 3277j.bernardino-de-la-serna Website

 
 
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Location

 

CubicleSir Alexander Fleming BuildingSouth Kensington Campus

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Summary

 

Publications

Citation

BibTex format

@article{Manchanda:2023:endocr/bqad028,
author = {Manchanda, Y and Bitsi, S and Chen, S and Broichhagen, J and Bernardino, de la Serna J and Jones, B and Tomas, A},
doi = {endocr/bqad028},
journal = {Endocrinology},
pages = {1--15},
title = {Enhanced endosomal signaling and desensitization of GLP-1R versus GIPR in pancreatic beta cells},
url = {http://dx.doi.org/10.1210/endocr/bqad028},
volume = {164},
year = {2023}
}
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RIS format (EndNote, RefMan)

TY  - JOUR
AB  - The incretin receptors, glucagon-like peptide-1 receptor (GLP-1R) and glucose-dependent insulinotropic polypeptide receptor (GIPR), are prime therapeutic targets for the treatment of type 2 diabetes (T2D) and obesity. They are expressed in pancreatic beta cells where they potentiate insulin release in response to food intake. Despite GIP being the main incretin in healthy individuals, GLP-1R has been favored as a therapeutic target due to blunted GIPR responses in T2D patients and conflicting effects of GIPR agonists and antagonists in improving glucose tolerance and preventing weight gain. There is, however, a recently renewed interest in GIPR biology following the realization that GIPR responses can be restored after an initial period of blood glucose normalization and the recent development of dual GLP-1R/GIPR agonists with superior capacity for controlling blood glucose levels and weight. The importance of GLP-1R trafficking and subcellular signaling in the control of receptor outputs is well established, but little is known about the pattern of spatiotemporal signaling from the GIPR in beta cells. Here, we have directly compared surface expression, trafficking and signaling characteristics of both incretin receptors in pancreatic beta cells to identify potential differences that might underlie distinct pharmacological responses associated with each receptor. Our results indicate increased cell surface levels, internalization, degradation, and endosomal versus plasma membrane activity for the GLP-1R, while the GIPR is instead associated with increased plasma membrane recycling, reduced desensitization, and enhanced downstream signal amplification. These differences might have potential implications for the capacity of each incretin receptor to control beta cell function.
AU  - Manchanda,Y
AU  - Bitsi,S
AU  - Chen,S
AU  - Broichhagen,J
AU  - Bernardino,de la Serna J
AU  - Jones,B
AU  - Tomas,A
DO  - endocr/bqad028
EP  - 15
PY  - 2023///
SN  - 0013-7227
SP  - 1
TI  - Enhanced endosomal signaling and desensitization of GLP-1R versus GIPR in pancreatic beta cells
T2  - Endocrinology
UR  - http://dx.doi.org/10.1210/endocr/bqad028
UR  - https://www.ncbi.nlm.nih.gov/pubmed/36774542
UR  - https://academic.oup.com/endo/article/164/5/bqad028/7034684?login=true
UR  - http://hdl.handle.net/10044/1/102944
VL  - 164
ER  -
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