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Exosomes for gene therapy effectively inhibit the endothelial-mesenchymal transition in mouse aortic endothelial cells

BMC Musculoskeletal Disorders volume 22, Article number: 1000 (2021) Cite this article

Abstract

Background

Heterotopic ossification (HO) can limit joint activity, causes ankylosis and impairs the function and rehabilitation of patients. Endothelial to mesenchymal transition (EndMT) plays an important role in the pathogenesis of HO, and high expression of SMAD7(Mothers Against Decapentaplegic Homolog 7) in endothelial cells can effectively reverse the TGF-β1 mediated EndMT. This article studied an appropriately engineered exosome with high biocompatibility and good targeting property to administrate SMAD7 gene therapy to inhibit the EndMT.

Methods

Exosomes from mouse aortic endothelial cells were cultured and harvested. DSPE-PEG and antibody CD34 were combined to exosomes to synthesize the endothelial cell targeting exosome vector (Exosome-DSPE-PEG-AbCD34). The biocompatibility, stability, targeting and cell internalization of exosome vector were tested, then the Exosome-DSPE-PEG-AbCD34 was loaded with Smad7 plasmid and administrated to MAECs to examine its therapeutic effect on EndMT of MAEC mediated by TGF-β1.

Results

The Exosome-DSPE-PEG-AbCD34 has no impact on MAEC cell viability at high concentration, and exosome-DSPE-PEG-AbCD34 could be stably stored at 4°C and 37°C for at least 8 days. Exosome-DSPE-PEG-AbCD34 has better targeting property to MAEC cells and can enter into the cells more effectively. The Exosome-DSPE-PEG-AbCD34-Smad7 could significantly increase the level of SMAD7, decrease the expression of TGF-β1, and effectively reverse the EndMT of MAEC mediated by TGF- β1 in MAEC cells.

Conclusions

The synthesized Exosome-DSPE-PEG-AbCD34-Smad7 has good biological properties and can effectively reverse the EndMT of MAEC mediated by TGF-β1. Thus, Exosome-DSPE-PEG-AbCD34-Smad7 may has the potential for the prevention and treatment of HO.

Peer Review reports

Background

Heterotopic ossification (HO) is an abnormal process of bone formation that occurs in muscle or connective tissue [1]. HO can lead to pain, decrease in the range of motion of adjacent joints, peripheral nerve compression, and pressure ulcers. HO also has a high morbidity rate, ranging from 10% to 36%. These factors make it become one of complications affecting the functional rehabilitation of elbow and hip fracture patients. Therefore, identifying methods to prevent and reverse the pathological process of HO has great economic and social value [2]. Previous studies have shown that progenitor cells in local soft tissue affected by inflammation niches and signaling pathways gradually differentiate into chondrocyte phenotype and osteoblast phenotype and finally form mature bone tissue to produce ectopic bone [3]. However, the pathological mechanisms and related signaling pathways of HO are still unclear [4, 5], and its prevention and treatment methods are limited.

Recent studies have shown that the endothelial mesenchymal transition (EndMT) pathway is important in the pathogenesis of HO [6, 7]. Endothelial markers were reported to be expressed in chondrocytes and osteocytes in ectopic bone of an HO animal model, which were different from normal osteocytes and chondrocytes, indicating that endothelial cells are associated with the occurrence and development of HO [8, 9]. Lounev et al. also proved that the stimulation of inflammatory mediators and signals in local tissue induce vascular endothelial cells transform into chondrocytes and osteocytes through the EndMT pathway, and form ectopic ossification via intramembrane osteogenesis and chondrogenic osteogenesis [10]. Therefore, EndMT can be used as a target to develop prevention and treatment methods for HO. There are a plenty of studies have found that the transcription products of Smad7 gene can competitively bind to type II TGF-β receptor, thus inhibiting the TGF-β signaling pathway and playing a negative regulatory role [11]. Our previous finding also indicated that SMAD7 overexpression in vascular endothelial cells can effectively block the TGF-β mediated EndMT signaling pathway and thereby attenuate HO. However, SMAD7 overexpression in vascular endothelial cells requires gene vectors with high biocompatibility, good sustained-release performance, high plasmid loading and good targeting properties. Lentiviral vector is a widely used gene vector, but it is difficult to use in clinical treatment due to the limitations of its targeting properties and biosafety.

