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