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MicroRNA exocytosis by large dense-core vesicle fusion


Neurotransmitters and peptide hormones are secreted into outside the cell by a vesicle fusion process. Although non-coding RNA (ncRNA) that include microRNA (miRNA) regulates gene expression inside the cell where they are transcribed, extracellular miRNA has been recently discovered outside the cells, proposing that miRNA might be released to participate in cell-to-cell communication. Despite its importance of extracellular miRNA, the molecular mechanisms by which miRNA can be stored in vesicles and released by vesicle fusion remain enigmatic. Using next-generation sequencing, vesicle purification techniques, and synthetic neurotransmission, we observe that large dense-core vesicles (LDCVs) contain a variety of miRNAs including miR-375. Furthermore, miRNA exocytosis is mediated by the SNARE complex and accelerated by Ca2+. Our results suggest that miRNA can be a novel neuromodulator that can be stored in vesicles and released by vesicle fusion together with classical neurotransmitters.


Non-coding RNA (ncRNA) is transcribed from the genome, but not translated into a protein. The protein-coding genes occupy 1.2% of the euchromatic genome1, whereas the non-coding genes cover 60% of the genome2. Approximately 98% of RNA transcripts are non-coding2. The main functions of ncRNAs are linked to translation, RNA splicing, and gene regulation3. MicroRNAs (miRNAs) are ncRNAs with 20~24 nucleotides in length; they are involved in a variety of cellular functions4, including gene expression and cellular communication5. miRNAs associate with the complementary sequences in target mRNAs6, and thereby repress mRNA translation.

Although miRNAs are present inside the cell where miRNAs are transcribed, miRNAs can be detected outside the cells, called extracellular miRNA7,8. They participate in cell-to-cell communication9. Extracellular miRNAs have been hypothesized to be incorporated in secretory vesicles such as exosomes, microvesicles, and apoptotic bodies10, although the copy number is <111. Vesicle-free extracellular miRNAs are also detected in complexes with high-density lipoproteins (HDL)12 or Argonaute 213. More surprisingly, miRNAs seem to be released by active exocytosis in neurons14,15,16 and regulate pain signaling17. miRNAs including miR-29a and miR-125a can be secreted from synapses in a Ca2+-dependent manner14. Despite the increasing interest in extracellular miRNAs outside the neurons, little is known about the molecular mechanisms by which miRNAs can be released.

Neurons have two different types of vesicles that release neurotransmitters: synaptic vesicles and large dense-core vesicles (LDCV)18,19. LDCVs are responsible for exocytosis of amines, neuropeptides, and hormones that mainly stimulate G-protein-coupled receptors (GPCRs)18,19,20. LDCVs, also called chromaffin granules, in chromaffin cells have been used as the model system for LDCVs21. LDCVs and synaptic vesicles share the conserved fusion machinery; i.e., soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) proteins and Ca2+ sensor synaptotagmin-1 that mediates Ca2+-dependent exocytosis22.

To study miRNA exocytosis by vesicle fusion, we focus on LDCVs because of their large size, high yield, and high purity. We purified LDCVs (95% purity) from bovine chromaffin cells, then used next-generation sequencing (NGS) to sequence miRNAs stored in LDCVs. Synthetic neurotransmission, the in-vitro reconstitution of vesicle fusion, supported the hypothesis that miRNA exocytosis is mediated by SNARE proteins and accelerated by Ca2+. These results suggest that miRNAs may be neuromodulators stored in vesicles and released by vesicle fusion along with classical neurotransmitters.


We have established the LDCV purification technique based on continuous sucrose gradients using bovine adrenal medulla as described before23,24. Vesicle proteins are highly enriched, whereas other contaminants are mostly removed23. Mitochondria, late, lysosomes, early endosomes, endoplasmic reticulum, proteasomes, and peroxisomes are not detected in LDCV samples23. This purification process yields primarily mature LDCVs with 100~200 nm in diameter23; i.e., immature LDCVs (a marker, VAMP-4) are mostly removed.

