Exosomes derived from endometriotic stromal cells have enhanced angiogenic effects in vitro

Djana Harp, Adel Driss, Sharifeh Mehrabi, Indrajit Chowdhury, Wei Xu, Dong Liu, Minerva Garcia-Barrio, Minerva T. Garcia-Barrio, Robert N Taylor, Bert Gold, Samantha Jefferson, Neil Sidell, Winston E. Thompson, Winston Thompson
Cell and tissue research · 2016 · vol. 365(1) , pp. 187–196 · doi:10.1007/s00441-016-2358-1 · PMID:26841879 · W2259541200
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Exosomes isolated from endometriotic stromal cells exhibited enhanced angiogenic effects on endothelial cells and displayed differential microRNA profiles compared to controls.

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The paper investigates whether exosomes released by human primary endometrial stromal cells (ESCs) from women with endometriosis contain microRNA profiles associated with angiogenesis, and tests their functional effects on endothelial cells in vitro. ESCs were derived from five women with endometriosis (from eutopic endometrium and lesion tissue) and five phase-matched controls with normal endometrium, exosomes were isolated and characterized, and exosomal microRNAs were profiled by deep sequencing/RT-qPCR, with uptake assessed by confocal microscopy and angiogenic effects measured by treating HUVECs with ESC-derived exosomes. Exosomes from endometriosis lesion cells showed differential exosomal miRNA expression versus control ESC exosomes, and demonstrated both autocrine cellular uptake by ESCs and paracrine pro-angiogenic effects on HUVECs; the authors note limitations including the small sample size and lack of age-matching between groups. This paper is centrally about endometriosis — exosomes from endometriotic stromal cells are shown to enhance angiogenic effects in vitro, linked to differential exosomal microRNA cargo.

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Abstract

Our objective has been to establish a pro-angiogenic role for exosomes in endometriosis and to determine whether a differential expression profile of cellular and exosomal microRNAs (miRNAs) exists in endometriosis. We performed an in vitro study of human primary endometrial stromal cells (ESCs) and human umbilical vein endothelial cells (HUVECs). We isolated and characterized exosomes from ESCs from five endometriosis patients and five phase-matched controls. Exosomes were characterized by transmission electron microscopy and NanoSight technology. MiRNA was assessed by deep sequencing and reverse transcription with quantitative polymerase chain reaction. Exosome uptake studies were achieved by means of confocal microscopy. The pro-angiogenic experiments were executed by treating HUVECs with ESC-derived exosomes. We observed differential profiles of exosomal miRNA expression between exosomes derived from endometriosis lesion cells and diseased eutopic stromal cells compared with exosomes derived from control ESCs. We also demonstrated autocrine cellular uptake of exosomes and paracrine functional angiogenic effects of exosomes on HUVECs. The results of this study support the hypothesis that exosomes derived from ESCs play autocrine/paracrine roles in the development of endometriosis, potentially modulating angiogenesis. The broader clinical implications are that Sampson's theory of retrograde menstruation possibly encompasses the finding that exosomes work as intercellular communication modulators in endometriosis.
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Abstract

