Extraction and cultivation of endothelial progenitor cells
Endothelial progenitor cells (EPCs) have been extracted and cultivated utilizing the entire bone marrow adherent methodology. Bone marrow was remoted from the femurs of 3-week-old feminine rabbits and transferred to a sterile 15 mL centrifuge tube. The tube was centrifuged at 800 rpm for five min, and the supernatant was discarded. The pellet was then resuspended in Dulbecco’s Modified Eagle Medium/Nutrient Combination F-12 (DME/F12, Hyclone, USA) tradition medium supplemented with 10% fetal bovine serum (Gibco, USA). The cell tradition bottle was positioned in a CO2 incubator at 37 °C with a 5% CO2 ambiance for 20 h. Subsequently, non-adherent cells have been collected by centrifugation at 800 rpm for five min and resuspended in EBM-2MV tradition medium (Lonza, Basel, Switzerland). The cells have been transferred to a brand new cell tradition bottle and continued to be cultured within the CO2 incubator to acquire EPCs. The tradition medium was changed each 48 h to acquire second-generation cells for subsequent characterization.
Extraction of endothelial progenitor cell-derived exosomes
The cells have been cultured till reaching a density of 70–80%, after which the medium was changed with exosome-depleted serum tradition medium for an extra 2 days of cultivation. Afterward, the tradition supernatant was collected right into a 50 mL centrifuge tube. The collected supernatant was subjected to centrifugation to take away cell particles and different massive particles. Centrifugation was carried out utilizing a Beckman Coulter centrifuge at 2000 × g for 20 min to take away cell particles, adopted by centrifugation at 10,000 × g for 30 min, and eventually at 100,000 × g for 120 min. After centrifugation, the pellet was resuspended in 15 mL of PBS (Servicebio, Chian). The suspension was filtered by means of a 0.22 μm pore-sized membrane filter to take away residual cell particles and different impurities, acquiring a purer supernatant. Lastly, the filtrate was centrifuged at 4000 × g to acquire a 200 µL pellet for subsequent experiments.
Measurement of exosome particle measurement
The exosomes have been transferred to centrifuge tubes and diluted with PBS buffer, making certain thorough mixing of the pattern to attain a homogeneous suspension. A Malvern particle measurement analyzer was arrange in keeping with the producer’s directions. The pattern was transferred to the pattern chamber of the Malvern particle measurement analyzer, making certain the cleanliness of the pattern chamber and avoiding any air bubbles that would have an effect on the measurement outcomes. Applicable parameters have been set primarily based on the instrument’s necessities and the character of the pattern for particle measurement measurement. The particle measurement distribution of the exosomes was analyzed by measuring the depth of sunshine scattered by the pattern. For nanoparticle monitoring evaluation (NTA) of exosome measurement, exosome samples have been ready following the identical process as with the Malvern particle measurement analyzer. Exosome samples have been collected from the tradition supernatant and transferred to centrifuge tubes. The pellet was resuspended utilizing a buffer answer (PBS) and ensured thorough mixing of the pattern. In keeping with the producer’s directions, the pattern was injected into the pattern chamber of the NTA instrument. Laser energy and digital camera publicity time have been adjusted primarily based on the pattern’s properties and instrument necessities. The instrument robotically captured and tracked the movement trajectories of the exosomes and analyzed their measurement and focus primarily based on their Brownian movement. After the exosomes have been mounted with glutaraldehyde, their morphology and particle measurement have been analyzed utilizing transmission electron microscopy (TEM, Hitachi, Japan).
Preparation of decellularized extracellular matrix (dECM)
New Zealand rabbits have been euthanized, and their tracheas have been instantly harvested. The connective tissue on the outer wall of the trachea was meticulously eliminated, and the contemporary trachea was then lower into small fragments. The fragments underwent an intensive washing with PBS answer, adopted by immersion in sterile deionized water at 4 °C for twenty-four h. Subsequently, the fragments have been incubated in an answer containing 0.25% Triton X-100 and 0.25% sodium deoxycholate (SD) at 37 °C for twenty-four h. After the incubation interval, the fragments have been rinsed with sterile distilled water for 30 min after which incubated in a 1 M NaCl answer containing 1 kU/mL DNase I (Sigma, USA) and a pair of U/mL RNase (Sigma, USA) for twenty-four h. Your entire course of was carried out in a constant-temperature shaking incubator at 37 °C, set to a velocity of 60 revolutions per minute. Following the incubation, the fragments underwent a 72-hour washing course of with sterile deionized water, with water being modified each 12 h. The washed tracheal fragments have been subsequently frozen at -80 °C for twenty-four h after which subjected to freeze-drying in a vacuum freeze dryer for twenty-four h. After the freeze-drying course of, the ensuing dried dECM particles have been floor utilizing liquid nitrogen. The bottom particles have been then filtered by means of a chrome steel mesh till they may go by means of fully. Lastly, the bottom and filtered dECM powder was transferred into tubes and saved at -20 °C for future use.
