1. Introduction
Mesenchymal stromal cells (MSCs) are one of the most studied adult stem cells and have been extensively applied in the field of regenerative medicine. In the last years, many studies have demonstrated that their therapeutic effects are mainly mediated by the secretion of bioactive molecules (such as RNAs, proteins, and lipids) that can be directly released in the local microenvironment or packaged in extracellular vesicles (EVs) [
1]. Paracrine factors released by MSCs, including EVs, induce the recovery of injured tissue and modulate the immune response and inflammation [
2,
3]. Many reports have demonstrated the application of MSCs and of their derived EVs in the recovery of renal dysfunction [
4]. Different preclinical models of acute and chronic kidney injuries have been used to demonstrate the efficacy of EVs from MSCs in the amelioration of acute kidney injury (AKI) and in preventing progression at the chronic stage [
5]. Recently, we tested different subpopulations of MSC-derived EVs in renal regeneration. Most of the effects observed in the recovery from AKI were ascribed to the exosomal fraction, which carried mRNA, miRNAs and proteins that induced the proliferation of tubular cells. Despite the inefficiency of the non-exosomal fraction, we observed that the effect of the exosomal fraction and the total-EVs was not significantly different in terms of pro-regenerative potential, suggesting that the ineffective fraction did not interfere with the exosomal fraction activity [
6]. Moreover, MSCs may be manipulated in culture by transferring specific miRNA to EV-producing cells to obtain modified-EVs with potentiated pro-regenerative or reparative effects [
7,
8,
9,
10,
11]. In this work, we set up a method to increase—in MSCs and in their total-EVs—the content of specific miRNAs involved in renal regeneration. To assess the capacities of modified-EVs to contribute to AKI recovery, we tested them in vitro on murine renal tubular epithelial cells and in vivo in a model of AKI induced by glycerol injection.
3. Discussion
Recent studies have shown that paracrine mechanisms, including EVs, are responsible for stem/progenitor cell-mediated renal regenerative effect [
5]. EVs derived from MSCs shuttle different molecules (proteins, lipids, and nucleic acids) that may contribute to their pro-regenerative potential. Among the different shuttled molecules, miRNAs have been reported to be one of the factors involved in the pro-regenerative effects of MSC-EVs. Indeed, miRNA deregulation by Drosha-knockdown in MSCs has been reported to inhibit the regenerative potential of MSCs and of their derived EVs in a murine model of AKI [
12]. This suggests a critical role of miRNA content in MSCs and MSC-EVs in the recovery following an AKI.
The idea of using EVs as carriers for selected miRNA cargo became very attractive in the last decades. EVs overcome many problems related to stability and preservation of their cargo from degradation in circulation. Different approaches were developed in order to modify EV content to enhance their homing capacity (proteins) or their effect (miRNAs, mRNAs and drugs) [
13]. Direct manipulation of EVs implies the temporary disruption of EV membranes by different techniques, such as electroporation, sonication or chemical transfection [
14]. Another technique used to enhance miRNA content in EVs is engineering of the parental cells. Some recent works demonstrated that is possible to load miRNA mimic or antimiR into MSCs by transfection, as well as to increase the pro-regenerative properties of EVs in different tissue injuries [
7,
8,
9,
10,
11,
15] or to potentiate their anti-tumor effect [
16,
17].
In this study, we set up a method to increase the content of specific miRNAs involved in renal regeneration in MSCs and their respective EVs. Potentially regenerative miRNAs were selected using a bio-informatic approach based on predicted interactions between the miRNAs present inside the MSC-EVs with genes modulated during AKI treatment with MSC-EVs. Moreover, this list was implemented with miR-486-5p, which was highly expressed in the exosomal fraction of MSC-EVs [
6]. Of relevance, miR-486-5p and some of the miRNAs selected by bio-informatic analyses (miR-10a-5p, miR-29a-3p) were found to be down-regulated in EVs obtained by Drosha knock-down MSCs, which were ineffective in glycerol induced AKI [
12].