Exosomes , a sort of saccular vesicles with a diameter of 30-150 nm secreted by living cells, are important mediators of "material exchange" as well as information transmission between cells [12, 13]. As a natural endogenous substance transporter, exosomes have the advantages of low toxicity, no immunogenicity and good permeability and are thus superior carriers for effective molecule delivery [14, 15]. At present, exosomes have been successfully loaded with small molecule such as drugs, miRNAs, genes and proteins for the treatment of cancer, Alzheimer's disease and other diseases [16,17,18,19,20,21]. Endothelial cells are now one of the most popular cell sources of exosomes due to their high purity and productivity, ease of availability, and lack of ethical issues. Exosomes produced by the endothelial cells share the similar marker molecules with progenitor cells and contribute to the physiological functions of endothelium as well as the pathogenesis of cardiovascular disease. Thus we selected exosomes derived from mouse aortic endothelial cells as the vehicles of gene therapy [12, 22].

In this study, we bound the DSPE-PEG-AbCD34 (antibody of CD34) to the surface of secretory exosomes to synthesize exosome gene vector (Exosome-DSPE-PEG-AbCD34) with high endothelial cell targeting property. Then we loaded the Smad7 plasmid into the Exo-DSPE-PEG-AbCD34 and examined its effect on the TGF-β mediated EndMT pathway. Our study thus provides a new approach for the clinical prevention and treatment of HO.

Materials and Methods

Cell culture

Mouse aortic endothelial cells (MAEC) were purchased from ATCC. The cells were cultured in DMEM medium containing 10% FBS and 5% CO2 at 37°C. When the cell density reached 85%, the cells were digested with trypsin solution and passaged.

Exosome isolation

The exosomes of MAEC were extracted using the Invitrogen™ Total Exosome Isolation kit according to the manufacturer’s instructions. Briefly, 1ml of cell-free culture media was mixed with 500 μl Exosome Isolation reagent and incubated at 4°C for overnight. The mixed solution was centrifuged at 10,000 × g for 1 hour, supernatant was discarded and exosome pellets were resuspended for the following experiments.

Preparation of Exo-DSPE-PEG-AbCD34

As exosome membrane, mainly composed of lipid membrane, is rich in cholesterol, sphingomyelin and ganglioside, liposoluble compounds are therefore easy to be integrated into exosome membrane [23]. DSPE-PEG-AbCD34 was synthesized by conjugating CD34 antibody to DSPE-PEG2000-NHS. Then the exosomes were treated with DSPE-PEG-AbCD34. The lipophilic DSPE was fused into the exosome membrane, meanwhile the PEG-AbCD34 was carried to the exosome surface. The procedures were as follows: firstly, DSPE-PEG-AbCD34 was synthesized by the reaction of DSPE-PEG2000-NHS with excessive AbCD34 at room temperature for 24 hours. Then the prepared exosomes were dispersed in PBS, and the exosome protein content was adjusted to 50 mg/ml. 0.1 mL DSPE-PEG-AbCD34 solution with a concentration of 20 mg/mL was added to 2 ml of exosome dispersion, then the mixture was gently blown and incubated at room temperature for 1 hour. After that, the dispersion solution was transferred into a special centrifuge tube and ultracentrifuged at 120,000g and 4 °C for 70 min. The upper solution was sucked away and the unbound DSPE-PEG-AbCD34 was removed. The precipitate obtained was Exo-DSPE-PEG-AbCD34 connected with AbCD34. The precooled PBS solution was added to the precipitate to blow and dissolve again for standby.

Transmission electron microscope (TEM) detection

The purity and structural integrity of exosomes were determined by transmission electron microscopy (TEM), With the following procedure: The protein content of exosome dispersion was diluted to 100 mg/ml with HEPES buffer, then 10 uL exosome dispersion was added to 200 mesh copper mesh (covered with carbon film) for transmission electron microscopy, and the copper mesh was placed in a desiccator at room temperature until completely dried. Then samples were observed under the accelerated voltage of 75 kV, and photos were taken at the same time.

Detection of exosome particle size

First, the protein content of exosome dispersion was adjusted to 50 mg/mL, and 20 uL of exosome dispersion was added to 980 uL high ddH2O, then the particle size of exosome was measured by a potential particle size analyzer, based on a light scattering method.

CCK-8 assay

The concentration of logarithmic phase cells was adjusted to 5×104 cells/ml. 100 uL cell suspension was added into each well of a 96 well culture plate, and incubated in 5% CO2 incubator at 37°C for 24 h. After drug treatment, the supernatant was discarded, and 100 uL of fresh medium was added to each well, followed by 10 uL of CCK-8 solution. After 4 hours of culture at 37°C, the absorbance (OD) value of each well at 450 nm was detected by an enzyme reader.

The cell viability rate was calculated by the formula: Cell viability % = (OD sample - OD blank) / (OD control - OD blank) × 100.

