Cargando…

Advanced glycation end product (AGE) modified proteins in tears of diabetic patients

PURPOSE: High glucose level in diabetic patients may lead to advanced glycation end product (AGE) modified proteins. This study investigated AGE modified proteins in tears and compared their levels in diabetic patients (DM) with non-diabetic controls (CTL). METHODS: Basal tears were collected from D...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Zhenjun, Liu, Jingfang, Shi, Bingyin, He, Shuixiang, Yao, Xiaoli, Willcox, Mark D.P.
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2927418/
https://www.ncbi.nlm.nih.gov/pubmed/20806041
_version_ 1782185747961348096
author Zhao, Zhenjun
Liu, Jingfang
Shi, Bingyin
He, Shuixiang
Yao, Xiaoli
Willcox, Mark D.P.
author_facet Zhao, Zhenjun
Liu, Jingfang
Shi, Bingyin
He, Shuixiang
Yao, Xiaoli
Willcox, Mark D.P.
author_sort Zhao, Zhenjun
collection PubMed
description PURPOSE: High glucose level in diabetic patients may lead to advanced glycation end product (AGE) modified proteins. This study investigated AGE modified proteins in tears and compared their levels in diabetic patients (DM) with non-diabetic controls (CTL). METHODS: Basal tears were collected from DM with (DR) or without (DNR) retinopathy and CTL. Total AGE modified proteins were detected quantitatively by a dot immunobinding assay. The AGE modified proteins were separated in 1D- and 2D-SDS gels and detected by western-blotting. The individual AGE modified proteins were also compared between groups using densitometry. RESULTS: Compared with the CTL group, tear concentrations of AGE modified proteins were significantly elevated in DR and DNR groups. The concentration of AGE modified proteins in diabetic tears were positively correlated with AGE modified hemoglobin (HbA1c) and postprandial blood glucose level (PBG). Western blotting of AGE modified proteins from 1D-SDS gels showed several bands, the major one at around 60 kDa. The intensities of AGE modified protein bands were higher in DM tears than in CTL tears. Western blotting from 2D-SDS gels showed a strongly stained horizontal strip, which corresponded to the major band in 1D-SDS gels. Most of the other AGE modified protein species were within molecular weight of 30–60 kDa, PI 5.2–7.0. Densitometry analysis demonstrated several AGE modified proteins were elevated in DR or DNR tears. CONCLUSIONS: Total and some individual AGE modified proteins were elevated in DM tears. AGE modified proteins in tears may be used as biomarkers to diagnose diabetes and/or diabetic retinopathy.
format Text
id pubmed-2927418
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Molecular Vision
record_format MEDLINE/PubMed
spelling pubmed-29274182010-08-30 Advanced glycation end product (AGE) modified proteins in tears of diabetic patients Zhao, Zhenjun Liu, Jingfang Shi, Bingyin He, Shuixiang Yao, Xiaoli Willcox, Mark D.P. Mol Vis Research Article PURPOSE: High glucose level in diabetic patients may lead to advanced glycation end product (AGE) modified proteins. This study investigated AGE modified proteins in tears and compared their levels in diabetic patients (DM) with non-diabetic controls (CTL). METHODS: Basal tears were collected from DM with (DR) or without (DNR) retinopathy and CTL. Total AGE modified proteins were detected quantitatively by a dot immunobinding assay. The AGE modified proteins were separated in 1D- and 2D-SDS gels and detected by western-blotting. The individual AGE modified proteins were also compared between groups using densitometry. RESULTS: Compared with the CTL group, tear concentrations of AGE modified proteins were significantly elevated in DR and DNR groups. The concentration of AGE modified proteins in diabetic tears were positively correlated with AGE modified hemoglobin (HbA1c) and postprandial blood glucose level (PBG). Western blotting of AGE modified proteins from 1D-SDS gels showed several bands, the major one at around 60 kDa. The intensities of AGE modified protein bands were higher in DM tears than in CTL tears. Western blotting from 2D-SDS gels showed a strongly stained horizontal strip, which corresponded to the major band in 1D-SDS gels. Most of the other AGE modified protein species were within molecular weight of 30–60 kDa, PI 5.2–7.0. Densitometry analysis demonstrated several AGE modified proteins were elevated in DR or DNR tears. CONCLUSIONS: Total and some individual AGE modified proteins were elevated in DM tears. AGE modified proteins in tears may be used as biomarkers to diagnose diabetes and/or diabetic retinopathy. Molecular Vision 2010-08-11 /pmc/articles/PMC2927418/ /pubmed/20806041 Text en Copyright © 2010 Molecular Vision. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhao, Zhenjun
Liu, Jingfang
Shi, Bingyin
He, Shuixiang
Yao, Xiaoli
Willcox, Mark D.P.
Advanced glycation end product (AGE) modified proteins in tears of diabetic patients
title Advanced glycation end product (AGE) modified proteins in tears of diabetic patients
title_full Advanced glycation end product (AGE) modified proteins in tears of diabetic patients
title_fullStr Advanced glycation end product (AGE) modified proteins in tears of diabetic patients
title_full_unstemmed Advanced glycation end product (AGE) modified proteins in tears of diabetic patients
title_short Advanced glycation end product (AGE) modified proteins in tears of diabetic patients
title_sort advanced glycation end product (age) modified proteins in tears of diabetic patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2927418/
https://www.ncbi.nlm.nih.gov/pubmed/20806041
work_keys_str_mv AT zhaozhenjun advancedglycationendproductagemodifiedproteinsintearsofdiabeticpatients
AT liujingfang advancedglycationendproductagemodifiedproteinsintearsofdiabeticpatients
AT shibingyin advancedglycationendproductagemodifiedproteinsintearsofdiabeticpatients
AT heshuixiang advancedglycationendproductagemodifiedproteinsintearsofdiabeticpatients
AT yaoxiaoli advancedglycationendproductagemodifiedproteinsintearsofdiabeticpatients
AT willcoxmarkdp advancedglycationendproductagemodifiedproteinsintearsofdiabeticpatients