Our objective has been to establish a pro- angiogenic role for exosomes in endometriosis and to deter- mine whether a differential expression profile of cellular and exosomal microRNAs (miRNAs) exists in endometriosis. We performed an in vitro study of human primary endometrial stromal cells (ESCs) and human umbilical vein endothelial cells (HUVECs). We isolated and characterized exosomes from ESCs from five endometriosis patients and five phase- matched controls. Exosomes were characterized by transmis- sion electron microscopy and NanoSight technology. MiRNA This work was supported by NIH grants 5U01HD066439 and 1R01HD057235. This publication was also supported by the Research Centers in Minority Institutions Grant Number 8G12MD007602 from the National Institute of Minority Health and Health Disparities (NIMHD) and 8U54MD007588. The content of this publication is solely the responsibility of the authors and does not necessarily represent the official views of the NIMHD or the NIH. Electronic supplementary material The online version of this article (doi:10.1007/s00441-016-2358-1) contains supplementary material, which is available to authorized users. * Djana Harp [email protected] Adel Driss [email protected] Sharifeh Mehrabi [email protected] Indrajit Chowdhury [email protected] Wei Xu [email protected] Dong Liu [email protected] Minerva Garcia-Barrio [email protected] Robert N. Taylor [email protected] Bert Gold [email protected] Samantha Jefferson [email protected] Neil Sidell [email protected] Winston Thompson [email protected] 1 Department of Obstetrics and Gynecology, Morehouse School of Medicine, 720 Westview Drive, SW , Atlanta GA 30310, USA 2 Cardiovascular Research Institute, Morehouse School of Medicine, 720 Westview Drive, SW, Atlanta GA 30310, USA 3 Department of Physiology, Morehouse School of Medicine, 720 Westview Drive, SW, Atlanta GA 30310, USA Cell Tissue Res (2016) 365:187–196 DOI 10.1007/s00441-016-2358-1 was assessed by deep sequencing and reverse transcription with quantitative polymerase chain reaction. Exosome uptake studies were achieved by means of confocal microscopy. The pro-angiogenic experiments were executed by treating HUVECs with ESC-derived exosomes. We observed differ- ential profiles of exosomal miRNA expression between exosomes derived from endometriosis lesion cells and dis- eased eutopic stromal cells compared with exosomes derived from control ESCs. We also demonstrated autocrine cellular uptake of exosomes and paracrine functional angiogenic ef- fects of exosomes on HUVECs. The results of this study sup- port the hypothesis that exosomes derived from ESCs play autocrine/paracrine roles in the development of endometriosis, potentially modulating angiogenesis. The broader clinical im- plications are that Sampson ’s theory of retrograde menstrua- tion possibly encompasses the finding that exosomes work as intercellular communication modulators in endometriosis.

Keywords

Exosomes . Endometrial stromal cells . Angiogenesis . MicroRNA . Infertility

Introduction

Endometriosis is a benign gynecological disorder character- ized by the presence of endometrial glandular tissue and stro- ma outside of their normal uterine location. Up to 10 % of reproductive-age women in the United States are estimated to have endometriosis, which is associated with debilitating pain, menstrual irregularities, and infertility in as many 30 % of the affected women (Bulun 2009; V erkauf 1987). The precise etiology of endometriosis remains to be elucidated. Commonly accepted theories of the causes of endometriosis include retrograde menstruation, coelomic metaplasia, and lymphatic and vascular dissemination (Macer and Taylor 2012). Patients with endometriosis often have delayed (6 – 11 years) diagnosis because symptoms are variable and often mimic other gynecological diseases (Fassbender et