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尿酸和钙结石形成者与非结石形成者尿液中外泌体尿酸转运体的差异。

Differences of Uric Acid Transporters Carrying Extracellular Vesicles in the Urine from Uric Acid and Calcium Stone Formers and Non-Stone Formers.

机构信息

School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 100029, China.

Division of Nephrology and Hypertension, Mayo Clinic College of Medicine, 200 1st Street SW, Rochester, MN 55905, USA.

出版信息

Int J Mol Sci. 2022 Sep 2;23(17):10010. doi: 10.3390/ijms231710010.

Abstract

Background: Low urine pH and volume are established risk factors for uric acid (UA) stone disease (UASD). Renal tubular epithelial cells exposed to an acidic pH and/or UA crystals can shed extracellular vesicles (EVs) into the tubular fluid, and these EVs may be a pathogenic biomarker of UASD. Methods: Urinary EVs bearing UA transporters (SLC2A9, SLC17A3, SLC22A12, SLC5A8, ABCG2, and ZNF365) were quantified in urine from UA stone formers (UASFs), calcium stone formers (CSFs), and age-/sex-matched non-stone formers (NSFs) using a standardized and published method of digital flow cytometry. Results: Urinary pH was lower (p < 0.05) and serum and urinary UA were greater (p < 0.05) in UASFs compared with NSFs. Urinary EVs carrying SLC17A3 and SLC5A8 were lower (p < 0.05) in UASFs compared with NSFs. Urinary EVs bearing SLC2A9, SLC22A12, SLC5A8, ABCG2, and ZNF365 were lower (p < 0.05) in CSFs than UASFs, while excretion of SLC17A3-bearing EVs did not differ between groups. Conclusion: EVs bearing specific UA transporters might contribute to the pathogenesis of UASD and represent non-invasive pathogenic biomarkers for calcium and UA stone risk.

摘要

背景

低尿 pH 值和低尿量是尿酸(UA)结石病(UASD)的既定危险因素。暴露于酸性 pH 值和/或 UA 晶体的肾小管上皮细胞会将细胞外囊泡(EVs)排入管状液中,这些 EVs 可能是 UASD 的致病生物标志物。方法:使用数字流式细胞术的标准化和已发表方法,定量测定 UA 结石形成者(UASFs)、钙结石形成者(CSFs)和年龄/性别匹配的非结石形成者(NSFs)尿液中携带 UA 转运体(SLC2A9、SLC17A3、SLC22A12、SLC5A8、ABCG2 和 ZNF365)的尿 EVs。结果:与 NSFs 相比,UASFs 的尿 pH 值更低(p<0.05),血清和尿 UA 更高(p<0.05)。与 NSFs 相比,UASFs 的尿液 EVs 携带 SLC17A3 和 SLC5A8 更少(p<0.05)。与 UASFs 相比,CSFs 的尿液 EVs 携带 SLC2A9、SLC22A12、SLC5A8、ABCG2 和 ZNF365 更少(p<0.05),而携带 SLC17A3 的 EVs 的排泄量在两组之间没有差异。结论:携带特定 UA 转运体的 EVs 可能有助于 UASD 的发病机制,并代表钙和 UA 结石风险的非侵入性致病生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ce7/9456222/5b251108ddb3/ijms-23-10010-g001.jpg

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