Laser confocal microscopy detection

The cells were seeded in 96 well plates at the initial density of 1 × l05 cells per well. The cells were incubated with Exosome-DSPE-PEG-AbCD34 at 37°C for 2 h, then cultured in 60 nm lysotracker red medium at 37°C for 30 min, washed three times with cold PBS, and fixed with 4% paraformaldehyde for 20 min. Then, cells were treated with DAPI for 10 min and washed twice with PBS. The cells were observed by confocal laser scanning microscope (Olympus FluoView fv-1000, Olympus optics Co., Ltd., Tokyo, Japan) and observed with imaging software. The number of FITC positive cells in 10 visual fields in each group was counted, and the mean fluorescence of FITC intensity was calculated by use of imageJ 2.0.

qPCR assay

The total RNA was extracted using the Trizol (Invitrogen) kit according to the manufacturer’s instructions, then the mRNA was reversely transcribed into cDNA according to the manufacturer’s instructions of the TaqMan microRNA reverse transcription kit. The expression of each gene was detected using Applied Biosystems 7500 fluorescence quantitative PCR. The primers used were provided by SANGON Biotech (Shanghai) Co., Ltd. The primers designed in this paper are shown in Table 1.

Table 1 The qPCR primers used in manuscript
Full size table

SDS-PAGE gel electrophoresis and Western Blot

SDS-PAGE gel electrophoresis was used to detect AbCD34 on Exosome-DSPE-PEG-AbCD34, then an appropriate amount of RIPA cell lysate was added to the precipitate of exosome after 12,000g centrifugation and then incubated in an ice bath for 25 min. It was then centrifuged at 10,000g for 20 min. The BCA protein quantitative kit was used to quantify the protein concentration of exosomes and cell lysates. The lysate containing the same amount of protein was mixed with the SDS-PAGE sample loading buffer, heated to 100°C and kept for 5 min. The protein in the above mixture was separated by SDS-PAGE electrophoresis, then stained with R250 gel dyeing solution, and then decolorized with the decolorizing solution. The exosome marker proteins (CD9, CD63) [24], SMAD7, CD31, VE-cadherin, N-cadherin, vimentin and GAPDH were detected by western blot assay. Exosomes and cells were lysed by RIPA lysate, and after 12,000g centrifugation, the protein of exosomes and cell lysate was quantified using the BCA protein quantitative kit. The lysate containing the same amount of protein was mixed with the loading buffer to prepare samples. The protein samples were separated by SDS-PAGE and analyzed by western blot, then the protein was transferred to PVDF membrane by blot, and then sealed with 5% skim milk for 1 hour at room temperature. The first antibody corresponding to the detected protein was added and incubated at 4°C for 4 hours. After reacting with HRP labeled secondary antibody and washing, ECL luminous solution was used for exposure and photo recording.

Data analysis and statistical methods

Statistical data were expressed as mean ± SD, and one-way analysis of variance (ANOVA) was used for statistical analysis. *P < 0.05, * * P < 0.01 and * * P < 0.001 were regarded as significant differences. SPSS 18.0 software was used for statistical analysis.

Results

Preparation and characterization of Exosome-DSPE-PEG-AbCD34

Exosomes can be used as natural endogenous material carriers, and exosomes loaded with drugs have the advantages of low toxicity, no immunogenicity and good permeability. In this study, we first isolated exosomes from the MAEC culture medium of mouse aortic endothelial cells, and then synthesized Exosome-DSPE-PEG-AbCD34 by inserting the synthesized DSPE-PEG-AbCD34 into the exosome membrane structure. The exosomes were characterized by TEM (Fig. 1A) and potential particle size analyzer (Fig. 1B), the average diameter of prepared exosomes was about 150 nm. Western blot assay was used to detect exosome marker proteins (CD9, CD36) (Fig. 1C), as showed in the result, with CD9 and CD36 can be tested in exosome, meaning that the exosome was successfully extracted. CD34 antibody, which loaded on the outer membrane of the exosome, was detected by western blot assay, too (Fig. 1D, E). And the heavy chain and light chain of antibody was only showed in the exosome-DSPE-PEG-AbCD34. These results showed that we had successfully isolated and extracted MAEC exosomes from mouse aortic endothelial cells, and synthesized Exosome-DSPE-PEG-AbCD34 with CD34 targeting property.

Fig. 1
figure 1

Preparation of and characterization of Exosome-DSPE-PEG-AbCD34. A The TEM image of exosome isolated from MAEC cells (B) The size of exosome tested by potential particle size analyzer (C) Western blot assay was used to detect exosome marker proteins (CD9, CD63) (D) Western blot assay was used to detect CD34 antibody loaded on the outer membrane of the exosome and CD9 in the exosomes, (E) Western blot assay was used to detect CD34 antibody loaded on the outer membrane of the exosome and CD63 in the exosomes.

