Long non-coding RNAs with low expression levels in cells are enriched in secreted exosomes - PubMed (original) (raw)
doi: 10.1002/cbin.10301. Epub 2014 May 13.
Affiliations
- PMID: 24798520
- DOI: 10.1002/cbin.10301
Long non-coding RNAs with low expression levels in cells are enriched in secreted exosomes
Ugur Gezer et al. Cell Biol Int. 2014 Sep.
Abstract
Long non-coding RNAs (lncRNAs) are involved in regulating chromatin modifications, gene transcription, mRNA translation, and protein function. We recently reported a high variation in the basal expression levels of a panel of lncRNAs in HeLa and MCF-7 cells and their differential response to DNA damage induction. Here, we hypothesized that lncRNA molecules with different cellular expression may have a differential abundance in secreted exosomes, and their exosome levels would reflect cellular response to DNA damage. MALAT1, HOTAIR, lincRNA-p21, GAS5, TUG1, CCND1-ncRNA in exosomes secreted from cultured cells were characterized. A different expression pattern of lncRNAs in exosomes was seen compared to cells. RNA molecules with relative low expression levels (lincRNA-p21, HOTAIR, ncRNA-CCND1) were highly enriched in exosomes. TUG1 and GAS5 levels were moderately elevated in exosomes, whereas MALAT1--which was the most abundant molecule in cells--was present at levels comparable to its cellular levels. lincRNA-p21 and ncRNA-CCND1 were the main molecules; exosome levels of them best reflect the change of their cellular levels upon exposure of the cells to bleomycin-induced DNA damage. In conclusion, we provide evidence that lncRNAs have a differential abundance in exosomes, indicating a selective loading.
Keywords: HeLa cells; MCF-7 cells; exosomes; long noncoding RNAs.
© 2014 International Federation for Cell Biology.
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