In this work, we demonstrated that the miRNA mimics transfected in MSCs were also up-regulated in their EVs. Among the different miRNA mimics transfected, miR-127 and miR-486 were more enriched than miR-29a in cells and, consequently, in their EVs, suggesting differences in efficiency of transfection for different miRNAs.
The EVs obtained from transfected cells with miR-10a, -127 and -486 were tested in vivo. Treatment with a dose of miRNA-enriched EVs known to be effective in the AKI model [
6] did not provide any significant improvement, while a worsening was observed for miR-10a- and miR-486-enriched EVs. These data suggest that changing the miRNA composition of MSC-EVs can alter their renal regenerative capacities. When we used an ineffective dose of naïve-EVs as the control, and a similar dose miR-10a- and miR-486-enriched EVs, a significant improvement of renal function and morphology was invariably observed. These findings indicate that in order to detect biological activity of miRNA-enriched EVs, low doses of EV should be studied. Moreover, these data highlight the important role of miR-10a and of miR-486 in the pro-regenerative effect exerted by MSC-EVs in AKI. Interestingly, miR-486 is also in exosomes derived from human endothelial progenitor cells, which have been shown to possess renal regenerative capacity in ischemia-reperfusion injury models [
18].
In conclusion, our study has demonstrated that it is possible to modify the miRNA content of MSCs and their EVs. Changing the amount of pro-regenerative miRNAs in EVs was found to modify the window of biological activity of these EVs. Therefore, this may be a strategy to reduce the amount of EVs used in therapy. We previously showed that EVs derived from MSCs accumulated specifically in the kidneys of mice with AKI compared to healthy controls [
19]. Since in the present study the bio-distribution of miRNA-enriched EVs was not evaluated, we cannot rule out the possibility that miRNA-enriched EVs have a different bio-distribution.
4. Materials and Methods
4.1. Cell Cultures and EV-CTRL Isolation
Bone marrow MSCs were purchased from Lonza (Basel, Switzerland) and cultured in a mesenchymal stem cells basal medium bullet kit (Lonza). MSCs were used for the different experiments until passage 6 and expressed the typical MSC markers (CD105, CD29, CD73, CD44 and CD90) (not shown).
MSC-EVs, used as control (EV-CTRL), were obtained by ultracentrifugation, as described in Reference [
6]. Briefly, EVs were obtained from supernatants of MSCs cultured overnight in (Roswell Park Memorial Institute (RPMI) medium. After removal of cell debris and apoptotic bodies by centrifugation at 3000×
g for 20 min, EVs were purified by 2 h ultracentrifugation at 100,000×
g at 4 °C. EVs from control MSCs or from modified MSCs were used freshly or stored at −80 °C after resuspension in RPMI supplemented with 1% dimethyl sulfoxide (DMSO, Sigma, St. Louis, MO, USA).
Murine renal tubular epithelial cells (mTECs) were obtained as previously described [
20] and cultured in Dulbecco’s Modified Eagle Medium (DMEM) low glucose (Euroclone, Pero, Italy) supplemented with 10% fetal calf serum (FCS, Euroclone), penicillin (50 IU/mL), and streptomycin (50 µg/mL) (Sigma). Murine TECs were characterized for positive staining to cytokeratin, alkaline phosphatase and aminopeptidase A, and for negative staining for endothelial (von Willebrand factor), hematopoietic (CD45) and glomerular (nephrin) markers.
4.2. MSC Transfection and Collection of Engineered MSC-EVs
To obtain miRNA-enriched MSCs, cells were transiently transfected by electroporation (MSC-EP) (neon transfection system) using a 100 µl tip (Thermo Fisher Scientific, Waltham, MA, USA), according to the manufacturer’s protocol. Different electroporation conditions with a control miRNA mimic (100 nM) were tested in order to find the optimal protocol (
Table 2 and
Figure 2A). The electroporation conditions were set to 990 V, 40 msec and 1 pulse (EP1 protocol).
Three different doses (5, 25 and 50 nmol /4 × 10
4 cells) of a control miRNA mimic were evaluated to find the optimal dose to transfect MSCs (
Figure 2B). The dose 25 nmol/4 × 10
4 cells was selected for subsequent experiments. The transfection efficiency was evaluated by qRT-PCR with the miScript PCR system (Qiagen, Venlo, The Netherlands), following the manufacturer’s protocol.