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Biocompatibility, stability, targeting property and cell internalization of Exosome-DSPE-PEG-AbCD34

Biocompatibility, stability, targeting and cell internalization are important characteristics of gene carriers. We used the CCK-8 assay to detect the effect of different concentrations of Exosome-DSPE-PEG-AbCD34 on the viability of MAEC cells. The results showed that treatment with the concentration from 10 to 320 ug/ml of Exosome-DSPE-PEG-AbCD34 had a negligible effect on cell proliferation and viability of MAEC cells (Fig. 2A). Then we tested the stability of Exosome-DSPE-PEG-AbCD34 at 4°C and 37°C by DLS and western blot assay (Fig. 2B, C). Results showed that after being stored at 4°C and 37°C for 8 days, the particle size of exosome-DSPE-PEG-AbCD34 could stably maintained at around 140 nm, which means the Exosome-DSPE-PEG-AbCD34 can be stably stored at 4°C and 37°C for at least 8 days. Then we observed the targeting effect of exosome-DSPE-PEG-AbCD34 on MAEC cells by laser confocal microscopy. The results showed that more FITC labeled exosome-DSPE-PEG-AbCD34 could be observed on the surface and inside of MAEC cells after the exosome vector and cells were incubated for 48 hours, which indicates that exosome-DSPE-PEG-AbCD34 has better cell targeting performance and cell internalization than exosome-DSPE-PEG (Figure 2D).

Fig. 2
figure 2

Biocompatibility, stability, targeting property and cell internalization of Exosome-DSPE-PEG-AbCD34. A Biocompatibility of Exosome-DSPE-PEG-AbCD34 to MAEC cells was tested by CCK-8 assay; B Stability of Exosome-DSPE-PEG-AbCD34 at 4 °C and 37 °C in different time; C western blot assay was used to detected the level of CD9 and CD36 at 4°C and 37°C in different time; D Confocal microscopy images of cell internalization testing of Exosome-DSPE-PEG-AbCD34 at ×20 magnification. The bar plot below shows the number of FITC positive cells and the calculated mean fluorescence of FITC intensity of each group. Scale bars: 2 μm.

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Synthesis of Exosome-DSPE-PEG-AbCD34-Smad7 and its effect on SMAD7 expression in MAEC cells

We incubated the Smad7 plasmid with Exosome-DSPE-PEG-AbCD34 to synthesize Exosome-DSPE-PEG-AbCD34- Smad7, and then DNA gel electrophoresis was used to detect the loading of pcDNA3.1- Smad7 in the Exosome-DSPE-PEG-AbCD34- Smad7 (Figure 3A). The result showed that pcDNA3.1- Smad7 can be loaded in the exosome, Exosome-DSPE-PEG and Exosome-DSPE-PEG-AbCD34. After exosome-DSPE-PEG-AbCD34- Smad7 was co-cultured with MAEC cells for 48 h, the gene level of SMAD7 in MAEC cells was detected by qPCR and western blot. The results showed that Exosome-DSPE-PEG-AbCD34 could transport pcDNA3.1- Smad7 into MAEC cells and overexpress SMAD7 successfully (Figure 3B, C and D).

Fig. 3
figure 3

Synthesis of Exosome-DSPE-PEG-AbCD34-Smad7 and its effect on SMAD7 expression in MAEC cells. A DNA gel electrophoresis was used to detect the loading of pcDNA3.1-Smad7 in the exosome, Exosome-DSPE-PEG and Exosome-DSPE-PEG-AbCD34; B qPCR assay was used to test the gene expression level of Smad7 after exosome, Exosome-DSPE-PEG and Exosome-DSPE-PEG-AbCD34 was co-cultured with MAEC cells for 48 h (C, D) Western blot assay was used to test the protein expression of SMAD7 after exosome, Exosome-DSPE-PEG and Exosome-DSPE-PEG-AbCD34 was co-cultured with MAEC cells for 48 h.

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The effect of Exosome-DSPE-PEG-AbCD34-Smad7 on EndMT pathway in MAEC cells

The EndMT has been proved to be an important mechanism in the pathogenesis of HO. In its molecular pathophysiological mechanism, the TGF-β (transforming growth factor-β) superfamily signaling pathway plays a leading role, and Smad7 is an important suppressor gene in this signaling pathway. To determine the inhibiting effect of Exosome-DSPE-PEG-AbCD34-SMAD7 on the EndMT of MAECS, we stimulated MAECS with 10 ng/ml TGF-β1 for 48 h to simulate the effect of TGF-β1 on local EndMT at the cellular level with or without the administration of Exosome-DSPE-PEG-AbCD34- Smad7. The effect of Exosome-DSPE-PEG-AbCD34-Smad7 on MAECS was detected by qPCR and western blot. The results showed that TGF-β1 could downregulate CD31 and VE-cadherin, and up regulate N-cadherin and vimentin. Compared with the control group, the Exosome-DSPE-PEG-AbCD34-Smad7 transfection group could apparently decrease the level of TGF-β1 in MAECs. Furthermore, the Exosome-DSPE-PEG-AbCD34-Smad7 can upregulate the expression of CD31 and VE-cadherin. Meanwhile, it also downregulated the expression of N-cadherin and vimentin (Figure 4C and D), which means it can then counteract the effect of TGF-β1 induced EndMT in MAECs. In conclusion, the overexpression of the SMAD7 induced by Exosome-DSPE-PEG-AbCD34-Smad7 can effectively reverse the EndMT pathway of MAECS mediated by TGF- β1.

