| Literature DB >> 27523074 |
Makio Kusaoi1, Ken Yamaji1, Yusuke Ishibe1, Go Murayama1, Takuya Nemoto1, Fumio Sekiya1, Takayuki Kon1, Michihiro Ogasawara1, Kazuo Kempe1, Naoto Tamura1, Yoshinari Takasaki1.
Abstract
MicroRNAs (miRNAs), which are important inhibitors of mRNA translation, participate in differentiation, migration, cell proliferation, and cell death. The pathology of miRNAs results in alterations in protein expression. Recently, miRNAs circulating in peripheral blood have been shown to control the synthesis and translation of proteins at distal sites after intake into local cells. A number of studies are currently being conducted to investigate how to use miRNAs in disease treatment, but no studies have attempted to alleviate disease by directly eliminating miRNAs from blood. Therefore, we examined whether the removal or reduction of circulating miRNAs with apheresis improved pathologies caused by miRNAs. After approval of the study by our medical school's ethics committee, we collected blood and separated plasma samples from three patients with systemic lupus erythematosus who were undergoing plasmapheresis at our hospital. Peripheral blood was collected before and after it was passed through a primary membrane, centrifuged, and used to extract circulating miRNAs. A comprehensive expression analysis was then performed with a miRNA array chip. The levels of expression of a large number of circulating miRNAs were measured in the plasma samples separated by the primary membranes from all 3 patients with systemic lupus erythematosus. We present the first report that circulating miRNAs in peripheral blood can be separated and possibly directly removed using membrane separation apheresis.Entities:
Keywords: Circulating microRNA; Exosomes; Membrane apheresis; Microarray; Plasma; Systemic lupus erythematosus
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Year: 2016 PMID: 27523074 DOI: 10.1111/1744-9987.12471
Source DB: PubMed Journal: Ther Apher Dial ISSN: 1744-9979 Impact factor: 1.762