| Literature DB >> 28715379 |
Keiji Hirai1, Hiromichi Yoshizawa2, Toshimi Imai2, Yusuke Igarashi2, Ichiro Hirahara2, Susumu Ookawara2, Kenichi Ishibashi3, Yoshiyuki Morishita4.
Abstract
MicroRNAs (miRNAs) are small noncoding RNAs that regulate messenger RNA expression post-transcriptionally. The miRNA expression profile has been investigated in various organs and tissues in rat. However, standard methods for the purification of miRNAs and detection of their expression in rat peritoneal membrane have not been well established. We have developed an effective and reliable method to purify and quantify miRNAs using quantitative real-time reverse-transcription polymerase chain reaction (qRT-PCR) in rat peritoneal membrane. This protocol consists of four steps: 1) purification of peritoneal membrane sample; 2) purification of total RNA including miRNA from peritoneal membrane sample; 3) reverse transcription of miRNA to produce cDNA; and 4) qRT-PCR to detect miRNA expression. Using this protocol, we successfully determined that the expression of six miRNAs (miRNA-142-3p, miRNA-21-5p, miRNA-221-3p, miRNA-223-3p, miRNA-327, and miRNA-34a-5p) increased significantly in the peritoneal membrane of a rat peritoneal fibrosis model compared with those in control groups. This protocol can be used to study the profile of miRNA expression in the peritoneal membrane of rats in many pathological conditions.Entities:
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Year: 2017 PMID: 28715379 PMCID: PMC5608527 DOI: 10.3791/55505
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355