Fig. 4
figure 4

The effect of Exosome-DSPE-PEG-AbCD34-Smad7 on EndMT pathway in MAEC cells. A qPCR assay was used to test the effect of Exosome-DSPE-PEG-AbCD34-Smad7 on the expression of TGF-β1 (B) Western blot assay was used to test the effect of Exosome-DSPE-PEG-AbCD34-Smad7 on the expression of TGF-β1, qPCR and western blot assay was used to test the mRNA expression (C) and protein expression (D) of EndMT pathway related genes (CD31, VE-cadherin, N-cadherin and vimentin).

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Discussion

Heterotopic ossification (HO) refers to the formation of atypical bone in muscle or at other sites of connective tissue, and HO which occurs around joints will develop clinical symptoms [25,26,27]. As a pathological bone formation, HO has an incidence rate vary from 9%-90%, and it can be influenced by several risk factors [4]. Severe HO can limit joint activity, even causing ankylosis and loss of joint function. It can also cause neurological symptoms and local pressure ulcers due to nerve wrapping [28]. Dyspareunia caused by heterotopic ossification of the adductor longus is also a rare complication [29]. Dynamic histomorphometry showed that compared with normal bone, ectopic ossified bone had higher metabolic activity, increased bone deposition rate, wider bone suture, and larger number of osteoblasts [30]. The fate of progenitor cells such as mesenchymal stem cells can be affected by stimulation from microenvironment [31, 32], and it has been proved that progenitor cells, inflammation niches and disorder of signaling pathway promote the formation of HO. Based on previous studies of HO related molecular mechanism and signaling pathway, we studied the targeted gene therapy method that may be used for the treatment of HO.

There were a plenty of studies indicating that the endothelial to mesenchymal transition (EndMT) plays an important role in the pathogenesis of HO. Under the regulation of inflammatory factors and the local neuroendocrine system, vascular endothelial cells pass through the vascular barrier, dissociate into tissues, and dedifferentiate into mesenchymal stem cells, then differentiate into chondrocytes and osteocytes under local conditions, and form HO tissue through the process of intramembrane osteogenesis and chondrogenic osteogenesis. EndMT was mainly induced by the TGF-β superfamily signaling pathway, and SMAD7 is an important suppressor gene of the TGF-β signaling pathway. Previous studies have shown that SMAD7 has the potential to prevent myofibroblast transformation and other EndMT progression, which verifies that high expression of SMAD7 in endothelial cells can effectively reverse the TGF-β1 mediated EndMT pathway of RAOECS. This result indicates that SMAD7 can be used in the prevention and treatment of HO [7]. The Smad7 gene needs the help of a gene vector with high biocompatibility and good targeting property to enter into the cells. Exosomes are small vesicles with a diameter of 30-150 nm naturally secreted by cells [33], and they can be used as potential carriers to deliver drugs, therapeutic genes or proteins in clinical treatment due to their stability and high biocompatibility [34,35,36,37]. In current study, the exosomes produced from mouse aortic endothelial cells were selected as vehicles of gene therapy as it mirror the marker molecules of parent cells and was associated with many physiological progresses such as anti-inflammation, anti-oxidation and the inhibition of endothelial-to-mesenchymal transition (EndMT) [12, 22]. However, normal exosomes cannot target specific cells. Loading targeted peptides with amphiphilic groups on the surface of exosomes can improve the targeting of exosomes.

The hydrophilic peptides always need to be modified by liposoluble compounds to integrate into the hydrophobic membrane of exosomes, which are mainly composed of lipid membrane. In this study, we used DSPE-PEG2000-NHS to bind CD34 antibody (AbCD34) to the surface of secreted exosomes to synthesize an exosome vector with a high endothelial cell targeting property (Exosome-DSPE-PEG-AbCD34). The assays we performed to detect its physical and biological characteristics showed that Exosome-DSPE-PEG-AbCD34 had no effect on MAEC cell viability at a high concentration, and Exosome-DSPE-PEG-AbCD34 could be stably stored at 4°C as well as room temperature for at least 8 days. Moreover, compared with Exosome-DSPE-PEG, Exosome-DSPE-PEG-AbCD34 has a better targeting property to MAEC cells and can enter into endothelial cells more effectively, which confirmed that the modification with antibody CD34 can remarkably develop exosomes’ ability to internalize into endothelial cells. Then we loaded Smad7 plasmid into the Exosome-DSPE-PEG-AbCD34 to compose the Exosome-DSPE-PEG-AbCD34- Smad7, and the transfection assay showed that Exosome-DSPE-PEG-AbCD34-Smad7 could significantly increase the level of SMAD7 in MAEC cells.