We confirmed the enrichment of LDCVs by western blotting showing that LDCVs are highly enriched in vesicle membrane proteins (synaptotagmin-1 and synaptobrevin-2/VAMP-2), whereas exosomes and multivesicular bodies (a marker, LAMP-1) are removed during purification. (Supplementary Fig. 1). Proteomic profiling of exosomes25 and western blotting data26 reveal that exosomes are enriched with LAMP-1. Thus, our data support that miRNA-containing organelles are excluded.

To quantify the LDCV purity, we performed an overlay assay (Fig. 1a–d) in which LDCVs were immobilized on a poly-L-lysine-coated glass slides, then immunostained with an antibody against synaptobrevin-2/VAMP-2 (a marker for LDCVs, green) and DiI (a lipophilic membrane dye, red). Overlaps (yellow) in an overlay assay indicate LDCVs, whereas contaminants stain red; note that mitochondria could be minorly included in LDCV samples23. An overlay assay shows 95% purity of LDCVs (119 LDCVs from 125 samples, Fig. 1d). Size distribution of purified LDCVs with average of 135 nm determined by dynamic light scattering (Fig. 1e) correlate with electron microscopy data previously reported23.

Figure 1: High purity of LDCVs.
figure 1

(a) Schematic of the overlay assay for the LDCV purity. (b,c) LDCVs were incubated simultaneously with VAMP-2 antibody (green, left) and a membrane dye, DiI (red, middle). Overlay (yellow, right) indicates LDCVs (arrows). Scale bar, 2 μm. (c) High-magnification images of LDCVs stained with VAMP-2 antibody and DiI. (d) LDCV purity was presented as a percentage of LDCVs (yellow from panel b,c, n = 119) among total vesicles (red in overlay from panel b,c, n = 125). Total vesicles were collected from three independent purifications. The purity of LDCVs is 95%. (e) Size distribution of LDCVs analyzed using dynamic light scattering. Number distribution is presented as a percentage.

Next, total RNAs were extracted from purified LDCVs by using miRNeasy Mini Kit (Qiagen). The RNAs stored in LDCVs were <100 nucleotides (nt) long (Fig. 2a); rRNA was not detected, although it constitutes ~80% of the total RNA in a cell, suggesting that LDCVs are specifically enriched with small RNAs. The small RNA libraries (Supplementary Fig. 2) were read using small RNA-sequencing (RNA-seq) technique with Illumina Hiseq 2500 platform. Surprisingly, the RNA library provides evidence for miRNA fraction at the peak with 141 bp; miRNAs of 20~24 nt are conjugated to ~120 bp of adapter (Supplementary Fig. 2). miRNA fraction constitutes ~61% of RNAs extracted from LDCVs; i.e., miRNAs are selectively accumulated in LDCVs (Fig. 2b). Size selection of miRNA fraction was applied for miRNA sequencing and we found a variety of miRNAs including 459 of known miRNAs and 315 of novel miRNAs predicted by miRDeep2 analysis tool (Fig. 2c) (Supplementary Files 1 and 2). However, most of the known miRNAs were expressed at low level less than 10 (on a log2 scale) of library size normalized Count Per Million (CPM) (Fig. 2d). Therefore, we used a criterion of 1,000 CPM (9.96 on a log2 scale) to categorize miRNAs as high (69 miRNAs, 16.2%) and low (356 miRNAs, 83.8%) level miRNA (Fig. 2e,f). Intriguingly, the 69 high level miRNAs (Fig. 2e) comprise 94.8% of total mapped read counts (Fig. 2f); i.e., only a few miRNAs are highly expressed in LDCVs. miR-375 was the most abundant miRNA in LDCVs (28.9% of total mapped read counts, Fig. 2g). The most abundant miRNAs (top 5%; 21 miRNAs among 425 total miRNAs) stored in LDCVs account for 80% of CPM (Table 1). We confirmed the reproducibility of RNA-seq data by using technical and biological replicate which are highly correlated (r = 0.99, p < 0.05) (Supplementary Fig. 3). These data provide evidence that miRNAs including miR-375 are highly enriched in LDCVs.