al. 2015; Leone Roberti Maggiore et al. 2016; Nogales et al. 1993). A definitive diagnosis of endometriosis requires surgery (Gordts et al. 2015). The development of new ways of diagnosis by using exosomal biomarkers might enable earlier diagnosis of the disease (Fassbender et al. 2015). Angiogenesis, the formation of new blood vessels, has in- creasingly been recognized as a key pathological factor in endo- metriosis. Human endometrialtissue is known to be angiogenic throughout the menstrual cycle (Maas et al. 2001). Sampson’s theory of retrograde menstruationposits that endometrial tissue travels retrogradely through the Fallopian tubes and is deposited into the peritoneal cavity, where it establishes a blood supply, proliferates, and forms an implantthat is clinically recognized as al e s i o n( S a m p s o n1927). Women with endometriosis have been found to have increased retrograde menstruation (Halme et al. 1984). Successful implantation of endometriotic lesions depends on neovascularization, fibrosis, adhesion formation, apoptosis evasion, and neuronal infiltration (Rocha et al.2013). The exact mechanisms underlying the sprouting and sustainment of endo- metriosis neovascularization need further clarification. Recent studies, however, demonstrate that inhibitors of angiogenesis block the progression of endometriosis (Edwards et al. 2013; Nap et al. 2004,W a n ge ta l .2014). Exosomes have been found to play physiological roles as mediators of intercellular cell signaling between neighboring cells and even amongst distant tissues, and they may act inde- pendently but synergistically with soluble growth factors and hormones (Colombo et al.2014). Exosomes are vesicles rang- ing from 30 to 150 nm in diameter, are derived from the fusion of multivesicular bodies with the plasma membrane, and are secreted by a variety of living cells; they are composed of a lipid bilayer membrane and contain functionally active pro- teins, mRNA and microRNA (miRNA) that can be released, rendering them important mediators of intercellular commu- nication (Colombo et al. 2014). The recent discovery of these extracellular organelles containing genetic cargo with a unique signature raises the hope that exosomes will serve as diagnostic markers or therapeutic vehicles (Krause et al.2015; Momen-Heravi et al. 2015;T a n ga n dW o n g2015). Among all molecules, the miRNAs that are contained with- in exosomes (V aladi et al.2007) could affect gene expression and function in target cells, including vascular endothelial cel ls. Several miRNAs, such as miR-21 and miR-126, have been shown previously to play critical roles in angiogenesis (Wang and Olson 2009). We have chosen to screen these two miRNAs because, in previous literature, they have been wide- ly used by the scientific community as pro-angiogenic indica- tors in other systems (Bao et al. 2012; Guduric-Fuchs et al. 2012;X ue ta l . 2015). Additionally, endometrial exosomes released into the uter- ine cavity can transfer information either to the blastocyst or to other cells in the endometrium to influence implantation (Ng et al. 2013). Our hypothesis is that exosomes released from endometriotic stromal cells contribute to the pathogenesis of endometriosis by packaging and delivering specific miRNAs in an autocrine and paracrine fashion. In this study, we have examined exosomes as delivery vehicles for pro-angiogenic miRNA in endometriosis. 188 Cell Tissue Res (2016) 365:187–196 4 Department of Obstetrics and Gynecology, Wake Forest School of Medicine, 1 Medical Center Boulevard, Winston-Salem NC 27157, USA 5 Center for Cancer Research, National Cancer Institute, Frederick MD 21702, USA 6 Georgia State University, P .O. Box 3965, Atlanta GA 30302, USA 7 Department of Gynecology & Obstetrics, Emory University School of Medicine, 1639 Pierce Dr., WMB 4303, Atlanta GA 30322, USA

