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基于肾微血管的差示同步辐射 X 射线成像标志物用于肾小管间质性病变和肾小球病。

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

机构信息

Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan.

Institute of Physics, Academia Sinica, Taipei, Taiwan.

出版信息

Sci Rep. 2017 Jun 14;7(1):3488. doi: 10.1038/s41598-017-03677-x.

DOI:10.1038/s41598-017-03677-x
PMID:28615647
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5471266/
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.

摘要

高分辨率同步加速器微断层成像技术能够在三维(3D)中显示微血管,为小鼠肾脏疾病建立了独特的成像标志物,这些标志物与肾小管间质(TI)病变和肾小球病变密切相关。我们使用了两种慢性肾脏病(CKD)的互补小鼠模型,单侧输尿管梗阻(UUO)和局灶节段性肾小球硬化(FSGS),并确定了五个独特的 3D 成像标志物候选物。我们的特征分析表明,这些改变的微血管成像标志物可以区分肾脏 TI 病变和/或肾小球病变的不同状态,因此可以作为成像标志物。这些 3D 成像标志物还与使用抗血管内皮细胞(CD31)、结缔组织生长因子或血管内皮生长因子的抗体进行的组织病理学和肾脏基于微血管的分子研究相关联。我们还发现,这些 3D 成像标志物可以单独描述肾脏 TI 病变或肾小球病变的发展,对所有标志物进行定量和综合使用可以提供更多信息,以区分两种肾脏情况。我们的研究结果因此建立了一种通过基于微血管成像的 3D 成像来描述 CKD 相关肾脏损伤的实用策略,并强调了功能失调的微血管作为一个整体对肾脏病变发病机制的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e00a/5471266/63eef2b3ed2d/41598_2017_3677_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e00a/5471266/8f410881e05e/41598_2017_3677_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e00a/5471266/bd72829fd30b/41598_2017_3677_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e00a/5471266/f6e303eae7c3/41598_2017_3677_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e00a/5471266/a6388eb8a5db/41598_2017_3677_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e00a/5471266/63eef2b3ed2d/41598_2017_3677_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e00a/5471266/8f410881e05e/41598_2017_3677_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e00a/5471266/24e9ef560e12/41598_2017_3677_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e00a/5471266/488d14957eb8/41598_2017_3677_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e00a/5471266/bd72829fd30b/41598_2017_3677_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e00a/5471266/f6e303eae7c3/41598_2017_3677_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e00a/5471266/a6388eb8a5db/41598_2017_3677_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e00a/5471266/63eef2b3ed2d/41598_2017_3677_Fig7_HTML.jpg

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