Journal
ONCOTARGET
Volume 6, Issue 42, Pages 44745-44757Publisher
IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.6297
Keywords
microRNAs; miR-31; super-resolution; localization microscopy; metastasis
Categories
Funding
- Alfried Krupp von Bohlen und Halbach Foundation, Essen
- Dr Hella-Buehler-Foundation, Heidelberg
- Dr Ingrid-zu-Solms Foundation, Frankfurt
- Walter Schulz Foundation, Munich
- Deutsche Krebshilfe, Bonn [109558]
- DKFZ-MOST German Israel Cooperation, Heidelberg [CA149]
- HIPO/POP-Initiative for Personalized Oncology, Heidelberg [H032, H027]
- Wilhelm Sander Foundation, Munich, Germany [2012.036.1]
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We describe a novel approach for the detection of small non-coding RNAs in single cells by Single-Molecule Localization Microscopy (SMLM). We used a modified SMLM-setup and applied this instrument in a first proof-of-principle concept to human cancer cell lines. Our method is able to visualize single microRNA (miR)-molecules in fixed cells with a localization accuracy of 10-15 nm, and is able to quantify and analyse clustering and localization in particular subcellular sites, including exosomes. We compared the metastasis-site derived (SW620) and primary site derived (SW480) human colorectal cancer (CRC) cell lines, and (as a proof of principle) evaluated the metastasis relevant miR-31 as a first example. We observed that the subcellular distribution of miR-31 molecules in both cell lines was very heterogeneous with the largest subpopulation of optically acquired weakly metastatic cells characterized by a low number of miR-31 molecules, as opposed to a significantly higher number in the majority of the highly metastatic cells. Furthermore, the highly metastatic cells had significantly more miR-31-molecules in the extracellular space, which were visualized to co-localize with exosomes in significantly higher numbers. From this study, we conclude that miRs are not only aberrantly expressed and regulated, but also differentially compartmentalized in cells with different metastatic potential. Taken together, this novel approach, by providing single molecule images of miRNAs in cellulo can be used as a powerful supplementary tool in the analysis of miRNA function and behaviour and has far reaching potential in defining metastasis-critical subpopulations within a given heterogeneous cancer cell population.
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