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The effect of the small-molecule luteinising hormone receptor agonist, LHR-Chap, on receptor trafficking and G protein-independent signalling.

Dissertation (MSc (Human Physiology))--University of Pretoria, 2022.

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Other Authors: Newton, Claire
Format: Thesis
Language:English
Published: University of Pretoria 2022
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_version_ 1867613528049844224
access_status_str Open Access
author2 Newton, Claire
author_browse Newton, Claire
author_facet Newton, Claire
collection Thesis
dc_rights_str_mv © 2022 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Dissertation (MSc (Human Physiology))--University of Pretoria, 2022.
format Thesis
id oai:repository.up.ac.za:2263/86177
institution University of Pretoria (South Africa)
language English
last_indexed 2026-06-10T12:37:34.574Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2022
publishDateRange 2022
publishDateSort 2022
publisher University of Pretoria
publisherStr University of Pretoria
record_format dspace
source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/86177 The effect of the small-molecule luteinising hormone receptor agonist, LHR-Chap, on receptor trafficking and G protein-independent signalling. Newton, Claire u16254512@tuks.co.za van den Bout, Iman Vermaak, Monique UCTD LHR-Chap G protein-coupled receptors Luteinising hormone receptor G protein signalling Receptor trafficking Dissertation (MSc (Human Physiology))--University of Pretoria, 2022. Sexual development and reproductive function are controlled by the hypothalamic-pituitary-gonadal axis which regulates secretion of luteinising hormone (LH) and follicle stimulating hormone (FSH) which travel through the circulation to the gonads where they bind to their respective receptors, the luteinising hormone receptor (LHR) and follicle stimulating hormone (FSHR). The LHR forms part of the G protein-coupled receptor (GPCR) superfamily. Upon ligand binding, GPCRs undergo a conformational change enabling them to couple to specific families of intracellular heterotrimeric G proteins. Activation of G protein-dependent signalling pathways has been shown to stimulate the mitogen activation protein kinase signalling (MAPK) cascade. Interestingly, signalling through GPCRs also occurs in a G protein-independent manner. Typically, this is mediated by β-arrestin binding to the receptor which are also involved in the regulatory processes of GPCR desensitisation, internalisation and downregulation. Gonadotropins have been used extensively in assisted reproductive therapies. The focus of several drug discovery efforts has been to develop non-peptide analogues for these hormones in order to improve convenience of treatment and production. One such compound, LHR-Chap, shows great therapeutic potential. However, not much is known about the signalling mechanisms activated in response to this compound. Therefore, the aim of the present study was to examine the effects of LHR-Chap on LHR induced signalling pathways and trafficking. The data demonstrated biased agonism of LHR-Chap, as it was shown that, while the native cognate hormone activated the cAMP signalling pathway, the IP3 signalling pathway and the ERK/MAPK signalling pathway, LHR-Chap only stimulated the cAMP signalling pathway. Furthermore, evidence of differential LHR trafficking in response to treatment with native hormone vs LHR-Chap was also observed. These findings highlight the importance of further studies relating to LHR signalling/trafficking in response to LHR-Chap. Physiology MSc (Human Physiology) Unrestricted 2022-07-14T11:22:45Z 2022-07-14T11:22:45Z 2022 2022 Dissertation * S2022 https://repository.up.ac.za/handle/2263/86177 en © 2022 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle UCTD
LHR-Chap
G protein-coupled receptors
Luteinising hormone receptor
G protein signalling
Receptor trafficking
The effect of the small-molecule luteinising hormone receptor agonist, LHR-Chap, on receptor trafficking and G protein-independent signalling.
title The effect of the small-molecule luteinising hormone receptor agonist, LHR-Chap, on receptor trafficking and G protein-independent signalling.
title_full The effect of the small-molecule luteinising hormone receptor agonist, LHR-Chap, on receptor trafficking and G protein-independent signalling.
title_fullStr The effect of the small-molecule luteinising hormone receptor agonist, LHR-Chap, on receptor trafficking and G protein-independent signalling.
title_full_unstemmed The effect of the small-molecule luteinising hormone receptor agonist, LHR-Chap, on receptor trafficking and G protein-independent signalling.
title_short The effect of the small-molecule luteinising hormone receptor agonist, LHR-Chap, on receptor trafficking and G protein-independent signalling.
title_sort effect of the small molecule luteinising hormone receptor agonist lhr chap on receptor trafficking and g protein independent signalling
topic UCTD
LHR-Chap
G protein-coupled receptors
Luteinising hormone receptor
G protein signalling
Receptor trafficking
url https://repository.up.ac.za/handle/2263/86177