Finally, we examined the effect of Exosome-DSPE-PEG-AbCD34-Smad7 on the molecules related to the EndMT pathway in MAEC cells. The results showed that the Exosome-DSPE-PEG-AbCD34-Smad7 transfection group can up regulate the expression of CD31 and VE-cadherin, which proved that the Exosome-DSPE-PEG-AbCD34-Smad7 can counteract the effect of TGF-β1. Meanwhile, Exosome-DSPE-PEG-AbCD34-Smad7 transfection also downregulated the expression of N-cadherin and vimentin.

Conclusions

In conclusion, the overexpression of SMAD7 induced by Exosome-DSPE-PEG-AbCD34-Smad7 can effectively reverse the EndMT pathway of MAEC mediated by TGF- β1. These results indicate that Exosome-DSPE-PEG-AbCD34-Smad7 may has the potential for the prevention and treatment of HO. This study provides a theoretical basis and gene therapy strategy for the prevention and treatment of HO. Whether this modified method may be suitable for other sort of exosome and the concrete effect of Exosome-DSPE-PEG-AbCD34-Smad7 on prevention of HO progression should be studied in further research.

Availability of data and materials

The datasets generated and/or analyzed during the current study are available from the corresponding author by reasonable request.

Abbreviations

HO:

Heterotopic ossification

EndMT:

Endothelial to mesenchymal transition

SMAD7:

Mothers Against Decapentaplegic Homolog 7

MAECs:

Mouse aortic endothelial cells

TEM:

Transmission electron microscopy

References

  1. Zhang C, Zhong B, Luo C. Treatment strategy of terrible triad of the elbow: experience in Shanghai 6th People's Hospital. Injury. 2014;45(6):942–8.

    Article  Google Scholar 

  2. Brown K, Dharm-Datta S, Potter B, Etherington J, Mistlin A, Hsu J, et al. Comparison of development of heterotopic ossification in injured US and UK Armed Services personnel with combat-related amputations: preliminary findings and hypotheses regarding causality. J Trauma. 2010;69 Suppl 1:S116–22.

  3. Meyers C, Lisiecki J, Miller S, Levin A, Fayad L, Ding C, et al. Heterotopic Ossification: A Comprehensive Review. JBMR Plus. 2019;3(4):e10172.

    Article  Google Scholar 

  4. van Kuijk A, Geurts A, van Kuppevelt H. Neurogenic heterotopic ossification in spinal cord injury. Spinal Cord. 2002;40(7):313–26.

    Article  Google Scholar 

  5. Lin F, Wang N, Zhang T. The role of endothelial-mesenchymal transition in development and pathological process. IUBMB Life. 2012;64(9):717–23.

    Article  CAS  Google Scholar 

  6. Medici D, Olsen B. The role of endothelial-mesenchymal transition in heterotopic ossification. J Bone Miner Res. 2012;27(8):1619–22.

    Article  Google Scholar 

  7. Zhang C, Zhang Y, Zhong B, Luo C. SMAD7 prevents heterotopic ossification in a rat Achilles tendon injury model via regulation of endothelial-mesenchymal transition. FEBS J. 2016;283(7):1275–85.

    Article  CAS  Google Scholar 

  8. Medici D, Shore E, Lounev V, Kaplan F, Kalluri R, Olsen B. Conversion of vascular endothelial cells into multipotent stem-like cells. Nat Med. 2010;16(12):1400–6.

    Article  CAS  Google Scholar 

  9. Shui Y, Lv G, Shan L, Fan C, Tian N, Zhang L, et al. Epimedin C Promotes Vascularization during BMP2-Induced Osteogenesis and Tumor-Associated Angiogenesis. Am J Chin Med. 2017;45(5):1093–111.

    Article  CAS  Google Scholar 

  10. Lounev V, Ramachandran R, Wosczyna M, Yamamoto M, Maidment A, Shore E, et al. Identification of progenitor cells that contribute to heterotopic skeletogenesis. J Bone Joint Surg Am. 2009;91(3):652–63.

