Differential synchrotron X-ray imaging markers based on the renal microvasculature for tubulointerstitial lesions and glomerulopathy

Abstract High resolution synchrotron microtomography capable of revealing microvessels in three dimensional (3D) establishes distinct imaging markers of mouse kidney disease strongly associated to renal tubulointerstitial (TI) lesions and glomerulopathy. Two complementary mouse models of chronic kid...

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Autores principales: Yu-Chuan Lin, Yeukuang Hwu, Guo-Shu Huang, Michael Hsiao, Tsung-Tse Lee, Shun-Min Yang, Ting-Kuo Lee, Nan-Yow Chen, Sung-Sen Yang, Ann Chen, Shuk-Man Ka
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/b46495e4cc53411eb6c3b74623caa271
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spelling oai:doaj.org-article:b46495e4cc53411eb6c3b74623caa2712021-12-02T11:52:41ZDifferential synchrotron X-ray imaging markers based on the renal microvasculature for tubulointerstitial lesions and glomerulopathy10.1038/s41598-017-03677-x2045-2322https://doaj.org/article/b46495e4cc53411eb6c3b74623caa2712017-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-03677-xhttps://doaj.org/toc/2045-2322Abstract High resolution synchrotron microtomography capable of revealing microvessels in three dimensional (3D) establishes distinct imaging markers of mouse kidney disease strongly associated to renal tubulointerstitial (TI) lesions and glomerulopathy. Two complementary mouse models of chronic kidney disease (CKD), unilateral ureteral obstruction (UUO) and focal segmental glomerulosclerosis (FSGS), were used and five candidates of unique 3D imaging markers were identified. Our characterization to differentially reflect the altered microvasculature of renal TI lesions and/or glomerulopathy demonstrated these image features can be used to differentiate the disease status and the possible cause therefore qualified as image markers. These 3D imaging markers were further correlated with the histopathology and renal microvessel-based molecular study using antibodies against vascular endothelial cells (CD31), the connective tissue growth factor or the vascular endothelial growth factor. We also found that these 3D imaging markers individually characterize the development of renal TI lesions or glomerulopathy, quantitative and integrated use of all of them provide more information for differentiating the two renal conditions. Our findings thus establish a practical strategy to characterize the CKD-associated renal injuries by the microangiography-based 3D imaging and highlight the impact of dysfunctional microvasculature as a whole on the pathogenesis of the renal lesions.Yu-Chuan LinYeukuang HwuGuo-Shu HuangMichael HsiaoTsung-Tse LeeShun-Min YangTing-Kuo LeeNan-Yow ChenSung-Sen YangAnn ChenShuk-Man KaNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yu-Chuan Lin
Yeukuang Hwu
Guo-Shu Huang
Michael Hsiao
Tsung-Tse Lee
Shun-Min Yang
Ting-Kuo Lee
Nan-Yow Chen
Sung-Sen Yang
Ann Chen
Shuk-Man Ka
Differential synchrotron X-ray imaging markers based on the renal microvasculature for tubulointerstitial lesions and glomerulopathy
description Abstract High resolution synchrotron microtomography capable of revealing microvessels in three dimensional (3D) establishes distinct imaging markers of mouse kidney disease strongly associated to renal tubulointerstitial (TI) lesions and glomerulopathy. Two complementary mouse models of chronic kidney disease (CKD), unilateral ureteral obstruction (UUO) and focal segmental glomerulosclerosis (FSGS), were used and five candidates of unique 3D imaging markers were identified. Our characterization to differentially reflect the altered microvasculature of renal TI lesions and/or glomerulopathy demonstrated these image features can be used to differentiate the disease status and the possible cause therefore qualified as image markers. These 3D imaging markers were further correlated with the histopathology and renal microvessel-based molecular study using antibodies against vascular endothelial cells (CD31), the connective tissue growth factor or the vascular endothelial growth factor. We also found that these 3D imaging markers individually characterize the development of renal TI lesions or glomerulopathy, quantitative and integrated use of all of them provide more information for differentiating the two renal conditions. Our findings thus establish a practical strategy to characterize the CKD-associated renal injuries by the microangiography-based 3D imaging and highlight the impact of dysfunctional microvasculature as a whole on the pathogenesis of the renal lesions.
format article
author Yu-Chuan Lin
Yeukuang Hwu
Guo-Shu Huang
Michael Hsiao
Tsung-Tse Lee
Shun-Min Yang
Ting-Kuo Lee
Nan-Yow Chen
Sung-Sen Yang
Ann Chen
Shuk-Man Ka
author_facet Yu-Chuan Lin
Yeukuang Hwu
Guo-Shu Huang
Michael Hsiao
Tsung-Tse Lee
Shun-Min Yang
Ting-Kuo Lee
Nan-Yow Chen
Sung-Sen Yang
Ann Chen
Shuk-Man Ka
author_sort Yu-Chuan Lin
title Differential synchrotron X-ray imaging markers based on the renal microvasculature for tubulointerstitial lesions and glomerulopathy
title_short Differential synchrotron X-ray imaging markers based on the renal microvasculature for tubulointerstitial lesions and glomerulopathy
title_full Differential synchrotron X-ray imaging markers based on the renal microvasculature for tubulointerstitial lesions and glomerulopathy
title_fullStr Differential synchrotron X-ray imaging markers based on the renal microvasculature for tubulointerstitial lesions and glomerulopathy
title_full_unstemmed Differential synchrotron X-ray imaging markers based on the renal microvasculature for tubulointerstitial lesions and glomerulopathy
title_sort differential synchrotron x-ray imaging markers based on the renal microvasculature for tubulointerstitial lesions and glomerulopathy
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/b46495e4cc53411eb6c3b74623caa271
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