Figure 2: Next generation sequencing for miRNAs.
figure 2

(a) Total RNA extracted from LDCVs was analyzed by electrophoresis on a 2% agarose gel. (b) Size distribution of the small RNAs. Values were calculated as a percentage based on results of electropherogram trace of total RNA libraries in the Supplementary Fig. 2. (c) Known miRNA and novel miRNA based on the number of miRNAs from RNA-seq. (d) Distribution of the number of miRNAs based on read counts; count per million (CPM) on a log2 scale. Number of known miRNAs in each CPM (log2) range is presented. (e,f) Classification of the number of miRNAs as high level (69 miRNAs) and low level (356 miRNAs) based on read counts; 1,000 CPM was applied for this classification after cut-off of <1log2 CPM (e). (f) High-level and low level-miRNAs were presented as a percentage of read counts, CPM. (g) Distribution of the most abundant miRNAs based on CPM.

Table 1 Top 5% of the most abundantly expressed known miRNAs stored in LDCVs.

Can miRNAs stored in LDCVs be released to extracellular fluid? We attempted to confirm miRNA exocytosis by using the reconstitution system of vesicle fusion called synthetic neurotransmission. We used purified LDCVs for synthetic neurotransmission and prepared plasma membrane-mimicking liposomes that contain the stabilized Q-SNARE complex (Online Methods). Liposomes also incorporated GelGreen dye, a water-soluble and membrane-impermeable green fluorescent nucleic acid dye. As a content-mixing assay, miRNAs stored in LDCVs bind to GelGreen after LDCV fusion, thereby increasing fluorescence of GelGreen (Fig. 3a). Indeed, we observed miRNA exocytosis mediated by SNARE assembly, because soluble VAMP-2 or no SNARE proteins in plasma membrane-mimicking liposomes completely inhibited miRNA exocytosis (Fig. 3b). 100 μM Ca2+ accelerated miRNA exocytosis that resulted from the activity of synaptotagmin-1, a Ca2+ sensor, for vesicle fusion (Fig. 3b, Supplementary Fig. 4). To further validate that miR-375 can be released from cells in response to stimulation, we used PC12 cell, the cell line derived from a pheochromocytoma of chromaffin cells. Indeed, stimulation of PC12 cells with 50 mM KCl that evokes membrane depolarization and Ca2+ influx increased the level of miR-375 in the extracellular (Fig. 3c), supporting miR-375 exocytosis by vesicle fusion in the physiological conditions.

Figure 3: miRNA exocytosis by vesicle fusion.
figure 3

(a) Schematic for fusion assay. Fusion was monitored using a content-mixing assay in which GelGreen, a water-soluble and membrane-impermeable nucleic acid dye, was incorporated in liposomes. Interaction of miRNA stored in LDCVs with GelGreen increases its fluorescence. Plasma membrane-mimicking liposomes incorporated the stabilized Q-SNARE complex47. VAMP-2 fragment is omitted for clarity. (b) Preincubation of liposomes with a soluble fragment of VAMP-2 (VAMP-21-96), inhibits SNARE-mediated fusion due to competitive inhibition24,51. Control, basal fusion of LDCVs with liposomes that contain Q-SNARE. No Q-SNARE, no SNAREs incorporated in liposomes. Fluorescence intensity is normalized to the initial value (F0). (c) miR-375 exocytosis from PC12 cells. PC12 cells were stimulated with 50 mM KCl for 5 min. miR-375 released by PC12 cells in the absence or presence of KCl was analyzed using qRT-PCR. Quantitative analysis was presented as fold changes in expression relative to a control (no KCl). Data are mean ± SD (n = 4 biological and technical replicates). **p = 0.0026 (two-tailed unpaired Student’s t test).

Next, we quantified the copy number of miR-375 per LDCV (Fig. 4a,b). The number of LDCV particles was measured using Nanoparticle Tracking Analysis (NTA). To determine the copy number of miR-375, which is the most abundant miRNA in LDCVs, we used quantitative real-time PCR (qRT-PCR) to quantify miR-375. A synthesized Caenorhabditis elegans microRNA (cel-miR-39) as the spike-in control was added to normalize the RNA extraction efficiency. Using the data derived from the above experiments, we analyzed the relative ratio of miR-375 to LDCVs for each sample. Each LDCV contained approximately 400~500 miR-375 (Fig. 4b), suggesting that LDCVs contain much higher number of miRNAs than other miRNA-containing organelles such as exosomes11.

