Rapid isolation of urinary exosomal biomarkers using a nanomembrane ultrafiltration concentrator.

@article{citeulike:1414727, abstract = {Urinary exosomes are excreted from all nephron segments and may serve as biomarkers for classifying renal diseases. Isolation of urinary exosomes by the established ultracentrifugation method has some limitations for use in a clinical laboratory. We sought a rapid and simple way to obtain urinary exosomes. We used a commercially available nanomembrane concentrator to enrich exosomes from urine by centrifugation at 3,000 g for 10-30 min. Urinary exosomal markers tumor susceptibility gene 101, aquaporin-2, neuron-specific enolase, annexin V, angiotensin-converting enzyme, and podocalyxin (PODXL) were recovered from the nanomembrane concentrator and detected by Western blotting, and typical features of urinary vesicles were found by electron microscopy. Exosomal markers were detected in as little as 0.5 ml of urine. By the nanomembrane method, exosomal proteins could be recovered from urine samples frozen at -80 degrees C or refrigerated overnight at 4 degrees C then stored at -80 degrees C. By enriching exosomes we could detect PODXL, a podocyte marker, which decreased by 71\% in five male patients with focal segmental glomerulosclerosis and abundant proteinuria. We conclude that 1) use of a nanomembrane concentrator simplifies and accelerates the enrichment of urinary exosomes; and 2) the nanomembrane concentrator can concentrate exosomal proteins from clinical urine samples. This enhanced method may accelerate the translation of urinary exosomal biomarkers from bench to bedside for the diagnosis, classification, and prognostication of renal diseases.}, address = {Renal Diagnostics and Therapeutics Unit, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-1268, USA.}, author = {Cheruvanky, A. and Zhou, H. and Pisitkun, T. and Kopp, J. B. and Knepper, M. A. and Yuen, P. S. and Star, R. A. }, citeulike-article-id = {1414727}, doi = {10.1152/ajprenal.00434.2006}, issn = {0363-6127}, journal = {Am J Physiol Renal Physiol}, keywords = {proteomics, urine}, month = {May}, number = {5}, posted-at = {2007-06-27 03:41:21}, priority = {2}, title = {Rapid isolation of urinary exosomal biomarkers using a nanomembrane ultrafiltration concentrator.}, url = {http://dx.doi.org/10.1152/ajprenal.00434.2006}, volume = {292}, year = {2007} }

TY - JOUR ID - citeulike:1414727 L3 - citeulike-article-id:1414727 TI - Rapid isolation of urinary exosomal biomarkers using a nanomembrane ultrafiltration concentrator. JF - Am J Physiol Renal Physiol VL - 292 IS - 5 AD - Renal Diagnostics and Therapeutics Unit, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-1268, USA. SN - 0363-6127 N2 - Urinary exosomes are excreted from all nephron segments and may serve as biomarkers for classifying renal diseases. Isolation of urinary exosomes by the established ultracentrifugation method has some limitations for use in a clinical laboratory. We sought a rapid and simple way to obtain urinary exosomes. We used a commercially available nanomembrane concentrator to enrich exosomes from urine by centrifugation at 3,000 g for 10-30 min. Urinary exosomal markers tumor susceptibility gene 101, aquaporin-2, neuron-specific enolase, annexin V, angiotensin-converting enzyme, and podocalyxin (PODXL) were recovered from the nanomembrane concentrator and detected by Western blotting, and typical features of urinary vesicles were found by electron microscopy. Exosomal markers were detected in as little as 0.5 ml of urine. By the nanomembrane method, exosomal proteins could be recovered from urine samples frozen at -80 degrees C or refrigerated overnight at 4 degrees C then stored at -80 degrees C. By enriching exosomes we could detect PODXL, a podocyte marker, which decreased by 71% in five male patients with focal segmental glomerulosclerosis and abundant proteinuria. We conclude that 1) use of a nanomembrane concentrator simplifies and accelerates the enrichment of urinary exosomes; and 2) the nanomembrane concentrator can concentrate exosomal proteins from clinical urine samples. This enhanced method may accelerate the translation of urinary exosomal biomarkers from bench to bedside for the diagnosis, classification, and prognostication of renal diseases. KW - proteomics KW - urine AU - Cheruvanky, A AU - Zhou, H AU - Pisitkun, T AU - Kopp, JB AU - Knepper, MA AU - Yuen, PS AU - Star, RA PY - 2007/05// UR - http://dx.doi.org/10.1152/ajprenal.00434.2006 ER -