| Literature DB >> 26004781 |
Kenji Miki1, Kei Endo2, Seiya Takahashi3, Shunsuke Funakoshi4, Ikue Takei3, Shota Katayama3, Taro Toyoda3, Maki Kotaka3, Tadashi Takaki3, Masayuki Umeda5, Chikako Okubo3, Misato Nishikawa3, Akiko Oishi3, Megumi Narita3, Ito Miyashita3, Kanako Asano3, Karin Hayashi3, Kenji Osafune3, Shinya Yamanaka6, Hirohide Saito7, Yoshinori Yoshida8.
Abstract
Isolation of specific cell types, including pluripotent stem cell (PSC)-derived populations, is frequently accomplished using cell surface antigens expressed by the cells of interest. However, specific antigens for many cell types have not been identified, making their isolation difficult. Here, we describe an efficient method for purifying cells based on endogenous miRNA activity. We designed synthetic mRNAs encoding a fluorescent protein tagged with sequences targeted by miRNAs expressed by the cells of interest. These miRNA switches control their translation levels by sensing miRNA activities. Several miRNA switches (miR-1-, miR-208a-, and miR-499a-5p-switches) efficiently purified cardiomyocytes differentiated from human PSCs, and switches encoding the apoptosis inducer Bim enriched for cardiomyocytes without cell sorting. This approach is generally applicable, as miR-126-, miR-122-5p-, and miR-375-switches purified endothelial cells, hepatocytes, and insulin-producing cells differentiated from hPSCs, respectively. Thus, miRNA switches can purify cell populations for which other isolation strategies are unavailable.Entities:
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Year: 2015 PMID: 26004781 DOI: 10.1016/j.stem.2015.04.005
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633