Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20453
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dc.contributor.authorEllis, R-
dc.contributor.authorKaterelos, Marina-
dc.contributor.authorChoy, Suet-Wan-
dc.contributor.authorCook, Natasha-
dc.contributor.authorLee, M-
dc.contributor.authorPaizis, Kathy-
dc.contributor.authorPell, G-
dc.contributor.authorWalker, S-
dc.contributor.authorPower, David A-
dc.contributor.authorMount, Peter F-
dc.date2019-
dc.date.accessioned2019-03-14T22:35:19Z-
dc.date.available2019-03-14T22:35:19Z-
dc.date.issued2019-02-28-
dc.identifier.citationJournal of Translational Medicine 2019; 17(1): 60en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20453-
dc.description.abstractGlycolysis is altered in various kidney diseases, but little is known about glycolysis in pre-eclampsia, a multi-system disorder with major pathological effects on the kidney. Urinary exosomes provide a non-invasive alternative for studying changes in kidney metabolism. This study aims to characterise the expression and phosphorylation of isozymes of the key glycolytic regulatory protein, 6-phosphofructokinase-2-kinase/fructose-2,6-bisphosphatase (PFK-2/FBPase-2), in urinary exosomes of subjects with pre-eclampsia (PE), compared to normotensive non-pregnant (NC) and normotensive pregnant (NP) controls. A cross-sectional study of NC (n = 19), NP (n = 23) and PE (n = 29) subjects was performed. Exosomes were isolated from urine samples by differential ultracentrifugation, and then analyzed by Western blot and densitometry for expression of PFK-2/FBPase-2 isozymes (PFKFB2, PFKFB3 and PFKFB4) and phosphorylation of PFKFB2 at residues Ser483 and Ser466 and PFKFB3 at Ser461. PFKFB2 expression was increased 4.7-fold in PE compared to NP (p < 0.001). PFKFB2 phosphorylation at Ser483 was increased 2.6-fold in PE compared to NP (p = 0.002). Expression of phosphorylated PFKFB2/PFKFB3 at Ser466/Ser461 was increased in PE, being present in 77.4% (95% CI 59.9-88.9%) of PE and 8.3% (95% CI 1.2-27.0%) of NP samples (p < 0.001). PFKFB3 was more commonly expressed in PE, detected in 90.3% (95% CI 74.3-97.4%) of PE and 8.3% (95% CI 1.2-27.0%) of NP samples (p < 0.001). PFKFB4 had a 7.2-fold increase in expression in PE compared to NP (p < 0.001). No significant differences between NP and NC groups were observed. Regulatory proteins that increase glycolysis are increased in the urinary exosomes of subjects with pre-eclampsia, suggesting that renal glycolysis may be increased in this condition.en_US
dc.language.isoeng-
dc.subject6-Bisphosphataseen_US
dc.subject6-Phosphofructo-2-kinase/fructose-2en_US
dc.subjectGlycolysisen_US
dc.subjectPhosphorylationen_US
dc.subjectPre-eclampsiaen_US
dc.subjectUrinary exosomesen_US
dc.titleIncreased expression and phosphorylation of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase isoforms in urinary exosomes in pre-eclampsia.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Translational Medicineen_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.affiliationNephrologyen_US
dc.identifier.affiliationFaculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Australiaen_US
dc.identifier.affiliationMercy Hospital for Women, Heidelberg, Victoria, Australiaen_US
dc.identifier.doi10.1186/s12967-019-1806-6en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-7637-3661en_US
dc.identifier.orcid0000-0003-3983-0581en_US
dc.identifier.orcid0000-0001-5838-7779en_US
dc.identifier.pubmedid30819197-
dc.type.austinJournal Article-
local.name.researcherChoy, Suet-Wan
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptNephrology-
crisitem.author.deptNephrology-
crisitem.author.deptNephrology-
crisitem.author.deptNephrology-
crisitem.author.deptPharmacy-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptNephrology-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptMedicine (University of Melbourne)-
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