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细胞色素 b 还原酶 3 过表达和饮食烟酰胺核糖苷补充在衰老过程中促进小鼠肾脏远曲小管中独特的线粒体改变。

Cytochrome b reductase 3 overexpression and dietary nicotinamide riboside supplementation promote distinctive mitochondrial alterations in distal convoluted tubules of mouse kidneys during aging.

机构信息

Departamento de Biología Celular, Fisiología e Inmunología, Universidad de Córdoba, Campus de Excelencia Internacional Agroalimentario, Córdoba, Spain.

Experimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.

出版信息

Aging Cell. 2024 Nov;23(11):e14273. doi: 10.1111/acel.14273. Epub 2024 Jul 12.

DOI:10.1111/acel.14273
PMID:39001573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11561664/
Abstract

The kidney undergoes structural and physiological changes with age, predominantly studied in glomeruli and proximal tubules. However, limited knowledge is available about the impact of aging and anti-aging interventions on distal tubules. In this study, we investigated the effects of cytochrome b reductase 3 (CYB5R3) overexpression and/or dietary nicotinamide riboside (NR) supplementation on distal tubule mitochondria. Initially, transcriptomic data were analyzed to evaluate key genes related with distal tubules, CYB5R3, and NAD metabolism, showing significant differences between males and females in adult and old mice. Subsequently, our emphasis focused on assessing how these interventions, that have demonstrated the anti-aging potential, influenced structural parameters of distal tubule mitochondria, such as morphology and mass, as well as abundance, distance, and length of mitochondria-endoplasmic reticulum contact sites, employing an electron microscopy approach. Our findings indicate that both interventions have differential effects depending on the age and sex of the mice. Aging resulted in an increase in mitochondrial size and a decrease in mitochondrial abundance in males, while a reduction in abundance, size, and mitochondrial mass was observed in old females when compared with their adult counterparts. Combining both the interventions, CYB5R3 overexpression and dietary NR supplementation mitigated age-related changes; however, these effects were mainly accounted by NR in males and by transgenesis in females. In conclusion, the influence of CYB5R3 overexpression and dietary NR supplementation on distal tubule mitochondria depends on sex, genotype, and diet. This underscores the importance of incorporating these variables in subsequent studies to comprehensively address the multifaceted aspects of aging.

摘要

肾脏随着年龄的增长会发生结构和生理上的变化,这些变化主要在肾小球和近端小管中进行研究。然而,关于衰老和抗衰老干预对远端小管的影响,我们的了解还很有限。在这项研究中,我们调查了细胞色素 b 还原酶 3 (CYB5R3)过表达和/或饮食烟酰胺核糖 (NR)补充对远端小管线粒体的影响。首先,我们分析了转录组数据,以评估与远端小管、CYB5R3 和 NAD 代谢相关的关键基因,这些基因在成年和老年雄性和雌性小鼠之间存在显著差异。随后,我们的重点集中在评估这些干预措施如何影响远端小管线粒体的结构参数,如形态和质量,以及线粒体-内质网接触点的丰度、距离和长度,这些干预措施已经证明具有抗衰老的潜力。我们的研究结果表明,这两种干预措施都具有因年龄和性别而异的影响。衰老导致雄性小鼠的线粒体增大和线粒体丰度降低,而老年雌性小鼠的线粒体丰度、大小和线粒体质量减少,与成年雌性相比。与单独的干预措施相比,CYB5R3 过表达和饮食 NR 补充结合使用可以减轻与年龄相关的变化;然而,这些影响主要归因于雄性中的 NR 和雌性中的转基因。总之,CYB5R3 过表达和饮食 NR 补充对远端小管线粒体的影响取决于性别、基因型和饮食。这强调了在后续研究中纳入这些变量的重要性,以全面解决衰老的多方面问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11561664/ee03b1e3133d/ACEL-23-e14273-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11561664/eba2a10fdd2e/ACEL-23-e14273-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11561664/5d0f7c6c8505/ACEL-23-e14273-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11561664/8776d981f5cb/ACEL-23-e14273-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11561664/b172be344ec7/ACEL-23-e14273-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11561664/e4ea4800b4b4/ACEL-23-e14273-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11561664/ee03b1e3133d/ACEL-23-e14273-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11561664/eba2a10fdd2e/ACEL-23-e14273-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11561664/5d0f7c6c8505/ACEL-23-e14273-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11561664/8776d981f5cb/ACEL-23-e14273-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11561664/b172be344ec7/ACEL-23-e14273-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11561664/e4ea4800b4b4/ACEL-23-e14273-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11561664/ee03b1e3133d/ACEL-23-e14273-g006.jpg

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