MicroRNA-29c in urinary exosome/microvesicle as a biomarker of renal fibrosis

被引:236
作者
Lv, Lin-Li [1 ]
Cao, Yu-Han [1 ]
Ni, Hai-Feng [1 ]
Xu, Min [1 ]
Liu, Dan [1 ]
Liu, Hong [1 ]
Chen, Ping-Sheng [1 ]
Liu, Bi-Cheng [1 ]
机构
[1] Southeast Univ, Inst Nephrol, Zhongda Hosp, Sch Med, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
biomarker; exosome; microrna; tubulointerstitial fibrosis; urine; INTERSTITIAL FIBROSIS; CIRCULATING MICRORNAS; FUNCTIONAL MICRORNAS; EXOSOMES; EXPRESSION; MECHANISM; RNA; EXOSOMES/MICROVESICLES; CELLS;
D O I
10.1152/ajprenal.00148.2013
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Lv LL, Cao YH, Ni HF, Xu M, Liu D, Liu H, Chen PS, Liu BC. MicroRNA-29c in urinary exosome/microvesicle as a biomarker of renal fibrosis. Am J Physiol Renal Physiol 305: F1220-F1227, 2013. First published August 14, 2013; doi:10.1152/ajprenal.00148.2013.-Micro (mi)RNAs are frequently dysregulated in the development of renal fibrosis. Exosomes are small membrane vesicles that could be isolated from urine secreted from all nephron segments. Here we sought to observe for the first time whether miRNA in urine exosome could serve as a potential biomarker of renal fibrosis. Urine samples were collected from 32 chronic kidney disease (CKD) patients who underwent kidney biopsy and 7 controls. Exosome was isolated and confirmed by immunogold staining of exosome marker. Members of miR-29, miR-200, and RNU6B as endogenous control were detected by RT quantitative PCR. Electronic microscopy verified a typical shape of exosome with average size of 65.1 nm and labeled it with anti-CD9 and anti-aquaporin 2 antibody. Members of miR-29 and miR-200 are readily measured with reduced levels compared with controls (P < 0.05) and can robustly distinguish CKD from controls [area under the curve (AUC) varied from 0.902 to 1 by receiver operating characteristics analysis]. miR-29c correlated with both estimated glomerular filtration rate (r = 0.362; P < 0.05) and degree of tubulointerstitial fibrosis (r = -0.359; P < 0.05) for CKD patients. Moreover, miRNA in exosome was decreased in mild fibrosis group compared with moderated to severe group. miR-29a and miR-29c could predict degree of tubulointerstitial fibrosis with AUC of 0.883 and 0.738 (P < 0.05). The sensitivity and specificity for distinguishing mild from moderate to severe fibrosis were 93.8 and 81.3% with the use of miR-29a and 68.8 and 81.3% for miR-29c. Overall, miR-29c in urinary exosome correlates with both renal function and degree of histological fibrosis, suggesting it as a novel, noninvasive marker for renal fibrosis.
引用
收藏
页码:F1220 / F1227
页数:8
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