Materials and methods

Human subjects and tissue acquisition The study was approved by the institutional review boards of the Emory University School of Medicine and Morehouse School of Medicine. The primary endometrial stromal cells (ESCs) were obtained from normally cycling, reproductive- age women undergoing surgery for benign gynecological con- ditions with normal endometrium (NE, n = 5) and 5 women with endometriosis who provided eutopic endometrial biop- sies (EE, n = 5) plus specimens from their endometriosis im- plants (EI, n = 5). For NE controls, endometrial tissues were obtained from patients undergoing surgery for clinical indica- tions, typically infertility, pelvic pain, or suspicion of a pelvic mass, or some combination of findings under protocols ap- proved by the Institutional Review Boards of the Emory University School of Medicine and Morehouse School of Medicine. All the subjects selected were women who had regular menstrual cycles and who had not received hormonal therapy for at least 3 months before surgery (Y u et al. 2014). Absence of endometriosis in the NE group was confirmed after surgical examination of the abdominal and pelvic cavity. Specimens from controls were obtained from normally cy- cling women undergoing surgery for benign gynecological conditions in which no endometriosis or evidence of endome- trial abnormalities was visible. Among the five control sub- jects, subserosal fibroids were noted in four women, and none were greater than 3 cm in diameter. Endometriosis patients were identified at surgery by expert laparoscopists familiar with the varied appearance of the lesions. Although the sub- jects were not age-matched, their mean ages were not signif- icantly different (Control, 40.4 ± 5.9; Endometriosis, 34.0 ±7 . 8 ;P = 0.53). The secretory menstrual phase according to the day of the reproductive cycle was selected for all biopsies to maximize consistency and was confirmed by histological examination of the endometrial tissues. Written informed con- sent was obtained prior to surgical removal of endometriotic lesion tissue and endometrial biopsies. Cell cultures and reagents Primary ESCs were prepared from human tissue biopsies ac- cording to our published procedure (Ryan et al. 1994). All cultures (passages 3 –5) were grown in complete medium to 70–90 % confluence in DMEM/Ham ’s F-12 supplemented with 10 % fetal bovine serum (FBS), 1 % non-essential amino acids, 1 % sodium pyruvate, and 1 % penicillin streptomycin and were incubated at 37 °C and 5 % CO 2. Human umbilical vein endothelial cells (HUVECs) were purchased from Lonza (Walkersville, Md., USA) and were cultured in EBM-2 media supplemented with EGM-2 MV cocktail (Lonza) together with 1 % penicillin and streptomycin. Isolation of exosomes Once the desired confluence was obtained, the culture media were removed, and ESCs were washed twice with 5 ml sterile phosphate-buffered saline (PBS). The ESCs were then cul- tured for an additional 48 h with growth media containing exosome-depleted FBS. Exosome-depleted FBS was obtained by ultracentrifugation of FBS at 100,000 g for 16 h at 4 °C. The exosomal fraction from 5 ml culture media was isolated by the Total Exosome Isolation kit (Invitrogen) according to the manufacturer’s recommendations. First, the collected cell culture media were centrifuged at 2000 g for 30 min at room temperature to remove cells and debris. Second, a half-volume of the exosome isolation solution was added to cell-free cul- ture media, and samples were refrigerated at 4 °C overnight. The mixture was centrifuged at 10,000 g for 1 h at 4 °C, and the supernatant was removed by aspiration. The pellet was re- suspended in 1× PBS and stored at −80 °C or directly proc- essed for miRNA extraction (Li et al. 2015). Identification