Nucleic acids within urinary exosomes/microvesicles are potential biomarkers for renal disease

被引:345
作者
Miranda, Kevin C. [1 ]
Bond, Daniel T. [1 ]
McKee, Mary [1 ]
Skog, Johan [2 ,3 ,4 ,5 ,6 ]
Paunescu, Teodor G. [1 ]
Da Silva, Nicolas [1 ]
Brown, Dennis [1 ]
Russo, Leileata M. [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Program Membrane Biol, Boston, MA 02114 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Nephrol,Ctr Syst Biol, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Charlestown, MA USA
[4] Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA USA
[5] Massachusetts Gen Hosp, Dept Radiol, Charlestown, MA USA
[6] Massachusetts Gen Hosp, Neurosci Program, Charlestown, MA USA
关键词
acute kidney injury; chronic kidney disease; exosome; transcriptional profiling; EXOSOMES; MARKER; ATPASE; CELLS; RNAS;
D O I
10.1038/ki.2010.106
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Urinary exosomes or microvesicles are being studied intensively to identify potential new biomarkers for renal disease. We sought to identify whether these microvesicles contain nucleic acids. We isolated microvesicles from human urine in the same density range as that previously described for urinary exosomes and found them to have an RNA integrity profile similar to that of kidney tissue, including 18S and 28S rRNA. This profile was better preserved in urinary microvesicles compared with whole cells isolated from urine, suggesting that microvesicles may protect RNA during urine passage. We were able to detect mRNA in the human urinary microvesicles encoding proteins from all regions of the nephron and the collecting duct. Further, to provide a proof of principle, we found that microvesicles isolated from the urine of the V-ATPase B1 subunit knockout mice lacked mRNA of this subunit while containing a normal amount of the B2 subunit and aquaporin 2. The microvesicles were found to be contaminated with extraneous DNA potentially on their surface; therefore, we developed a rapid and reliable means to isolate nucleic acids from within urine microvesicles devoid of this extraneous contamination. Our study provides an experimental strategy for the routine isolation and use of urinary microvesicles as a novel and non-invasive source of nucleic acids to further renal disease biomarker discovery. Kidney International (2010) 78, 191-199; doi:10.1038/ki.2010.106; published online 28 April 2010
引用
收藏
页码:191 / 199
页数:9
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