MicroRNA expression profiling in peritoneal fibrosis

被引:26
作者
Morishita, Yoshiyuki [1 ]
Yoshizawa, Hiromichi
Watanabe, Minami
Imai, Reika
Imai, Toshimi
Hirahara, Ichiro
Akimoto, Tetsu
Ookawara, Susumu
Muto, Shigeaki
Nagata, Daisuke
机构
[1] Jichi Med Univ, Saitama Med Ctr, Dept Integrated Med, Div Nephrol, 1-847 Amanuma, Omiya, Saitama 3308503, Japan
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; MESOTHELIAL CELLS; CIRCULATING MICRORNAS; MOUSE MODEL; PATHOPHYSIOLOGY; METHYLGLYOXAL; BIOMARKERS; MEMBRANE; PROGRESSION; MATRIX;
D O I
10.1016/j.trsl.2015.10.009
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Peritoneal fibrosis (PF) is an intractable complication leading to peritoneal membrane failure in peritoneal dialysis (PD). The aim of this study was to identify microRNAs (miRNAs) involved in PF. Peritoneal tissue from a PF rat model was screened for miRNA expression using microarray analysis. The expression levels of differentially expressed miRNAs were evaluated in serum and drained dialysate and associated with peritoneal membrane functions, as measured by the peritoneal equilibrium test in 33 PD patients. Furthermore, an miRNA inhibitor (anti-miRNA-21-5p locked nucleic acid (LNA): anti-miRNA-21-LNA) was intraperitoneally injected to PF model mice to investigate its effects on PF. The initial profiling study of PF rat peritoneal tissue identified 6 miRNAs (miRNA-142-3p, miRNA-21-5p, miRNA-221-3p, miRNA-223-3p, miRNA-34a-5p, and miRNA-327) whose expression was increased more than 2-fold and no miRNAs whose expression was decreased more than half. Among them, serum levels of miRNA-21-5p, miRNA-221-3p, and miRNA-327 and drained dialysate levels of miRNA-221-3p and miRNA-34a-5p were significantly correlated with peritoneal membrane functions in PD patients. Anti-miRNA-21-LNA significantly inhibited miRNA-21-5p expression in the PF mouse peritoneum, inhibited peritoneal fibrous thickening, and maintained peritoneal membrane functions. These results suggest that several miRNAs are involved in PF and that they may be useful as novel diagnostic biomarkers and therapeutic targets for PF.
引用
收藏
页码:47 / 66
页数:20
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