of nanoparticles by nanoparticle tracking analysis Nanoparticle tracking analysis (NTA) measurements were performed by using a NanoSight NS500 instrument (NanoSight NTA 2.3 Nanoparticle Tracking and Analysis Release V ersion Build 0025). The size distribution and quan- tification of exosome preparations were analyzed by measur- ing the rate of Brownian motion with a NanoSight LM10 system (NanoSight, Wiltshire, United Kingdom) equipped with fast video capture and p article-tracking software. Purified exosomes from NE, EE, and EI samples were diluted in 500 μl of a solution of 1× PBS/5 mM EDTA and disaggre- gated by using a syringe and needle (29-gauge). After this procedure, the sample was injected into a NanoSight sample cubicle. The mean ± SD size distribution of ESC exosomes was determined, and the mean number of particles per milli- liter was compared between endometriosis patients (exosomes derived from EE and EI ESCs) and exosomes derived from eutopic NE cells of healthy subjects (Riches et al. 2014). Exosome visualization by transmission electron microscopy Exosome suspension was loaded into a carbon-coated electron microscopy grid. The sample was fixed with 2.5 % glutaral- dehyde in 0.1 M cacodylate buffer for 2 h at 4 °C, followed by a second fixation with 1 % osmium tetroxide in 0.1 M cacodylate buffer for 1 h at 4 °C. After three washes in dis- tilled H 20, the sample was stained with 0.5 % aqueous uranyl acetate for 2 h at room temperature. Transmission electron microscopy samples were observed by using a JEOL 1200EX instrument. Cell Tissue Res (2016) 365:187–196 189 Exosome labeling Exosomes were first obtained from non-labeled ESCs as described above. The protein content of the exosomes was adjusted to 1.4 μg/ml prior to labeling. Exosomal membrane was labeled with BODIPY TR ceramide, ac- cording to the manufacturer ’s protocol (Molecular Probes/Invitrogen Life Technologies). Briefly, exosome pellets were re-suspended in 100 μl PBS and stained with 10 μmol/L BODIPY TR ceramide with 594- Alexa-Fluor (red) fluorescence. Excess fluorescent dye was removed by using Exosome Spin Columns (Life Technologies). Confocal microscopy and imaging Cells were cultivated on chamber slides, treated with a final concentration of 28 ng/ml labeled exosomes (red) for 20 min, fixed with 4 % paraformaldehyde at room temperature for 20 min, permeabilized with ice-cold ac- etone at room temperature for 5 min, and then stained with fluorescent 488-Phalloidin (green) for actin using the manufacturer ’s recommendations (Molecular Probes/ Invitrogen Life Technologies). Fluorescence images were collected on an inverted microscope (Zeiss LSM- 700) via a 40× objective. Zeiss acquisition parameters, including exposure, focus, illumination, and Z stack projection, were controlled by ZEN 2 software (Carl Zeiss Microscopy). For the analysis of the cellular in- ternalization of exosomes, images were also deconvolved by using ZEN 2 software (Chu et al. 2012). Endothelial tube formation assay Sub-confluent HUVECs were ha rvested, resuspended in medium, and treated with the indicated concentration of exosomes or with PBS as a negative control. The exosome protein concentration was measured by the Coomassie Plus (CP) Protein Assay (Thermo Sci entific). Treatment of cells consisted of 50 μg total excreted exosomes extracted from eutopic endometriosis and control endometrial cells. This suspension was seeded (70,000 cells/well) in growth- factor-reduced Geltrex Basement Membrane Matrix (Gibco) on a 96-well plate (BD Bioscience) and incubated up to 24 h at 37 °C with 5 % CO 2. Tube formation was examined under an inverted microscope and photographed at 40× magnification. Cumulative tube length was mea- sured by using ImageJ software (Schneider et al. 2012).