Preparation of GMN-dECM-Exos hydrogel scaffold
To organize the GMN-dECM-Exos hydrogel, 0.15 g/mL GelMA and 0.04 g/mL Nanoclay have been added to PBS buffer and stirred at room temperature till totally dissolved. A magnetic stirrer was employed to facilitate the dissolution course of. The combination was then heated to 50℃ and stirring was continued till full dissolution. Subsequently, the dECM freeze-dried powder was added to the answer to attain a 5% focus. Subsequent, 50 µg of exosomes per milliliter of answer was added and stirred at 37℃till totally dissolved. The pH of the answer was measured utilizing a pH meter and adjusted to pH 7. The dissolved answer was then filtered by means of a 0.22 μm filter membrane to acquire a transparent hydrogel answer. The filtered answer was transferred right into a mildew, and a photoinitiator, 0.25% (w/v) lithium acylphosphinate photo-initiator (LAP, EFL, China), was added for crosslinking. The scaffold underwent speedy seen light-induced crosslinking with an irradiation depth of 11mW/cm2 for a period of 1 min.
Detection of porosity
The scaffold is vacuum-dried to fixed weight, and its dry mass Wd is measured. Subsequently, the scaffold is positioned in anhydrous ethanol with a identified density ρe to make sure full protection. It’s soaked for twenty-four h to permit the ethanol to totally permeate the scaffold’s pores, after which the moist weight Ww is measured. The scaffold is then eliminated, and any residual ethanol on the floor is gently blotted away, adopted by measuring its moist mass W w. The quantity of the scaffold is V, and the porosity P(%) is calculated as:
$$:Pleft(%proper)=(Ww-Wd)/rho e:Vtimes:100%$$
Biomechanical analysis of scaffolds
The biomechanical properties of varied scaffolds have been assessed utilizing a common testing machine (AGS-X, Shimadzu Company, Japan). Every group consisted of three samples (n = 3). The chosen scaffold samples underwent measurements utilizing a vernier caliper to find out their size, thickness, outer diameter, and inside diameter. These dimensional parameters have been meticulously recorded. Subsequently, the scaffold samples have been subjected to compression testing on the common testing machine. Incremental hundreds have been step by step utilized till the purpose of most deformation or failure of the scaffold was reached. The corresponding most load worth and elastic modulus have been recorded at this vital stage.
Stay/lifeless staining assay
For the Stay/Useless Staining Assay, cells have been instantly cultured on the floor of the biomaterial. After a 3-day incubation interval, the classy cells have been handled with Calcein AM (Beyotime, China) and incubated at 37 °C for 30 min. Subsequently, propidium iodide dye (Sigma, USA) was added, adopted by a 10-minute incubation at 4 °C in the dead of night. Fluorescence microscopy was then used to seize photographs for commentary.
Western blot
Exosomes have been remoted from the tradition medium of endothelial progenitor cells by means of ultracentrifugation. Subsequently, the exosome samples diluted in PBS have been collected and dissolved in RIPA protein extraction buffer to launch proteins. Protease and phosphatase inhibitors have been added to protect protein integrity. The protein focus of the extracted vesicles was decided utilizing a BCA protein assay equipment (Thermo, USA). An acceptable gel focus, resembling 10–15% SDS-PAGE gel, was chosen primarily based on protein measurement and goal protein molecular weight. The vesicle protein pattern was combined with protein loading buffer, heated, and loaded into gel wells. Following electrophoresis, proteins have been transferred onto a PVDF or nitrocellulose membrane utilizing a moist switch system. The membrane was then incubated in blocking buffer, adopted by incubation with major and secondary antibodies. After washing, the membrane was developed utilizing chemiluminescent reagents (Thermo, USA).
