| Literature DB >> 32716396 |
Shohei Kaneko1, Katsunori Yanai2, Hiroki Ishii2, Akinori Aomatsu3, Kiyonori Ito2, Keiji Hirai2, Susumu Ookawara2, Kenichi Ishibashi4, Yoshiyuki Morishita2.
Abstract
Immunoglobulin A (IgA) nephropathy is a type of primary glomerulonephritis characterized by the abnormal deposition of IgA, leading to the end-stage renal failure. In recent years, the involvement of microRNAs (miRNAs) has been reported in the pathogenesis of IgA nephropathy. However, there is no established method for profiling miRNAs in IgA nephropathy using small animal models. Therefore, we developed a reliable method for analyzing miRNA in the kidney of an IgA mouse model (HIGA mouse). The goal of this protocol is to detect the altered expression levels of miRNAs in the kidneys of HIGA mice when compared with the levels in kidneys of control mice. In brief, this method consists of four steps: 1) obtaining kidney samples from HIGA mice; 2) purifying total RNA from kidney samples; 3) synthesizing complementary DNA from total RNA; and 4) quantitative reverse transcription polymerase chain reaction (qRT-PCR) of miRNAs. Using this method, we successfully detected the expression levels of several miRNAs (miR-155-5p, miR-146a-5p, and miR-21-5p) in the kidneys of HIGA mice. This new method can be applied to other studies profiling miRNAs in IgA nephropathy.Entities:
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Year: 2020 PMID: 32716396 DOI: 10.3791/61535
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355