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足细胞中精氨酸酶-II 的升高导致雄性小鼠与年龄相关的白蛋白尿。

Elevation of Arginase-II in Podocytes Contributes to Age-Associated Albuminuria in Male Mice.

机构信息

Laboratory of Cardiovascular and Aging Research, Department of Endocrinology, Metabolism and Cardiovascular System, Faculty of Science and Medicine, University of Fribourg, Chemin du Musée 5, CH-1700 Fribourg, Switzerland.

出版信息

Int J Mol Sci. 2023 Jul 7;24(13):11228. doi: 10.3390/ijms241311228.

Abstract

One of the manifestations of renal aging is podocyte dysfunction and loss, which are associated with proteinuria and glomerulosclerosis. Studies show a male bias in glomerular dysfunction and chronic kidney diseases, and the underlying mechanisms remain obscure. Recent studies demonstrate the role of an age-associated increase in arginase-II (Arg-II) in proximal tubules of both male and female mice. However, it is unclear whether Arg-II is also involved in aging glomeruli. The current study investigates the role of the sex-specific elevation of Arg-II in podocytes in age-associated increased albuminuria. Young (3-4 months) and old (20-22 months) male and female mice of and arginase-II knockout () were used. Albuminuria was employed as a readout of glomerular function. Cellular localization and expression of Arg-II in glomeruli were analyzed using an immunofluorescence confocal microscope. A more pronounced age-associated increase in albuminuria was found in male than in female mice. An age-associated induction of Arg-II in glomeruli and podocytes (as demonstrated by co-localization of Arg-II with the podocyte marker synaptopodin) was also observed in males but not in females. Ablation of the gene in mice significantly reduces age-associated albuminuria in males. Also, age-associated decreases in podocyte density and glomerulus hypertrophy are significantly prevented in male but not in female mice. However, age-associated glomerulosclerosis is not affected by ablation in both sexes. These results demonstrate a role of Arg-II in sex-specific podocyte injury in aging. They may explain the sex-specific differences in the development of renal disease in humans during aging.

摘要

肾脏老化的表现之一是足细胞功能障碍和丧失,这与蛋白尿和肾小球硬化有关。研究表明,肾小球功能障碍和慢性肾脏病存在男性偏向,但其潜在机制尚不清楚。最近的研究表明,在雄性和雌性小鼠的近端肾小管中,一种与年龄相关的精氨酸酶-II(Arg-II)增加与这种情况有关。然而,Arg-II 是否也参与了老化的肾小球,目前尚不清楚。本研究探讨了在与年龄相关的白蛋白尿增加中,足细胞中 Arg-II 的性别特异性升高所起的作用。使用年轻(3-4 个月)和年老(20-22 个月)雄性和雌性 小鼠和 Arg-II 基因敲除()小鼠。白蛋白尿被用作肾小球功能的读数。使用免疫荧光共聚焦显微镜分析肾小球中 Arg-II 的细胞定位和表达。与雌性小鼠相比,雄性小鼠的白蛋白尿与年龄相关的增加更为明显。在雄性小鼠中观察到与年龄相关的肾小球和足细胞中 Arg-II 的诱导(如 Arg-II 与足细胞标记物 synaptopodin 的共定位所证明),但在雌性小鼠中没有观察到。在雄性小鼠中,基因敲除可显著降低与年龄相关的白蛋白尿。此外,在雄性 小鼠中,与年龄相关的足细胞密度降低和肾小球肥大显著得到预防,但在雌性小鼠中则不然。然而,在两性中,与年龄相关的肾小球硬化均不受 基因敲除的影响。这些结果表明 Arg-II 在与年龄相关的足细胞损伤中具有性别特异性作用。它们可能解释了在人类衰老过程中,肾脏疾病在两性中发展的性别特异性差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c986/10342439/05c9a38b68cb/ijms-24-11228-g001.jpg

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