Results

are shown as the mean and standard errors of trip- licate experiments (Swift et al. 2010). Micro-RNA extraction, deep sequencing, and reverse transcription with quantitative polymerase chain reaction Micro-RNA was extracted from exosomes and cells by using the mir Va n a miRNA isolation kit (Life Technologies) according to the manufacturer ’sp r o t o c o l . RNA concentration and relative quality were determined by using a Nanodrop Spectrophotometer (Thermo Scientific). Samples were deemed acceptable if 260/280 ratios were greater than 1.6; 260/230 ratios were greater than 1.0. miRNA (1 μg) was reverse-transcribed by using the TaqMan MicroRNA Reverse Transcription Kit (Applied Biosystems) following the manufacturer ’sp r o t o - col. Primers for hsa-miR-21-5p (Cat. no. 4427975- 000397), hsa-miR-126-5p (Cat. no. 4427975-000451), and U6 snRNA (Cat. no. 4427975-001973) were used from miRNA kits (Applied Biosystems), and real-time quantitative polymerase chain reaction (qPCR) was per- formed by using the LC480 Lightcycler thermocycler (Roche). snRNA U6 was used as an endogenous control to normalize expression data. All samples were run in triplicate, and the average v alue was used to calculate the fold change values. The delta-delta of average Ct/Cp value method was used to calculate the fold change values among samples as previously described (Scarlett et al. 2014). Deep sequencing of total miRNAs was carried out by SeqMatic LLC (Fremont, Calif., USA). Illumina se- quencing libraries were generated by using the SeqMatic TailorMix miRNA sample preparation kit. Sequencing was performed by using the Illumina Genome Analyzer IIx with a 1 × 36 bp single-end read. Data was de- multiplexed by index barcode, and fastq files were gener- ated by using Illumina pipeline (CASA V A). For data qual- ity control, sequence reads were trimmed of the Illumina adapters by using fastx clipper. Reads shorter than 15 bp were removed from subsequent analyses. For data analy- sis, clean sequence reads were mapped to the human ge- n o m e( h g 1 9 )a n dt om i R B a s ev e r s i o n2 0b yu s i n gB o w t i e . Parameters were modified to allow for up to one mis- match. Reads mapping to known miRNAs were counted. Differential expression and P-value estimation were per- formed by using DESeq for R statistical programming language (Ge et al. 2014). Statistics Real-time qPCR results were expressed as means ± standard deviation (SD) from at least three separate experiments per- formed in triplicate, unless otherwise stated. Differences be- tween means among the treatment groups were analyzed by using the Student two-tailed t-test or one-way analysis of var- iance (ANOV A) with Holm-Sidak post-tests method where appropriate. Quantitative analysis of branching length in the 190 Cell Tissue Res (2016) 365:187–196 angiogenesis assay was performed with Pearson correlation analysis. A P-value of <0.05 was considered significant. SigmaPlot (version 11.0) and MS Excel software for Windows were used for statistical analysis.

