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Journal ArticleDOI

Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells

TLDR
It is shown that exosomes contain both mRNA and microRNA, which can be delivered to another cell, and can be functional in this new location, and it is proposed that this RNA is called “exosomal shuttle RNA” (esRNA).
Abstract
Exosomes are vesicles of endocytic origin released by many cells. These vesicles can mediate communication between cells, facilitating processes such as antigen presentation. Here, we show that exosomes from a mouse and a human mast cell line (MC/9 and HMC-1, respectively), as well as primary bone marrow-derived mouse mast cells, contain RNA. Microarray assessments revealed the presence of mRNA from approximately 1300 genes, many of which are not present in the cytoplasm of the donor cell. In vitro translation proved that the exosome mRNAs were functional. Quality control RNA analysis of total RNA derived from exosomes also revealed presence of small RNAs, including microRNAs. The RNA from mast cell exosomes is transferable to other mouse and human mast cells. After transfer of mouse exosomal RNA to human mast cells, new mouse proteins were found in the recipient cells, indicating that transferred exosomal mRNA can be translated after entering another cell. In summary, we show that exosomes contain both mRNA and microRNA, which can be delivered to another cell, and can be functional in this new location. We propose that this RNA is called "exosomal shuttle RNA" (esRNA).

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Journal ArticleDOI

Sorting Mechanisms for MicroRNAs into Extracellular Vesicles and Their Associated Diseases.

TL;DR: The mechanisms whereby cells selectively sort miRNA into EVs are overviewed and disease states where EV-miRNAs become dysregulated are outlined, shedding light on the potential role of selective sorting in pathogenesis.
Journal ArticleDOI

Mesenchymal stem cell derived-exosomes: a modern approach in translational medicine.

TL;DR: In comparison with their donor cells, MSC-derived exosomes offer more stable entities and diminished safety risks regarding the administration of live cells, e.g. microvasculature occlusion risk.
Journal ArticleDOI

The exosomes in tumor immunity

TL;DR: This review focuses on exosome-mediated Immunosuppression via inhibition of antitumor responses elicited by immune cells and induction of immunosuppressive or regulatory cell populations (MDSCs, Tregs and Bregs), and the current application of DC-derived and modified tumor-derived exosomes as tumor vaccines.
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Serum microRNA-1 and microRNA-122 are prognostic markers in patients with hepatocellular carcinoma

TL;DR: The data indicate that serum miR-1 is a new independent parameter of OS in HCC patients and may therefore improve the predictive value of classical HCC staging scores.
Journal ArticleDOI

Circulating miR-30a, miR-126 and let-7b as biomarker for ischemic stroke in humans

TL;DR: Data suggest thatmiR-30a, miR-126 and let-7b might be useful biomarkers for ischemic stroke in humans.
References
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Journal ArticleDOI

Combinatorial microRNA target predictions.

TL;DR: PicTar, a computational method for identifying common targets of micro RNAs, is presented and widespread coordinate control executed by microRNAs is suggested, thus providing evidence for coordinate microRNA control in mammals.
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B lymphocytes secrete antigen-presenting vesicles.

TL;DR: It is demonstrated by immunoelectron microscopy that the limiting membrane of MIICs can fuse directly with the plasma membrane, resulting in release from the cells of internal MHC class II-containing vesicles, suggesting a role for exosomes in antigen presentation in vivo.
Journal ArticleDOI

Identification and proteomic profiling of exosomes in human urine

TL;DR: The results indicate that exosome isolation may provide an efficient first step in biomarker discovery in urine and identify numerous protein components of MVBs and of the endosomal pathway in general.
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Fate of the transferrin receptor during maturation of sheep reticulocytes in vitro: Selective externalization of the receptor

TL;DR: The fate of the transferrin receptor during in vitro maturation of sheep reticulocytes has been followed using FITC- and 125I-labeled anti-transferrin-receptor antibodies and it can be shown that at 0 degree C or in phosphate-buffered saline the rate of vesicle release is less than that at 37 degrees C in culture medium.
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Embryonic stem cell-derived microvesicles reprogram hematopoietic progenitors: evidence for horizontal transfer of mRNA and protein delivery.

TL;DR: ES-MV isolated from murine ES cells in serum-free cultures significantly enhanced survival and improved expansion of murine HPC, and upregulated the expression of early pluripotent and early hematopoietic stem cells in these cells.
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