Figure 4: miR-375 stored in LDCVs.
figure 4

(a,b) Quantification of miRNA copy number per LDCV. (a) Workflow to determine miRNA copy number. Aliquots of LDCVs were counted using Nanoparticle Tracking Analysis (NTA). In parallel, the concentration of miRNA extracted from LDCVs was determined by qRT-PCR. A synthesized Caenorhabditis elegans microRNA (cel-miR-39) as the spike-in control was added to normalize the RNA extraction efficiency. (b) Copy number of miR-375 per LDCV. Line represents mean (n = 4 biological and technical replicates). (c) Schematic for confirming vesicle-incorporated miR-375. cel-miR-39 was mixed with LDCVs prior to RNase A treatment. (d) Relative levels of cel-miR-39 and miR-375 with or without RNase A were determined by qRT-PCR. Values represent fold changes in expression relative to a control (no RNase A). *p = 0.014 (two-tailed unpaired Student’s t test). (e) miR-375 from purified synaptic vesicles from mice brains was analyzed by qRT-PCR. Data in d and e are mean ± SD (n = 3 technical replicates).

Can miR-375 be a contaminant from the cytosol, which is adsorbed to the outside of LDCVs during purification procedure? Next, we assessed the possibility that miR-375 could attach to vesicle membranes during the purification process as an artefact (Fig. 4c,d). To confirm that miR-375 is really stored inside LDCVs, we applied RNase A, because RNase A selectively degrades vesicle-free miRNA, but not vesicle-incorporated miRNA. Indeed, RNase A degraded cel-miR-39, which was mixed with LDCVs prior to RNase A, whereas miR-375 was intact (Fig. 4d), indicating that miR-375 is incorporated in LDCVs. Taken together, our data suggest that miR-375 is stored in LDCVs (~500 copies) and miRNA exocytosis is mediated by SNARE assembly and accelerated by Ca2+ stimulus.

Finally, we tested the specificity of miR-375 by investigating whether miR-375 is present in synaptic vesicles purified from mice brains (Fig. 4e). Surprisingly, we found that miR-375 is only stored in LDCVs, but not in synaptic vesicles, supporting the specificity of miR-375. Altogether, these data provide evidence that miR-375 is not an artefact or a byproduct caused by vesicle purification procedure, but miR-375 might be a novel neuromodulator stored in LDCVs and released by vesicle fusion in response to stimulation.


Our data strongly suggest that miRNAs are stored in vesicles and can be released along with classical neurotransmitters by vesicle fusion. LDCVs contain non-coding RNA (ncRNA) together with catecholamines. Exosomes also carry ncRNAs, but up to 90% of these are rRNAs and miRNAs are less than 5%27. Furthermore, abundant miRNAs are present at less than one copy per exosome11. In comparison with exosomes, the variety of miRNAs is highly enriched in LDCVs excluding other types of ncRNA such as rRNAs and tRNAs. These observation suggests that LDCVs may be specific cargos and carriers in neurons and neuroendocrine cells that deliver miRNAs to extracellular fluid.

The average diameter of LDCVs is 167.7 nm23, with inner radius of 80 nm, which corresponds to 2.14 × 10–18 liter. Therefore, 400 500 copies of miR-375 in a single LDCV is a concentration of 320 400 μM. LDCV in chromaffin cells contains 2.5 × 106 catecholamine molecules per vesicle28 and a variety of neuropeptides; e.g., 430 neuropeptide Y (NPY) molecules21,29. Therefore, the observed miRNA concentration is comparable to the number of other neuropeptides in LDCVs, proposing that miRNAs might be novel neuromodulators or hormones that are stored in LDCVs and released together with catecholamines and neuropeptides (Fig. 5). Therefore, we propose a new function of non-coding RNAs named ‘ribomone (ribonucleotide + hormone)’ that are stored inside the vesicles and released by active vesicle fusion in response to stimulation, thereby regulating cell-to-cell communication including gene silencing and cellular signaling.

