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Comparison of Human Urinary Exosomes Isolated via Ultracentrifugation Alone versus Ultracentrifugation Followed by SEC Column-Purification.
Huang, Kun; Garimella, Sudha; Clay-Gilmour, Alyssa; Vojtech, Lucia; Armstrong, Bridget; Bessonny, Madison; Stamatikos, Alexis.
Affiliation
  • Huang K; Department of Food, Nutrition, and Packaging Sciences, Clemson University, Clemson, SC 29634, USA.
  • Garimella S; Prisma Health, Pediatric Nephrology, Greenville, SC 29615, USA.
  • Clay-Gilmour A; Department of Epidemiology & Biostatistics, Arnold School of Public Health, University of South Carolina, Columbia, SC 29208, USA.
  • Vojtech L; Department of Obstetrics & Gynecology, University of Washington, Seattle, WA 98109, USA.
  • Armstrong B; Department of Exercise Science, Arnold School of Public Health, University of South Carolina, Columbia, SC 29208, USA.
  • Bessonny M; Department of Epidemiology & Biostatistics, Arnold School of Public Health, University of South Carolina, Columbia, SC 29208, USA.
  • Stamatikos A; Department of Food, Nutrition, and Packaging Sciences, Clemson University, Clemson, SC 29634, USA.
J Pers Med ; 12(3)2022 Feb 24.
Article in En | MEDLINE | ID: mdl-35330340
ABSTRACT
Chronic kidney disease is a progressive, incurable condition that involves a gradual loss of kidney function. While there are no non-invasive biomarkers available to determine whether individuals are susceptible to developing chronic kidney disease, small RNAs within urinary exosomes have recently emerged as a potential candidate to use for assessing renal function. Ultracentrifugation is the gold standard for urinary exosome isolation. However, extravesicular small RNA contamination can occur when isolating exosomes from biological fluids using ultracentrifugation, which may lead to misidentifying the presence of certain small RNA species in human urinary exosomes. Therefore, we characterized human urinary exosomal preparations isolated by ultracentrifugation alone, or via ultracentrifugation followed by size exclusion chromatography (SEC) column-purification. Using nanoparticle tracking analysis, we identified SEC fractions containing robust amounts of exosome-sized particles, that we further characterized using immunoblotting. When compared to exosomal preparations isolated by ultracentrifugation only, SEC fractionated exosomal preparations showed higher levels of the exosome-positive marker CD81. Moreover, while the exosome-negative marker calnexin was undetectable in SEC fractionated exosomal preparations, we did observe calnexin detection in the exosomal preparations isolated by ultracentrifugation alone, which implies contamination in these preparations. Lastly, we imaged SEC fractionated exosomal preparations using transmission electron microscopy to confirm these preparations contained human urinary exosomes. Our results indicate that combining ultracentrifugation and SEC column-purification exosome isolation strategies is a powerful approach for collecting contaminant-free human urinary exosomes and should be considered when exosomes devoid of contamination are needed for downstream applications.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Pers Med Year: 2022 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Pers Med Year: 2022 Document type: Article Affiliation country: Estados Unidos