These electroporation conditions did not affect cell viability (not shown).
Selected miRNA mimics (hsa-miR-10a-5p, hsa-miR-29a-3p, hsa-miR-127-3p, hsa-miR-486-5p) (Qiagen) were used to enrich MSCs (600 pmol/106 cells). As a control, MSCs were transfected with AllStars Negative Control siRNA (SCR-Qiagen) and used for normalization of transfection with different mimics. For modified MSCs, EV collection was carried out starting from a four sub-confluent flask (T75, Euroclone S.p.A) 24 h after the electroporation, starving MSCs over-night in RPMI (Euroclone). The collected medium was centrifuged at 2000 g for 20 min to eliminate cell debris. Supernatant was then micro-filtrated and concentrated by an Amicon® Ultra 15 mL 3 kDa cut off filter (Merck-Millipore, Darnstadt, Germany) at 4000 rpm 60 min at 4 °C. EV samples were stored at −80 °C, with addition of 1% DMSO (Sigma).
4.3. EV Characterization
Analysis of size distribution and enumeration of EVs from naïve MSCs and from MSC-EP (enriched or not with specific miRNA mimics) were performed using NanoSight NS300 (NanoSight Ltd., Amesbury, UK) equipped with a 405 nm laser and nanoparticle tracking analysis (NTA) 3.2 software, as described in Reference [
6]. Using a laser light source, particles in the sample are illuminated and the scattered light is captured by the camera and displayed on a connected computer running NTA. Using NTA, the particles are automatically tracked and sized based on Brownian motion and the diffusion coefficient. Three videos of 30 s were recorded to perform the analyses.
EV-surface expression markers were analyzed by Guava easyCyte™ Flow Cytometer (Millipore), as previously described [
21]. FITC-, PE- or APC-conjugated antibodies against CD44, CD29, CD73 and CD63 (all from Miltenyi Biotec GmbH, Bergisch Gladbach, Germany) were employed. Isotopic IgG was used as the negative control. Briefly, EVs were incubated at 4 °C for 15 min with the antibodies, then diluted 1:3 and acquired immediately. Samples were acquired using a Guava easyCyte Flow Cytometer (Millipore) and analyzed with InCyte software.
Transmission electron microscopy was performed on CTRL-EVs and EV-EP placed on 200 mesh nickel formvar carbon-coated grids (Electron Microscopy Science, Hatfield, PA, USA) and left to adhere for 20 min, as described in Reference [
22]. The grids were then incubated with 2.5% glutaraldehyde containing 2% sucrose and, after washings in distilled water, the EVs were negatively stained with NanoVan (Nanoprobes, Yaphank, NK, USA) and observed using a Jeol JEM 1010 electron microscope (Jeol, Tokyo, Japan).
4.4. RNA Analysis
RNA from MSC-EP was extracted by TRIzol™ (Ambion, Thermo Fisher Scientific, Waltham, MA, USA) according to the manufacturer’s protocol.
Only for RNA analysis, Exoquick (System Biosciences, LLC, Palo Alto, CA, USA) was used to precipitate EVs obtained from MSC-EP (EV-EP), MSC transfected with scrambled siRNA (EV-SCR) or with the selected mimics (EV-miR127, EV-miR10a, EV-miR486, EV-miR29a). RNA was extracted with RNA/DNA/Protein Purification Plus Kit (Norgen Biotek Corp, Thorold, ON, Canada), following the manufacturer’s protocol.
RNA concentration was spectroscopically determined by NanoDrop2000 (Thermo Fisher Scientific). cDNA was synthetized and RT-PCR was performed by using miRCURY™ LNA™ Universal RT microRNA PCR (Exiqon-Qiagen, Vedbaek, Denmark). Specific primers set for hsa-miR-127-3p, hsa-miR-10a-5p, hsa-miR-29a-3p, hsa-miR-486-5 were used. U6 spike-in was used for housekeeping (Exiqon-Qiagen). Data were normalized with respect to MSC transfected with the SCR and were represented as relative quantification (RQ) ± SEM.