Figure 5: A schematic summarizing miRNA exocytosis by vesicle fusion.
figure 5

LDCVs contain catecholamines that include dopamine, adrenaline, and noradrenaline, but they also contain a variety of miRNAs including miR-375. miRNA exocytosis is mediated by the SNARE complex and accelerated by Ca2+ stimulus. Released extracellular miRNAs regulate cell-to-cell communication by controlling gene silencing in target cells after endocytosis and by stimulating receptors or ion channels, thereby leading to cellular signaling. Our data suggest the new concept that miRNAs are stored in vesicles together with classical neurotransmitters and are released by vesicle fusion, thus contributing to cell-to-cell communication as a novel neuromodulator.

Extracellular circulating miRNAs have been detected in serum, so they might be biomarkers of diseases10,30,31. Most studies have proposed that extracellular miRNAs can be packaged into membrane-associated organelles such as exosomes, microvesicles, and extracellular vesicles10,32, but the mechanisms and origins of vesicle-free extracellular miRNAs remain unclear. To our knowledge, our data are the first to identify miRNA exocytosis by LDCV fusion. LDCVs in chromaffin cells, which are neuroendocrine and modified sympathetic ganglion cells, mainly contain catecholamines33. Upon activation of the sympathetic nervous system, catecholamines released by LDCV fusion spread through the bloodstream, thereby mediating stress and the ‘fight-or-flight’ physiological response33. Therefore, fusion of LDCVs could result in a high level of vesicle-free miRNAs together with catecholamines in blood.

miR-375 is the most abundant miRNA in LDCVs (~30% of total miRNA read counts); it is highly expressed in the pancreatic islets34 and motor neurons35, where it regulates neuronal development36. miR-375 is also detected in plasma and serum as a circulating miRNA, and may be a biomarker for diabetes37, hepatocellular carcinoma38, and Alzheimer’s disease39. Despite intense study of miR-375, the physiological roles and origin of circulating extracellular miR-375 are still not understood. Our data support the hypothesis that LDCVs in chromaffin cell may be one source of circulating miR-375, but its function remains to be elucidated in both normal physiological and pathological conditions.

Besides miR-375, LDCVs are enriched with miR-7, miR-103, and miR-125b, which are highly expressed in the brains40,41. miR-7 regulates neuronal development42 and miR-125b promotes neuronal differentiation43. miR-29a and miR-125a are secreted from synaptosomes in response to depolarization14, and both miR-29a and miR-125a were among the 10% of the most abundant miRNAs in LDCVs (Supplementary File 3). Another miRNA, let-7b, is released from dorsal root ganglion (DRG) neurons by depolarization and extracellular let-7b activates toll-like receptor-7 (TLR7)/TRPA1 ion channel to mediate pain signaling17. let-7b was among the 15% most-abundant miRNAs in LDCVs (Supplementary File 3).

We have essential open questions. First, what are miRNAs doing after release and what is the physiological significance? Extracellular circulating miRNAs are aberrantly detected in blood plasma and serum7,8, probably regulating cell-to-cell communication9. Extracellular miRNAs could be transported by endocytosis into the target cells, where they regulate gene expression, but the identity of the target cells and the mechanisms of endocytosis are not fully understood. Secondly, miRNA clearly regulates gene expression inside the cell, but we hypothesize that extracellular miRNAs may directly regulate receptor activity as an agonist or antagonist, similarly to aptamers, which are oligonucleotides that bind to a specific target, in a manner that differs from the way in which it regulates gene expression (Fig. 5). For example, extracellular let-7b miRNA activates TLR7 to mediate pain signaling17. So far, little is known about the signaling mechanism by which extracellular miRNAs can regulate receptors and ion channels. Thirdly, the mechanism by which miRNAs are transported into vesicles is not known. Considering that some miRNAs (e.g., miR-375) are selectively and specifically accumulated in LDCVs, LDCVs could have a carrier or transporter for miRNA uptake. LDCVs express nucleotide transporters44, but the activity of RNA uptake has never been studied. Fourthly, ribonucleases in the extracellular could degrade vesicle-free extracellular miRNAs. High-density lipoproteins (HDL)12 or Argonaute 213 might protect extracellular miRNAs from cleavage by ribonucleases. We have the mass spectrometry data showing that RNA-binding proteins such as hnRNPs and apolipoprotein A-I are detected in LDCVs whereas Argonaute 2 is not (unpublished data). Further work will be required to identify miRNA-binding proteins that control the miRNA stability and miRNA function in LDCVs.



