de Rijk Mathijs M, Wolf-Johnston Amanda, Kullmann Aura F, Taiclet Stephanie, Kanai Anthony J, Shiva Sruti, Birder Lori A
Department of Urology, School for Mental Health and Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands.
Department of Urology, Maastricht University Medical Center+ (MUMC+), Maastricht, The Netherlands.
Int Neurourol J. 2022 Jun;26(2):111-118. doi: 10.5213/inj.2142224.112. Epub 2022 Jun 30.
Lower urinary tract symptoms are known to significantly increase with age, negatively impacting quality of life and self-reliance. The urothelium fulfills crucial tasks, serving as a barrier protecting the underlying bladder tissue from the harsh chemical composition of urine, and exhibits signaling properties via the release of mediators within the bladder wall that affect bladder functioning. Aging is associated with detrimental changes in cellular health, in part by increasing oxidative stress in the bladder mucosa, and more specifically the urothelium. This, in turn, may impact urothelial mitochondrial health and bioenergetics.
We collected mucosal tissue samples from both young (3-4 months old) and aged (25-30 months old) rats. Tissue was evaluated for p21-Arc, nitrotyrosine, and cytochrome C expression by western immunoblotting. Urothelial cells were cultured for single-cell imaging to analyze basal levels of reactive oxygen species and the mitochondrial membrane potential. Mitochondrial bioenergetics and cellular respiration were investigated by the Seahorse assay, and measurements of adenosine triphosphate release were made using the luciferin-luciferase assay.
Aging was associated with a significant increase in biomarkers of cellular senescence, oxidative stress, and basal levels of reactive oxygen species. The mitochondrial membrane potential was significantly lower in urothelial cell cultures from aged animals, and cultures from aged animals showed a significant decrease in mitochondrial bioenergetics.
Aging-related increases in oxidative stress and excessive reactive oxygen species may be contributing factors underlying lower urinary tract symptoms in older adults. The mechanisms outlined in this study could be utilized to identify novel pharmaceutical targets to improve aging-associated bladder dysfunction.
已知下尿路症状会随着年龄的增长而显著增加,对生活质量和自理能力产生负面影响。尿路上皮执行着关键任务,作为一种屏障保护膀胱下方组织免受尿液恶劣化学成分的侵害,并通过在膀胱壁内释放影响膀胱功能的介质来展现信号传导特性。衰老与细胞健康的有害变化相关,部分原因是膀胱黏膜,尤其是尿路上皮中的氧化应激增加。这进而可能影响尿路上皮线粒体的健康和生物能量学。
我们从年轻(3 - 4个月大)和年老(25 - 30个月大)的大鼠身上收集了黏膜组织样本。通过蛋白质免疫印迹法评估组织中p21 - Arc、硝基酪氨酸和细胞色素C的表达。培养尿路上皮细胞用于单细胞成像,以分析活性氧的基础水平和线粒体膜电位。通过海马实验研究线粒体生物能量学和细胞呼吸,并使用荧光素 - 荧光素酶测定法测量三磷酸腺苷的释放。
衰老与细胞衰老、氧化应激的生物标志物以及活性氧基础水平的显著增加相关。来自老年动物的尿路上皮细胞培养物中的线粒体膜电位显著更低,并且来自老年动物的培养物显示线粒体生物能量学显著下降。
与衰老相关的氧化应激增加和过量的活性氧可能是老年人下尿路症状的潜在促成因素。本研究中概述的机制可用于识别新的药物靶点,以改善与衰老相关的膀胱功能障碍。