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Mathematical modelling of glycolysis in differentiated mouse adipocytes 3T3-L1

Thesis (MSc)--Stellenbosch University, 2021.

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Main Author: De Villiers, William
Other Authors: Snoep, Jacob Leendert
Format: Thesis
Language:en_ZA
Published: Stellenbosch : Stellenbosch University 2021
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access_status_str Open Access
author De Villiers, William
author2 Snoep, Jacob Leendert
author_browse De Villiers, William
Snoep, Jacob Leendert
author_facet Snoep, Jacob Leendert
De Villiers, William
author_sort De Villiers, William
collection Thesis
description Thesis (MSc)--Stellenbosch University, 2021.
format Thesis
id oai:scholar.sun.ac.za:10019.1/110283
institution Stellenbosch University (South Africa)
language en_ZA
last_indexed 2026-06-10T12:41:10.692Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from SUNScholar — Stellenbosch University Repository
publishDate 2021
publishDateRange 2021
publishDateSort 2021
publisher Stellenbosch : Stellenbosch University
publisherStr Stellenbosch : Stellenbosch University
record_format dspace
source_str SUNScholar — Stellenbosch University Repository
spelling oai:scholar.sun.ac.za:10019.1/110283 Mathematical modelling of glycolysis in differentiated mouse adipocytes 3T3-L1 De Villiers, William Snoep, Jacob Leendert Van Niekerk, David Douglas Stellenbosch University. Faculty of Science. Dept. of Biochemistry. Glycolysis -- Mathematical models Triacylglycerols Adipocytes Diabetes -- Animal models Diabetes mellitus UCTD Thesis (MSc)--Stellenbosch University, 2021. ENGLISH ABSTRACT: Diabetes mellitus is a metabolic disease characterised by high blood sugar levels, primarily caused by insulin resistance and the resulting inability of the body to process glucose. Any tissue or cell that utilizes glucose is a target of diabetes research. Obesity is closely related to the development of diabetes due to the swelling of adipocytes caused by triacylglycerol formation. As glucose and its breakdown by glycolysis are directly responsible for supplying triacylglycerol formation, the focus of this work was on glycolysis in 3T3-L1 adipocytes. A bottom-up modelling approach was used in which all enzymes within glycolysis and the initial lipogenic enzyme G3PDH were characterised in order to create a kinetic model for glycolysis in 3T3-L1 adipocytes. Nondiabetic adipocyte cell extracts were utilized due to the need for a reference state model. Validation was performed using an HPLC analysis of glycolytic intermediates and co-factors. The validation was partially successful with glucose consumption and several glycolytic intermediate dynamics well described. Lactate production was underestimated in the model due to the high G3PDH activity within cell extracts which caused a signi cant fraction of the glucose to be converted via the glycerol branch, which was not seen to the same degree in the HPLC analysis. Being the rst model of its kind to be constructed for adipocytes, this work has laid the groundwork for further modelling of adipocyte glucose metabolism to better understand the diabetic condition in adipose tissue. AFRIKAANSE OPSOMMING: Diabetes mellitus is 'n metaboliese siekte wat gekenmerk word deur hoë bloedsuikervlakke, hoofsaaklik veroorsaak deur insulienweerstandigheid en die gevolglike onvermoë van die liggaam om glukose te verwerk. Enige weefsel of sel wat glukose gebruik, is 'n teiken vir navorsing oor diabetes. Vetsug hou nou verband met die ontwikkeling van diabetes as gevolg van die swelling van adiposiete wat veroorsaak word deur die vorming van triasielgliserol. Aangesien glukose en die afbreek daarvan deur glikolise direk verantwoordelik is vir die verska ng van triasielgliserolvorming, was die fokus van hierdie werk op glikolise in 3T3-L1-adiposiete. 'n Benaderingsmodel benadering is gebruik waarin alle ensieme binne glikolise en die aanvanklike lipogene ensiem G3PDH gekarakteriseer is om 'n kinetiese model vir glikolise in 3T3-L1 adiposiete te skep. Nie-diabetiese adiposiet selekstrakte is gebruik as gevolg van die behoefte aan 'n verwysingstoestandmodel. Validasie is uitgevoer met behulp van 'n HPLC-analise van glikolitiese tussenprodukte en medefaktore. Die validering was gedeeltelik suksesvol met glukoseverbruik en verskeie glikolitiese intermedi êre dinamika wat goed beskryf is. Laktaatproduksie is in die model onderskat as gevolg van die hoë G3PDH-aktiwiteit in selekstrakte, wat veroorsaak het dat 'n beduidende fraksie van die glukose via die gliserolvertakking omgeskakel is, wat nie in dieselfde mate in die HPLC-analise gesien is nie. Aangesien dit die eerste model in sy soort is wat vir adiposiete vervaardig is, het dit die basis gelê vir verdere modellering van metabolisme van adiposiete glukose om die diabetiese toestand in vetweefsel beter te verstaan. Masters 2021-03-02T09:26:33Z 2021-04-22T10:12:26Z 2021-09-02T03:00:07Z 2021-03 Thesis http://hdl.handle.net/10019.1/110283 en_ZA v, 93 pages application/pdf Stellenbosch : Stellenbosch University Stellenbosch : Stellenbosch University
spellingShingle Glycolysis -- Mathematical models
Triacylglycerols
Adipocytes
Diabetes -- Animal models
Diabetes mellitus
UCTD
De Villiers, William
Mathematical modelling of glycolysis in differentiated mouse adipocytes 3T3-L1
title Mathematical modelling of glycolysis in differentiated mouse adipocytes 3T3-L1
title_full Mathematical modelling of glycolysis in differentiated mouse adipocytes 3T3-L1
title_fullStr Mathematical modelling of glycolysis in differentiated mouse adipocytes 3T3-L1
title_full_unstemmed Mathematical modelling of glycolysis in differentiated mouse adipocytes 3T3-L1
title_short Mathematical modelling of glycolysis in differentiated mouse adipocytes 3T3-L1
title_sort mathematical modelling of glycolysis in differentiated mouse adipocytes 3t3 l1
topic Glycolysis -- Mathematical models
Triacylglycerols
Adipocytes
Diabetes -- Animal models
Diabetes mellitus
UCTD
url http://hdl.handle.net/10019.1/110283
work_keys_str_mv AT devillierswilliam mathematicalmodellingofglycolysisindifferentiatedmouseadipocytes3t3l1