Poly-L-lysine was from sigma (Cat: P8920) and DiIC18 was purchased from Invitrogen (Cat: D-12730, Disulfonic Acid). Monoclonal mouse antibody against synaptobrevin-2/VAMP-2 (clone, 69.1) and synaptotagmin-1 (clone, 41.1) were obtained from Synaptic Systems (Göttingen, Germany). LAMP-1 (Abcam, cat. no. ab24170) and Goat Anti-Mouse IgG (Cy2) (ab6944) was obtained from Abcam (Cambridge, UK). DC (detergent compatible) protein assay was obtained from Bio-Rad (DC Protein Assay, Cat: 5000112). GelGreen was purchased from Biotium (Hayward, CA, Cat: 41005). Nucleospin RNA plus for total RNA extraction was obtained from MACHEREY-NAGEL (Düren, Germany, Cat: 740984).

Purification of large dense-core vesicles (LDCVs) and synaptic vesicle

LDCVs were purified using a previously-reported method45 with several modifications23. Fresh bovine adrenal glands were obtained from a local slaughterhouse. The cortex and fat were removed, then the medullae were minced using scissors, then homogenized in a cooled glass-teflon homogeniser. Crude LDCV fraction was resuspended in 300 mM sucrose buffer and loaded on top of a continuous sucrose gradient (from 300 mM to 2.0 M) to remove other contaminants including mitochondria. LDCVs were collected from the pellet after centrifugation at 110,000 g for 60 min in a Beckman SW 41 Ti rotor and resuspended with the buffer (120 mM K-glutamate, 20 mM K-acetate, 20 mM HEPES.KOH, pH 7.4). Protein concentration of LDCVs were determined using a Lowry assay (Bio-Rad DC Protein Assay, Cat: 5000112). Size distribution of purified LDCVs was determined using dynamic light scattering (NanoPlus DLS, Particulate Systems).

Synaptic vesicles from mice brain were purified as described in detail elsewhere46. Briefly, mice brains were homogenized in homogenization buffer supplemented with protease inhibitors, using a glass-Teflon homogenizer. The homogenate was centrifuged for 10 min at 1,000 g and the resulting supernatant was further centrifuged for 15 min at 17,000 g. The synaptosome pellet was lysed by adding ice-cold water, followed by the centrifuge for 25 min at 48,000 g. The resulting supernatant was overlaid onto a 0.7 M sucrose cushion and centrifuged for 1 h at 133,000 g. The pellet was resuspended in the buffer (120 mM K-glutamate, 20 mM K-acetate, 20 mM HEPES.KOH, pH 7.4).

PC12 cell culture

The cells were maintained in RPMI-1640 Medium (Biochrom GmbH, Germany) containing 10% horse serum, 5% fetal bovine serum (Gibco), and 1% antibiotics (Biochrom GmbH, Germany). Cells were cultured in T-25 flask (Sarstedt, Germany) and used for experiments at 60~70% of confluency. After washing twice with PBS supplemented with 1 mM Mg2Cl and 2 mM Ca2Cl, PC12 cells were stimulated with 50 mM KCl for 5 min. Extracellular buffer was taken and subjected to qRT-PCR after centrifuging at 1,200 g for 5 min to remove cell debris followed by RNA isolation.

Protein purification

All SNARE constructs were based on Rattus norvegicus sequences. The stabilized Q-SNARE acceptor complex consisting of syntaxin-1A (aa 183–288), SNAP-25A (aa 1–206, no cysteine), and a C-terminal VAMP-2 fragment (aa 49–96) was purified as described earlier23,47. The stabilized Q-SNARE complex was expressed using co-transformation24 and purified by ion-exchange chromatography on Mono Q column (GE Healthcare, Piscataway, NJ) in the presence of 50 mM n-octyl-β-D-glucoside.

Protein structures were visualized using the program PyMOL (PDB ID: 1BYN for C2A, 1K5W for C2B, 3IPD for the SNARE complex, 2KOG for VAMP-2).