    Article  Google Scholar 

  11. Hua C, Wang Z, Zhang J, Peng X, Hou X, Yang Y, et al. SMAD7, an antagonist of TGF-beta signaling, is a candidate of prenatal skeletal muscle development and weaning weight in pigs. Mol Biol Rep. 2016;43(4):241–51.

    Article  CAS  Google Scholar 

  12. Zeng CY, Xu J, Liu X, Lu YQ. Cardioprotective Roles of Endothelial Progenitor Cell-Derived Exosomes. Front Cardiovasc Med. 2021;8:717536.

    Article  Google Scholar 

  13. Salimi L, Akbari A, Jabbari N, Mojarad B, Vahhabi A, Szafert S, et al. Synergies in exosomes and autophagy pathways for cellular homeostasis and metastasis of tumor cells. Cell Biosci. 2020;10:64.

    Article  CAS  Google Scholar 

  14. Nikfarjam S, Rezaie J, Kashanchi F, Jafari R. Dexosomes as a cell-free vaccine for cancer immunotherapy. J Exp Clin Cancer Res. 2020;39(1):258.

    Article  CAS  Google Scholar 

  15. Nikfarjam S, Rezaie J, Zolbanin NM, Jafari R. Mesenchymal stem cell derived-exosomes: a modern approach in translational medicine. J Transl Med. 2020;18(1):449.

    Article  Google Scholar 

  16. Elewaily M, Elsergany A. Emerging role of exosomes and exosomal microRNA in cancer: pathophysiology and clinical potential. J Cancer Res Clin Oncol. 2021;147(3):637–48.

    Article  CAS  Google Scholar 

  17. Yuan F, Zhou Z. Exosomes derived from Taxol-resistant nasopharyngeal carcinoma (NPC) cells transferred DDX53 to NPC cells and promoted cancer resistance to Taxol. Eur Rev Med Pharmacol Sci. 2021;25(1):127–38.

    CAS  PubMed  Google Scholar 

  18. Jena B, Mandal M. The emerging roles of exosomes in anti-cancer drug resistance and tumor progression: An insight towards tumor-microenvironment interaction. Biochim Biophys Acta Rev Cancer. 2021;1875(1):188488.

    Article  CAS  Google Scholar 

  19. Malm T, Loppi S, Kanninen K. Exosomes in Alzheimer's disease. Neurochem Int. 2016;97:193–9.

    Article  CAS  Google Scholar 

  20. Liu R, Liu J, Ji X, Liu Y. Synthetic nucleic acids delivered by exosomes: a potential therapeutic for generelated metabolic brain diseases. Metab Brain Dis. 2013;28(4):551–62.

    Article  CAS  Google Scholar 

  21. Alvarez-Erviti L, Seow Y, Yin H, Betts C, Lakhal S, Wood M. Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes. Nat Biotechnol. 2011;29(4):341–5.

    Article  CAS  Google Scholar 

  22. Mathiesen A, Hamilton T, Carter N, Brown M, McPheat W, Dobrian A. Endothelial extracellular vesicles: from keepers of health to messengers of disease. Int J Mol Sci. 2021;22(9):4640.

    Article  CAS  Google Scholar 

  23. Zhan R, Leng X, Liu X, Wang X, Gong J, Yan L, et al. Heat shock protein 70 is secreted from endothelial cells by a non-classical pathway involving exosomes. Biochem Biophys Res Commun. 2009;387(2):229–33.

    Article  CAS  Google Scholar 

  24. Kumar D, Gupta D, Shankar S, Srivastava R. Biomolecular characterization of exosomes released from cancer stem cells: Possible implications for biomarker and treatment of cancer. Oncotarget. 2015;6(5):3280–91.

    Article  Google Scholar 

  25. Eggli S, Woo A. Risk factors for heterotopic ossification in total hip arthroplasty. Arch Orthop Trauma Surg. 2001;121(9):531–5.

    Article  CAS  Google Scholar 

  26. Sirin E, Okay E, Khalilov T, Turkoz K, Erol B, Tetik C. Heterotopic ossification on the volar surface of the distal radius in a child with fibrodysplasia ossificans progressiva: challenges in surgical excision of a rare condition. Hand Surg Rehabil. 2021;40(2):194–7.

    Article  CAS  Google Scholar 

  27. Endo T, Imagama S, Kato S, Kaito T, Sakai H, Ikegawa S, et al. Association between vitamin A intake and disease severity in early-onset heterotopic ossification of the posterior longitudinal ligament of the spine. Glob Spine J. 2021;2192568221989300.

  28. Brooke M, Heard D, de Lateur B, Moeller D, Alquist A. Heterotopic ossification and peripheral nerve entrapment: early diagnosis and excision. Arch Phys Med Rehabil. 1991;72(6):425–9.

