Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.797637
Title: Understanding the mechanisms regulating SCFA mediated release of anorectic gut hormones
Author: Caengprasath, Natarin
ISNI:       0000 0004 8504 6824
Awarding Body: Imperial College London
Current Institution: Imperial College London
Date of Award: 2019
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Abstract:
Obesity is a fast-growing epidemic that poses a major challenge to the public health. There is a current lack of safe and effective anti-obesity treatment options, therefore an improved treatment option is critical. Short chain fatty acids (SCFAs), produced in the colon via fermentation of non-digestible carbohydrates by gut microbiota, activates FFA2 and FFA3, G-protein coupled receptors (GPCRs) that stimulate the release of anorectic gut hormones GLP-1 and PYY. However, the underlying molecular mechanisms stimulating their release are poorly understood. A fundamental mechanism controlling the signalling capacity of GPCRs is via receptor trafficking to diverse cellular compartments such as early endosomes (EE), or very early endosomes (VEE). A subpopulation of VEEs contains the adaptor protein APPL1, essential for driving receptor recycling from the VEE and regulating endosomal G protein signalling. I therefore characterised the signalling pathways exerted by SCFAs in intestinal enteroendocrine cells and colonic organoids and elucidated the trafficking properties of FFA2 that regulate anorectic gut hormone release. In enteroendocrine cells, SCFAs are unable to elicit Gαq/11-signalling but robustly activates Gαi/o signalling which is important for propionate induced GLP-1 secretion. FFA2 undergoes both constitutive and ligand induced internalisation. Following ligand-induced internalisation, FFA2 traffics to the VEE to activate Gαi endosomal signalling that is regulated by APPL1. In addition, by employing high resolution single vesicle imaging, I unveiled propionate-induced FFA2 recycling is APPL1 dependent. I also examined the dependence of receptor internalisation and found that receptor internalisation is critical only for propionate induced- Gαi/o signalling, p38 activation and GLP-1 release, while Gαq/11 signalling occurs from the plasma membrane. Together these findings suggest an important spatial requirement for propionate-mediated activity and uncovers novel mechanisms regulating the release of anorectic gut hormone, GLP-1.
Supervisor: Frost, Gary ; Hanyaloglu, Aylin ; Tate, Edward Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.797637  DOI:
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