Preparation of plasma membrane-mimicking liposomes

Lipid composition (molar percentages) of liposomes that contain the Q-SNARE complex consists of 45% PC (L-α-phosphatidylcholine), 15% PE (L-α-phosphatidylethanolamine), 10% PS (L-α-phosphatidylserine), 25% Chol (cholesterol), 4% PI (L-α-phosphatidylinositol), and 1% PIP2. Lipid mixture dissolved in chloroform/methanol (2:1, v/v) was dried under a gentle stream of nitrogen in the hood for 5 min, thereby giving rise to a lipid film. The lipid film was resuspended with 25 μL buffer containing 150 mM KCl, 20 mM HEPES/KOH pH 7.4, and 5% sodium cholate. In parallel, the Q-SNARE complex was resuspended in 75 μL buffer containing 150 mM KCl, 20 mM HEPES/KOH pH 7.4, and 1.5% sodium cholate. For a content-mixing assay, GelGreen, a water-soluble and membrane-impermeable nucleic acid fluorescent dye, was included in buffer in 1:100 dilution. The protein and lipid samples were mixed in protein-to-lipid molar ratio of 1:500 (100 μL in total), then a size exclusion column was used to remove detergent (Sephadex G50 in 150 mM KCl and 20 mM HEPES, pH 7.4). Plasma membrane-mimicking liposomes that contain the Q-SNARE complex were collected as eluted; note that plasma membrane-mimicking liposomes incorporate GelGreen dye.

LDCV fusion assay

LDCV fusion in vitro was monitored using a content-mixing assay in buffer containing 120 mM K-glutamate, 20 mM K-acetate, 20 mM HEPES-KOH (pH 7.4), 1 mM MgCl2, and 3 mM 2Na-ATP. LDCVs and plasma membrane-mimicking liposomes were incubated and interaction of miRNAs with GelGreen induced by vesicle fusion increase fluorescence of GelGreen (Ex: 495 nm/Em: 520 nm). 100 μM free Ca2+ concentrations in the presence of ATP and Mg2+ were calibrated using the Maxchelator simulation program (

Overlay assay for the LDCV purity

LDCVs (5 μg) were incubated on glasses (18 mm in diameter) coated with 0.1% poly-L-lysine for 30 min at room temperature (RT) in 150 μL buffer containing 150 mM KCl and 20 mM HEPES, pH 7.4 with KOH. After fixing LDCVs with 4% PFA (in PBS) at RT for 15 min, then PFA was removed and LDCVs were washed three times with PBS. Monoclonal mouse antibody against synaptobrevin-2/VAMP-2 (Synaptic Systems; clone, 69.1) was incubated for 30 min at RT and then Cy2-linked goat anti-mouse IgG (Ex/Em: 489/505 nm) was incubated for 30 min at RT. LDCVs were simultaneously incubated with 1 μM DiI (Ex/Em: 549/565 nm) with VAMP-2 antibody. DiI stains membranes of LDCVs and other contaminant organelles. The two channels (green and red) constitute an overlay images through direct observation in a microscope. The LDCV purity was presented as the percentage of the number of LDCVs from the organelles counted (n = 125).

RNA-seq data

RNA sequencing (RNA-seq) was performed by Gene Core Sequencing Facility (EMBL, using Illumina Hiseq 2500. Briefly, total RNA (1 μg) was extracted from 300 μg of purified LDCVs by using miRNeasy Mini Kit (Qiagen, Cat: 217004). Then, the small RNA libraries have been prepared starting with 500 ng of RNA using the NEBNext® Multiplex Small RNA Library Prep Set for Illumina® (Set 1) (NEB, Cat: E7300S/L). Size selection of the fraction around 140 bp (including 120 bp of adapter) was performed using a 4% Metaphor Agarose gel by Lonza (Cat: 50180). All libraries were pooled equimolar and sequenced 51 bp plus one 7 bp Index read on a Hiseq 2500 using Illumina v3 sequencing by synthesis (SBS) chemistry.

Computational analysis of RNA-sequencing data

The quality control of RNA-sequencing data set was performed using the FASTQC tool []. The mapper utility of miRDeep2 v2.0.0.748 was used to remove 3′ adapter sequences (AAGATCGGAAGAGCACACGTCT) of Illumina reads. Trimmed reads were then aligned using mapper utility to Bos taurus (UMD3.1 assembly, Ensembl release 84) reference genome with default parameters, except that the reads with <17 nucleotides were discarded. miRBase (release 21)49 and script were used to quantify expression levels of known microRNA species and to discover novel microRNA transcripts. The output of microRNA counts from script were converted to library size normalized Count Per Million (CPM) values by using the cpm function of edgeR50 Bioconductor package. miRNAs that were expressed ≥1 log2 CPM in all samples were used in further analysis.