Results

Identification of ESC-derived exosomes in culture media The ESC exosome purification procedure was validated by u s i n ge l e c t r o nm i c r o s c o p ya n dN a n o S i g h ta n a l y s i s . Figure 1a shows an example of a transmission electron micrograph of a representative exosome preparation. Further characterization of exosomes, including size measurement and quantification, from healthy (Fig. 1b–d, Supplementary video 1) and endometriosis subjects was performed by using NanoSight analysis, which demonstrated the purity of the vesicles, with a peak size at 35 nm. This confirmed that the ESCs of control and endometriosis subjects released exosomal vesicles into their conditioned medium. No measurable differences were observed in size or yield (Fig. 1e, f). Autocrine internalization of exosomes by ESCs We hypothesized that exosomes work in an autocrine/ paracrine fashion and can be internalized by nearby cells to affect function in the uterine microenvironment or peritoneal cavity. The internalization of labeled puri- fied exosomes was visualized by confocal fluorescence microscopy in ESCs (Fig. 2a–g, Supplementary Fig. S1, Supplementary video 2). We observed that the internal- ization of exosomes occurred within 2 min of exposure to treatment, suggesting a fast uptake mechanism (Fig. 2h, i). In these experiments (Fig. 2), we observed the uptake of exogenous purified NE exosomes by NE ESCs. Similar results were found when we used EE exosomes on NE cells, and when we used EE cells. The findings support the ability of exosomes to influ- ence cell behavior via autocrine and/or paracrine routes. Fig. 1 a Transmission electron microscopy of exosomes from control endometrial stromal cells (ESCs). Bar 100 nm. b Scatter plot graph of exosomes by using Nanosight technology shows that the majority of exosomes are between 20 and 200 nm in size with a peak at 35 nm (X = particle size, Z = count/ml). c Curve 1 describes the relationship between particle number distribution (concentration/ml; left Y axis)a n d particle size (in nm;Xa x i s); curve 2 describes the correlation between the cumulative percentage distribution of particles (percentile; right Y axis) and particle size ( Xa x i s). d Still figure of exosome scatter nanoparticle tracking in a NanoSight video (Supplementary video 1). e Repeated- measure analysis of variance showing scatter plot column comparison of means of exosome concentrations between the three groups ( NE normal endometrium, EE eutopic endometrium, EI endometriosis implants). No measurable differences between the three groups were observed ( P = 0.655). f Scatter plot column comparison of means of exosome sizes between the three groups. No measurable differences between the three groups were observed ( P =0 . 5 2 9 ) .Error bars are the standard deviations of the different readings from different isolations from T -75 flasks after 24 h of changing to exosome-free medium Cell Tissue Res (2016) 365:187–196 191 Pro-angiogenic effects of exosomes derived from ESCs HUVECs plated on Geltrex Basement Membrane Matrix in medium treated with exosomes extracted from eutopic endo- metriosis ESC medium had greater tube formation compared with those treated with exosomes extracted from control ESC medium (Fig. 3a, b). A significant increase (P =0 . 0 3 3 )o ft o t a l segment branch length was noted on HUVECs treated with exosomes extracted from endometriosis cells compared with control cells (Fig. 3c). Differential expression of exosomal pro-angiogenic miRNAs Deep sequencing data also showed that several miRNAs extracted from exosomes of NE and EE were differentially expressed between the two groups (Fig. 3d). The deep se- quencing results led to the identification of several miRNAs that have yet to be characterized and confirmed in a larger patient sample size. As angiogenesis has been recognized to be a key pathological factor in endometriosis, we found, from our deep sequencing heat-map data, that some miRNAs could be predicted to be involved in the angiogen- esis process. Since our endothelial tube assay showed pro- angiogenic effects in EE-treated HUVECs, we analyzed two known pro-angiogenic miRNAs (miR -21 and miR- 126) to determine whether differe ntial expression occurred. We investigated the expression in total miRNA extracted from exosomes secreted by NE, EE, and EI ESCs. Whereas the data did not reveal significant differences in miR-126 among samples, EI cells showed an 11-fold in- crease in miR-21 expression versus the healthy control eutopic ESC exosomes ( P < 0.0001; Fig. 3e, f ). Intracellular expression levels of miR-21 and miR-126 ex- tracted from the producing cells in culture showed no sig- nificant differences between groups (Fig. 3g, h). Fig. 2 Uptake of exosomes by NE ESCs. The protein equivalent of 28 ng/ml labeled exosomes ( red) was incubated for 20 min with ESCs, which were then fixed in 4 % paraformaldehyde at room temperature for 20 min, subsequently permeabilized with ice-cold acetone at room temperature for 5 min, and finally labeled with 488-Phalloidin ( green). Similar results were obtained when we used NE and EE exosomes, and when we used EE cells. a ESCs labeled with 488-Phalloidin ( green). b Exosomes labeled with 594-Alexa-Fluor ( red). c Merged image. a–c Magnification: 40×. d–f Higher magnification of boxed areas in a–c. g Z-stack slices running apical to basolateral in ESCs showing the ZX (upper box) and ZY ( right side box ) cross sections of the selected cells (Supplementary video 2) showing that the exosomes ( red) are located inside the ESCs and not on the top or bottom. h Uptake by the ESCs of exosomes after 2 min of treatment. i Uptake by the ESCs of exosomes after 8 min of treatment 192 Cell Tissue Res (2016) 365:187–196

