不同国际肾脏病学会/肾脏病理学会分级狼疮性肾炎患者足细胞线粒体动力学。

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Qijiao Wei, Qing Yan, Shengli Zhang, Fei Gao, Zhihan Chen, He Lin, Li Sun
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引用次数: 0

摘要

线粒体细胞病和肾病综合征患者足细胞线粒体形态学改变。然而,狼疮性肾炎(LN)足细胞是否参与线粒体动力学尚不清楚。本研究旨在探讨线粒体形态与足细胞病变以及LN的实验室和病理特征之间的关系。电镜下观察足突宽度(FPW)和线粒体形态。然后在国际肾脏病学会/肾脏病理学会分级的LN患者中探讨线粒体形态与足细胞病变和实验室特征之间的关系。足突消失和足细胞线粒体过度分裂,蛋白尿与FPW呈正相关。线粒体面积、周长、纵横比与BUN呈负相关,24h-UTP与Alb呈正相关。同时,Alb与外形因子呈负相关。FPW、形状因子、表面密度和面积上数值密度与24h-UTP呈正相关。过度的线粒体分裂与足细胞损伤和蛋白尿有关,但其机制仍有待探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitochondrial Dynamics of Podocyte in Various International Society of Nephrology/Renal Pathology Society Class Lupus Nephritis Patients.

Morphological changes of podocyte mitochondria are observed in patients with mitochondrial cytopathy and nephrotic syndrome. However, whether mitochondrial dynamics involved in podocyte in lupus nephritis (LN) is still not clear. This study aims to investigate the associations between mitochondrial morphology and podocyte lesions and laboratory and pathological features in LN. The foot process width (FPW) and mitochondrial morphology were observed through electron microscope. Then the associations between mitochondrial morphology and podocyte lesions and laboratory features were explored in various International Society of Nephrology/Renal Pathology Society class LN patients. Foot process effacement and excessive mitochondria fission in podocyte were observed and proteinuria was positively correlated with FPW. Mitochondria area, circumference, and aspect ratio were negatively correlated with BUN, and 24h-UTP positively correlated with Alb. At the same time, Alb was negatively correlated with form factor. FPW, form factor, surface density, and numerical density on area were positively correlated with 24h-UTP. Excessive mitochondrial fission is associated with podocyte damage and proteinuria, whereas the mechanism still needs to be explored.

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来源期刊
DNA and cell biology
DNA and cell biology 生物-生化与分子生物学
CiteScore
6.60
自引率
0.00%
发文量
93
审稿时长
1.5 months
期刊介绍: DNA and Cell Biology delivers authoritative, peer-reviewed research on all aspects of molecular and cellular biology, with a unique focus on combining mechanistic and clinical studies to drive the field forward. DNA and Cell Biology coverage includes: Gene Structure, Function, and Regulation Gene regulation Molecular mechanisms of cell activation Mechanisms of transcriptional, translational, or epigenetic control of gene expression Molecular Medicine Molecular pathogenesis Genetic approaches to cancer and autoimmune diseases Translational studies in cell and molecular biology Cellular Organelles Autophagy Apoptosis P bodies Peroxisosomes Protein Biosynthesis and Degradation Regulation of protein synthesis Post-translational modifications Control of degradation Cell-Autonomous Inflammation and Host Cell Response to Infection Responses to cytokines and other physiological mediators Evasive pathways of pathogens.
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