Counting miRNA copy number and confirming vesicle-incorporated miR-375

The number of purified LDCVs was determined using Nanoparticle Tracking Analysis (NTA) (Malvern NanoSight LM10). In parallel, the concentration of miRNA extracted from LDCVs was determined using quantitative real-time PCR (qRT-PCR). A synthesized Caenorhabditis elegans microRNA (cel-miR-39) as the spike-in control was added to vesicle samples to normalize the RNA extraction efficiency. RNA was isolated using miRNeasy Mini Kit (Qiagen, Cat: 217004), then cDNA was made using miScript RT II (Qiagen, Cat: 218161) according to the manufacturer’s protocol. A serial dilution of synthetic bta-miR-375 and cel-miR-39 was used to plot a standard curve to assess absolute miRNA quantification. The primers were UUUUGUUCGUUCGGCUCGCGUGA (Qiagen Cat: MS00053865) for bta-miR-375, and UCACCGGGUGUAAAUCAGCUUG (Qiagen Cat: MS00019789) for cel-miR-39.

For confirming vesicle-incorporated miR-375, 1 pmol of cel-miR-39 was mixed with 80 μg of purified LDCVs prior to RNase A treatment (10 μg/ml, 15 min, RT). RNase A selectively degrades vesicle-free miRNA whereas vesicle-incorporated miRNA is intact. 20 units of RNase inhibitor (ribonuclease inhibitor, Thermo Fisher Scientific, Cat: N8080119) was added before RNA extraction in order to inactivate RNase. As described above, RNA was isolated using miRNeasy Mini Kit, and then levels of cel-miR-39 and miR-375 with or without RNase A were determined by qRT-PCR followed by absolute miRNA quantification.

Statistical analysis

All quantitative data are presented as means ± standard deviation (SD). Comparison between two groups were analyzed by two-tailed unpaired Student’s t-test. Statistical significance was set at p < 0.05.

Additional Information

Accession Codes: Our NGS data (RNA-Seq) have been deposited with Gene Expression Omnibus (GEO) under accession codes GSE84834, GSM2252051 (miRNAs_LDCV_technical replicate_1), GSM2252052 (miRNAs_ LDCV_technical replicate_2), and GSM2252053 (miRNAs_LDCV_biological replicate_1). The following link has been created to allow review of record GSE84834 while it remains in private status:

How to cite this article: Gümürdü, A. et al. MicroRNA exocytosis by large dense-core vesicle fusion. Sci. Rep. 7, 45661; doi: 10.1038/srep45661 (2017).

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We thank Dr. Reinhard Jahn for all constructs and samples. We are deeply indebted to Dr. Kyong-Tai Kim for technical support. We thank the Sequencing Service Gene Core Sequencing Facility (EMBL, for RNA-seq analysis. This work was supported by EMBO Installation Grant (IG Project Number 3265 to Y.P.) and 2236 Co-Funded Brain Circulation Scheme (Project Number 116C022 to Y.P.).

Author information




A.G., R.Y., and E.E. performed RNA extraction from LDCVs, synaptic vesicles, and PC12 cells. A.G., R.Y., and E.E. performed RNA preparation for NGS. A.G., R.Y., and E.E. carried out absolute miRNA quantification for counting copy number and confirming vesicle-incorporated miR-375. A.G., R.Y., and Y.P. contributed fusion assay. A.G. carried out dynamic light scattering and bioanalyzer. G.K. and T. Ü. performed computational analysis of RNA-sequencing data. Y.P. carried out LDCV purification and overlay assay. Y.P. designed, collected, and analyzed data. S.G. and Y.P. wrote the manuscript and all authors read and provided their comments on the draft. Y.P. supervised the project.

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Correspondence to Yongsoo Park.

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Gümürdü, A., Yildiz, R., Eren, E. et al. MicroRNA exocytosis by large dense-core vesicle fusion. Sci Rep 7, 45661 (2017).

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