蛋白尿
微泡
纳米粒子跟踪分析
外体
尿
蛋白尿
白蛋白
肾病
肾病科
细胞外小泡
泌尿科
医学
内科学
内分泌学
肾功能
化学
肾
生物
小RNA
糖尿病
细胞生物学
基因
生物化学
作者
Jonathan Gleadle,Kym McNicholas,Jordan Li,Michael Michael,Darling Rojas-Canales
标识
DOI:10.1681/asn.2018020115
摘要
In the article by Lv et al.1 published in the Journal of the American Society of Nephrology, the authors describe enhanced urinary exosomal release in experimental models of acute and chronic renal injury. They also describe increased exosomal release in patients with IgA nephropathy and a correlation between exosomal concentration and proteinuria. These findings are of clear interest, but we have reservations about some of the methodology used to ascertain this observation. They use nanoparticle tracking analysis (NTA) of urine and describe enhanced particle concentration in patients who are proteinuric. We have recently reported similar observations using NTA in 32 patients with varying levels of albuminuria.2 We found that albuminuria confounded particle analysis by NTA, because albumin-containing solutions contain particles of exosome-like size, and such particles can mimic exosomes in standard NTA. Immunodepletion of albumin from proteinuric urine resulted in a substantial reduction in the concentration of particles detected by NTA as did urine purification using iodixanol density gradients. More importantly, NTA measurements of pure albumin solutions yielded a substantial number of particles with a diameter of 105 nm. This reinforces the need for great caution in the interpretation of NTA results in fluids that have significant levels of protein. It also emphasizes the importance of stringent methods of purification, such as density gradients, in exosome analysis as recommended by the International Society for Extracellular Vesicles.3 Disclosures None.
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