    CAS  PubMed  Google Scholar 

  29. Russell G, Perry M, Pearsall A. Heterotopic ossification of the adductor longus muscle presenting as dyspareunia. Am J Orthop (Belle Mead, NJ). 2000;29(11):879–82.

    Google Scholar 

  30. Wilkinson J, Stockley I, Hamer A, Barrington N, Eastell R. Biochemical markers of bone turnover and development of heterotopic ossification after total hip arthroplasty. J Orthop Res. 2003;21(3):529–34.

    Article  CAS  Google Scholar 

  31. Rezaie J, Mehranjani MS, Rahbarghazi R, Shariatzadeh MA. Angiogenic and Restorative Abilities of Human Mesenchymal Stem Cells Were Reduced Following Treatment With Serum From Diabetes Mellitus Type 2 Patients. J Cell Biochem. 2018;119(1):524–35.

    Article  CAS  Google Scholar 

  32. Heidarzadeh M, Keyhanmanesh R, Rezabakhsh A, Rahbarghazi R, Rezaie J, Saberianpour S, et al. Chronic asthmatic condition modulated the onset of aging in bone marrow mesenchymal stem cells. Cell Biochem Funct. 2021;39(6):821–7.

    Article  CAS  Google Scholar 

  33. Sheller-Miller S, Choi K, Choi C, Menon R. Cyclic-recombinase-reporter mouse model to determine exosome communication and function during pregnancy. Am J Obstet Gynecol. 2019;221(5):502.e501–12.

    Article  Google Scholar 

  34. Wang X, Tai Z, Tian J, Zhang W, Yao C, Zhang L, et al. Reducible chimeric polypeptide consisting of octa-D-arginine and tetra-L-histidine peptides as an efficient gene delivery vector. Int J Nanomedicine. 2015;10:4669–90.

    CAS  PubMed  PubMed Central  Google Scholar 

  35. Wang Y, Zhang Q, Yang G, Wei Y, Li M, Du E, et al. RPE-derived exosomes rescue the photoreceptors during retina degeneration: an intraocular approach to deliver exosomes into the subretinal space. Drug Deliv. 2021;28(1):218–28.

    Article  CAS  Google Scholar 

  36. Sahoo S, Kariya T, Ishikawa K. Targeted delivery of therapeutic agents to the heart. Nat Rev Cardiol. 2021;18(6):389–99.

    Article  Google Scholar 

  37. Rezaei R, Baghaei K, Amani D, Piccin A, Hashemi S, Asadzadeh Aghdaei H, et al. Exosome-mediated delivery of functionally active miRNA-375-3p mimic regulate epithelial mesenchymal transition (EMT) of colon cancer cells. Life Sci. 2021;269:119035.

    Article  CAS  Google Scholar 

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Acknowledgements

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Conflicts of interest

The authors declared no potential conflicts of interest with respect to the research, authorship, and publication of this article.

Funding

This work was supported by the National Natural Science Foundation of China [grant number 81772426], this funding was used to pay for costs associated with cell and reagents purchase; The Program of Science and Technology Commission of Shanghai [grant number 15dz2353800], this funding was used to pay for costs covering the use of instruments such as laser confocal microscopy; and the Shanghai Jiao Tong University Affiliated Sixth People’s Hospital’s own funds [grant number LYZY-0262], this funding was used to pay the fee of experiment technicians. All of funding bodies will not assist with study design, data interpretation and manuscript writing.

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Author notes

  1. Zhenyuan Wei and Yang Zhao contributed equally to this work and should be considered as co-first authors.

Authors and Affiliations

  1. Department of Orthopedic Surgery, and Shanghai Institute of Microsurgery on Extremities, Shanghai Jiao Tong University Affiliated Sixth People’s Hospital, Shanghai, 200233, China

    Zhenyuan Wei, Yang Zhao, Peichun Hsu, Shang Guo, Chi Zhang & Biao Zhong

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  1. Zhenyuan Wei
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  2. Yang Zhao
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  3. Peichun Hsu
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  4. Shang Guo
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  5. Chi Zhang
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  6. Biao Zhong
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Contributions

ZYW and YZ planned and executed experiments and wrote the manuscript, PCH composed figures and analyzed results, SG and CZ critically reviewed the manuscript, BZ oversaw the project, critically reviewed and edited the manuscript. All authors have read and approved the manuscript.

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Correspondence to Biao Zhong.

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Wei, Z., Zhao, Y., Hsu, P. et al. Exosomes for gene therapy effectively inhibit the endothelial-mesenchymal transition in mouse aortic endothelial cells. BMC Musculoskelet Disord 22, 1000 (2021). https://doi.org/10.1186/s12891-021-04896-0

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Keywords

BMC Musculoskeletal Disorders

ISSN: 1471-2474

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