4.5. Integrating miRNA Expression in MSC EVs and RNA Analysis in AKI Animals
To identify potentially relevant miRNAs carried by MSC EVs and involved in the positive readout associated with EVs treatment, we proceeded as follows: For each miRNA family listed in TargetScan we generated a list of predicted targets. We then compared the fold-change in expression of these targets with the fold-change in expression of all the genes that were predicted targets of miRNAs but not of the miRNA families under analysis. The miRNA families selected were those for which the targets showed significant down-regulation in the kidneys of AKI mice treated with MSC-derived EVs vs. untreated AKI mice (AKI), as detected in Reference [
12]. The obtained miRNA families were then matched with the list of miRNAs detected inside the total extracellular vesicle population (100K TOT) in Reference [
6].
4.6. mTEC Proliferation Assay
mTEC were seeded in 96-well plates at a density of 1000 cells/well and maintained in a hypoxia chamber (Stem Cell Technology, Vancouver)) for 48 h with 1% O2 in DMEM + 10% FCS (positive control), DMEM + 0% FCS (negative control). During the reoxygenation step, mTEC were treated for 24 h with mimics of selected miRNAs (100 nM) or 500 EV/mTEC. Cell proliferation was assessed by a 5-bromo-2′-deoxy-uridine (BrdU) incorporation assay (Roche Applied Science, Mannheim, Germany).
4.7. SCID Mouse Model of AKI
Animal studies were conducted in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals. All procedures were approved by the Italian Health Ministry (authorization number: 211/2016-PR).
AKI was induced by an intramuscular injection (IM) of glycerol (Sigma) in SCID mice, as described previously [
6,
20]. Male SCID mice were anesthetized with an IM injection of zolazepam (80 mg/kg) and xilazina (16 mg/kg) and then injected with 8 mL/kg of 50% glycerol in water. Half the dose was injected into each muscle of the inferior hind limbs. Three days after the glycerol injection, the mice were treated intravenously with either 120 μL of the vehicle alone (
n = 7) or containing 165 × 10
6 or 82.5 × 10
6 particles of EVs derived from control MSCs (EV-CTRL,
n = 8), from MSC-EP (EV-EP,
n = 8/doses), or from EP-MSC enriched with specific miRNA mimics (EV-miR127, EV-miR486, EV-miR10a,
n = 6/group/doses). The mice were sacrificed 5 days after the glycerol injection (2 days after EV treatment).
Blood samples were collected 5 days after glycerol-induced AKI for the measurement of blood urea nitrogen (BUN) and creatinine. BUN was measured by direct quantification of serum urea with a colorimetric assay kit according to the manufacturer’s protocol (Arbor Assays, Ann Arbor, MI, USA). Serum creatinine was measured using a colorimetric microplate assay based on the kinetic Jaffe reaction as per the manufacturer’s protocol (Quantichrom Creatinine Assay; BioAssay Systems, Hayward, CA, USA).
Renal morphology was evaluated through formalin-fixed paraffin-embedded tissue staining, as previously described [
6,
20]. Briefly, 5-μm-thick paraffin kidney sections were routinely stained with hematoxylin and eosin (Merck-Millipore) for microscopic evaluation. Luminal hyaline casts and cell necrosis (denudation of the tubular basement membrane) were assessed in non-overlapping fields (10 for each section) using a 40× objective (high-power field [HPF]). The number of casts and tubular profiles showing necrosis were recorded in a single-blind manner.
4.8. Statistical Analyses
Data were analyzed using the GraphPad Prism 6.0 program. Statistical analysis was performed by employing Student’s
t-tests, analysis of variance (ANOVA) with Dunnett’s multi-comparison tests or Multiple t test with Helm–Sidak method correction as deemed appropriate. A
p-value of <0.05 was considered significant. For the bioinformatic analyses,
p values were generated by Mann–Whitney statistical test comparing the median fold change of genes down-regulated in EV treated animals (Log EV treated vs. AKI untreated) that were target of miRNAs with the non-target genes. Nine miRNA families (
Table 1) achieved nominal significance (
p < 0.05).