Discussion

Angiogenesis is necessary for the establishment and prolifer- ation of endometriotic lesions (Shifren et al. 1996). Many molecules and various mechanisms involved in lesion angio- genesis are currently under study (Araldi et al. 2015;K a z a n i s et al. 2015;L ie ta l . 2015). We have demonstrated exosome release from ESCs and confirmed the presence of exosomes by morphological anal- ysis and dimensions. We have shown that the exosomes are rapidly uptaken by ESCs in vitro (Fig. 2). No morphological difference has been noted following the uptake of exosomes from NE cells and from EE cells by either cell type. We pos- tulate that specific surface ligands allow the highly efficient and targeted uptake of these vesicles by recipient cells, as has been shown in other cell types (Schneider and Simons 2013). We hypothesize that ESC-released exosomes are taken up by and have a pro-angiogenic effect on endothelial cells that helps to promote tube formation. We have further shown dif- ferential exosomal angiogenic activity on HUVECs in the in vitro Matrigel assay. Endothelial cells are integrally necessary for the formation of new blood vessels. We have observed increased branching when the HUVECs are treated with EE exosomes compared with NE exosomes (Fig. 3a–c). These data suggest that exosomes play a role in promoting endothe- lial cell formation and angiogenesis in endometriosis. Exosomes from a variety of other cell types have been shown to exert a pro-angiogenic effect on endothelial cells and on stromal cells (Mineo et al.2012;P a g g e t t ie ta l .2015;P a s c u c c i et al. 2014). From our data, we propose that exosomes can play an important mediator role in the angiogenesis process in vitro in a paracrine fashion. In the present study, we show that ESCs release biological- ly functional exosomes that can facilitate angiogenesis in a validated in vitro assay. Exosomes carry a variety of bioactive molecules: RNAs, DNAs, proteins, and lipids (Colombo et al. 2014). The various types of response in target cells induced by exosomes derived from parent cells are probably determined by their miRNA content (Pascucci et al. 2014; Shabbir et al. 2015). Our deep sequencing data suggest that endometriosis Fig. 3 a HUVECs treated with exosomes extracted from control cells at 24 h. b HUVECs treated with exosomes extracted from endometriosis patient cells at 24 h. c Significant increase of total segment branch length is noted on HUVECs treated with exosomes extracted from EE cells compared to those from NE cells ( error bar SD). d Heat-map from deep-sequencing depicting the most significant differential expression of miRNAs extracted from exosomes of NE and from EE. e, f miR-21 and miR-126 expression, respectively, revealed by reverse transcription and quantitative polymerase chain reaction (RT-qPCR) of RNA extracted from exosomes from NE, EE, and EI samples. EI cells showed an 11-fold increase in miR-21 expression versus the healthy control eutopic ESC exosomes (P < 0.0001). No significant difference in miR-126 expression was found among samples. g, h miR-21 and miR-126 expression, respectively, revealed by RT -qPCR of RNA extracted from cells of NE, EE, and EI samples. No significant differences between groups were shown between intracellular expression levels of miR-21 and miR-126 extracted from the producing cells in culture Cell Tissue Res (2016) 365:187–196 193 patients have a differential expression of exosomal miRNA patterns compared with controls (Fig. 3d). This signifies that differential pathogenic roles and altered mechanisms are in- volved in exosomal intercellular communication in the perito- neal and intrauterine milieu. Our results indicate that at least one of these factors, name- ly the pro-angiogenic miRNA, miR-21, is differentially expressed in lesion exosomes of endometriosis-derived sam- ples (EI) relative to normal (NE) exosomes. Transferred exosomal miRNA can reprogram the recipient cells. The link- age between exosomal miRNAs and their effects in the recip- ient cells remains to be fully elucidated. However, evidence to date indicates that exosomes are powerful mediators of intercellular communication (Tang and Wong2015). We pro- pose that the exposure of endothelial cells to ESC exosomes leads to angiogenesis, with some of the effects possibly being attributable to the overexpression of miR-21. Exosomes con- taining miR-21 have been previously reported to stimulate cell angiogenesis in other systems (Bao et al. 2012; Guduric- Fuchs et al. 2012 ;X ue ta l . 2015). We speculate that exosome-derivedmiRNAs are potential angiogenic targets that are relevant to endometriosis sequelae such as abnormal im- plantation and infertility. Thus, these exosome-specific miRNAs would be present in the uterine and peritoneal micro- environments mediating cross-talk essential for the constella- tion of secondary effects of endometriosis. The work Fig. 4 Suggested model depicting exosome shedding in the endometrial cavity working in an autocrine, paracrine, and endocrine manner. Exosomes may also be shed in a retrograde fashion with menstrual flow and be taken up by cells within the peritoneal cavity or shed by stromal cells in the menstrual flow 194 Cell Tissue Res (2016) 365:187–196 presented here sets the basis for a path toward the discovery of novel effective biomarkers for early diagnostics and potential new drug targets. This study supports the hypothesis that exosomes derived from endometriotic stromal ce lls play autocrine/paracrine roles in the endometrial and peritoneal microenvironments, modulating angiogenesis. Figure4 shows our suggested mod- el of action of exosomes in the uterine microenvironment. Additionally, exosomes can migrate further into other tissues through blood vessels (endocrine; De Toro et al. 2015;N g et al. 2013; Salomon et al. 2014; Simpson et al. 2008)a n d be transported to the peritoneal cavity through a retrograde flow deposition system. Furthermore, these lesion exosomes might modify angiogenesis in the local peritoneal environment. The broader clinical implications discussed are built on Sampson’s theory of retrograde menstruation, a theory that supports the idea that exosomes work as intercellular commu- nication modulators in endometriosis. We suggest a model in which exosomes secreted from diseased endometrial cells stimulate the pro-angiogenic propensity of nascent lesions in the peritoneum to adopt a new vasculature and cause inflam- matory changes that lead to pelvic pain and infertility. This pathogenic intercellular transfer of genetic material mediated by exosome carriers could pave the road to new diagnostic and therapeutic tools in the field of reproductive biology. Acknowledgments The authors thank Mr. Lawrence Brako and Dr. Woo Kuen Lo for assistance with the electron microscopy, and Dr. Gregory Adams for technical assistance with the confocal microscopy at the MSM Core Facility. Compliance with ethical standards Conflict of interest The authors declare that they have no conflict of interest. Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http:// creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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mesh:D004715endometriosis

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Endometriosis Exosomes Neovascularization, Pathologic Adult Autocrine Communication Culture Media Culture Media Endometriosis Exosomes Exosomes Female Humans Human Umbilical Vein Endothelial Cells Human Umbilical Vein Endothelial Cells MicroRNAs MicroRNAs Neovascularization, Pathologic Stromal Cells Stromal Cells

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