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Differential expression of aerobic oxidative metabolism-related proteins in diabetic urinary exosomes

BACKGROUND: As a metabolic disease, any abnormality in the aerobic oxidation pathway of glucose may lead to the occurrence of diabetes. This study aimed to investigate the changes in proteins related to aerobic oxidative metabolism in urinary exosomes of diabetic patients and normal controls of diff...

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Autores principales: Liu, Tianci, Wang, Yizhao, Zhao, Man, Jiang, Jun, Li, Tao, Zhang, Man
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515495/
https://www.ncbi.nlm.nih.gov/pubmed/36187097
http://dx.doi.org/10.3389/fendo.2022.992827
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author Liu, Tianci
Wang, Yizhao
Zhao, Man
Jiang, Jun
Li, Tao
Zhang, Man
author_facet Liu, Tianci
Wang, Yizhao
Zhao, Man
Jiang, Jun
Li, Tao
Zhang, Man
author_sort Liu, Tianci
collection PubMed
description BACKGROUND: As a metabolic disease, any abnormality in the aerobic oxidation pathway of glucose may lead to the occurrence of diabetes. This study aimed to investigate the changes in proteins related to aerobic oxidative metabolism in urinary exosomes of diabetic patients and normal controls of different ages, and to further verify their correlation with the pathogenesis of diabetes. METHODS: Samples were collected, and proteomic information of urinary exosomes was collected by LC-MS/MS. ELISA was used to further detect the expression of aerobic and oxidative metabolism-related proteins in urinary exosomes of diabetic patients and normal controls of different ages, and to draw receiver operating characteristic (ROC) curve to evaluate its value in diabetes monitoring. RESULTS: A total of 17 proteins involved in aerobic oxidative metabolism of glucose were identified in urinary exosome proteins. Compared with normal control, the expressions of PFKM, GAPDH, ACO2 and MDH2 in diabetic patients were decreased, and the expression of IDH3G was increased. The concentrations of PFKM, GAPDH and ACO2 in urinary exosomes were linearly correlated with the expression of MDH2 (P<0.05). These four proteins vary with age, with the maximum concentration in the 45-59 age group. PFKM, GAPDH, ACO2, and MDH2 in urinary exosomes have certain monitoring value. When used in combination, the AUC was 0.840 (95% CI 0.764-0.915). CONCLUSIONS: In diabetic patients, aerobic oxidative metabolism is reduced, and the expression of aerobic oxidative metabolism-related proteins PFKM, GAPDH, ACO2, and MDH2 in urinary exosomes is reduced, which may become potential biomarkers for monitoring changes in diabetes.
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spelling pubmed-95154952022-09-29 Differential expression of aerobic oxidative metabolism-related proteins in diabetic urinary exosomes Liu, Tianci Wang, Yizhao Zhao, Man Jiang, Jun Li, Tao Zhang, Man Front Endocrinol (Lausanne) Endocrinology BACKGROUND: As a metabolic disease, any abnormality in the aerobic oxidation pathway of glucose may lead to the occurrence of diabetes. This study aimed to investigate the changes in proteins related to aerobic oxidative metabolism in urinary exosomes of diabetic patients and normal controls of different ages, and to further verify their correlation with the pathogenesis of diabetes. METHODS: Samples were collected, and proteomic information of urinary exosomes was collected by LC-MS/MS. ELISA was used to further detect the expression of aerobic and oxidative metabolism-related proteins in urinary exosomes of diabetic patients and normal controls of different ages, and to draw receiver operating characteristic (ROC) curve to evaluate its value in diabetes monitoring. RESULTS: A total of 17 proteins involved in aerobic oxidative metabolism of glucose were identified in urinary exosome proteins. Compared with normal control, the expressions of PFKM, GAPDH, ACO2 and MDH2 in diabetic patients were decreased, and the expression of IDH3G was increased. The concentrations of PFKM, GAPDH and ACO2 in urinary exosomes were linearly correlated with the expression of MDH2 (P<0.05). These four proteins vary with age, with the maximum concentration in the 45-59 age group. PFKM, GAPDH, ACO2, and MDH2 in urinary exosomes have certain monitoring value. When used in combination, the AUC was 0.840 (95% CI 0.764-0.915). CONCLUSIONS: In diabetic patients, aerobic oxidative metabolism is reduced, and the expression of aerobic oxidative metabolism-related proteins PFKM, GAPDH, ACO2, and MDH2 in urinary exosomes is reduced, which may become potential biomarkers for monitoring changes in diabetes. Frontiers Media S.A. 2022-09-14 /pmc/articles/PMC9515495/ /pubmed/36187097 http://dx.doi.org/10.3389/fendo.2022.992827 Text en Copyright © 2022 Liu, Wang, Zhao, Jiang, Li and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Liu, Tianci
Wang, Yizhao
Zhao, Man
Jiang, Jun
Li, Tao
Zhang, Man
Differential expression of aerobic oxidative metabolism-related proteins in diabetic urinary exosomes
title Differential expression of aerobic oxidative metabolism-related proteins in diabetic urinary exosomes
title_full Differential expression of aerobic oxidative metabolism-related proteins in diabetic urinary exosomes
title_fullStr Differential expression of aerobic oxidative metabolism-related proteins in diabetic urinary exosomes
title_full_unstemmed Differential expression of aerobic oxidative metabolism-related proteins in diabetic urinary exosomes
title_short Differential expression of aerobic oxidative metabolism-related proteins in diabetic urinary exosomes
title_sort differential expression of aerobic oxidative metabolism-related proteins in diabetic urinary exosomes
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515495/
https://www.ncbi.nlm.nih.gov/pubmed/36187097
http://dx.doi.org/10.3389/fendo.2022.992827
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