DNA quantification
Genomic DNA was extracted from contemporary and decellularized tracheal samples utilizing the Genomic DNA Purification Package (Shenergy Biocolor, Shanghai, China). Briefly, 50 mg of dry tissue was floor in liquid nitrogen and digested in a buffer containing proteinase Ok at 55℃ for 3 h. The combination was centrifuged at 12,000 rpm for five min at room temperature, and the supernatant was collected. After including 300µL of answer B, the pattern was combined and centrifuged once more beneath the identical situations. Following three washing steps to take away contaminants, DNA was eluted in 100µL of Tris-EDTA answer. The DNA focus was quantified by measuring absorbance at 260 nm and 280 nm utilizing a microplate reader (Epoch, BioTek, USA).
Move cytometry
EPCs have been harvested on the second passage (P2), washed with phosphate-buffered saline (PBS), and resuspended in a staining buffer. The cell suspension was incubated with fluorescence-conjugated antibodies: CD31/APC (Bioss, Beijing, China), CD34/PE (Genetex, SC, USA), CD45/PE (Bioss, Beijing, China), and CD105/FITC (Genetex, SC, USA). Following incubation, the cells have been washed to take away unbound antibodies after which resuspended in PBS for evaluation. Information have been acquired utilizing a circulation cytometer and analyzed to establish the cell populations.
In vivo angiogenesis assay
The rooster chorioallantoic membrane (CAM) assay was employed as an in vivo mannequin to guage the angiogenic properties of the pattern teams [51]. Fertilized rooster eggs have been incubated beneath managed situations at a continuing temperature of 37.8 °C and humidity of 60%. On the eighth day of incubation, a window was created roughly 1 cm away from the embryo’s head on the CAM floor, marked by a pencil. After iodine disinfection, a central space of roughly 5 mm×5 mm was designated, and the eggshell and shell membrane have been meticulously eliminated utilizing ophthalmic forceps and scissors. Tissue samples measuring 2 mm×2 mm have been positioned within the avascular area between the 2 anterior vitelline veins, round 1 cm away from the embryo’s head. All procedures have been performed beneath sterile situations, and CAMs have been photographed every day for the next 4 days. The variety of blood vessels overlaying the grafts and the sponge was evaluated utilizing a picture analyzer to evaluate the angiogenic response.
Immunofluorescence staining
Paraffin-embedded sections have been deparaffinized and hydrated. Antigen retrieval was carried out by incubating the sections at 37℃ for 30 min in a 0.1% trypsin answer, adopted by rinsing with PBS. Extra floor water was gently faraway from the sections, and circles have been drawn across the tissue. Inside these circles, 5% bovine serum albumin (BSA) was utilized. The sections have been then incubated at 37℃in a humidified chamber for 30 min. Subsequently, the blocking answer was rigorously eliminated, and the pre-diluted major antibody was utilized to the sections. The sections have been positioned in a damp field with a small quantity of water and incubated in a single day at 4℃. The sections have been washed with PBS, after which the corresponding fluorescent secondary antibody was utilized inside the circles, overlaying the specimen tissue. The sections have been incubated at room temperature in the dead of night for 60 min after which washed with PBS. Subsequent, the DAPI staining answer (Solarbio, China) was added inside the circles, adopted by incubation at room temperature in the dead of night for two min. The sections have been washed with PBS and an acceptable quantity of anti-fade mounting agent was added. Lastly, coverslips have been utilized utilizing impartial resin. The sections have been noticed and pictures have been captured utilizing a fluorescence microscope.
Immunohistochemical staining commentary
The paraffin-embedded sections have been subjected to deparaffinization and hydration. Antigen retrieval was carried out by incubating the sections at 37℃for 30 min in a 0.1% trypsin answer, adopted by rinsing with PBS. A 3% hydrogen peroxide answer, serving as an endogenous peroxidase inhibitor, was added to the slides and allowed to incubate at room temperature for 10 min. Every slide was then handled with regular non-immune animal serum, a non-specific staining inhibitor, at room temperature for 10 min. Then the first antibody was utilized to the sections. The slides have been incubated in a single day at 4℃ adopted by washing with PBS. Subsequently, a biotinylated secondary antibody, particularly a biotin-labeled goat anti-rabbit IgG polymer, was added and incubated at 37℃ for 30 min. After one other spherical of PBS washing, the slides have been uncovered to a streptavidin-biotin-peroxidase advanced answer. The slides have been then processed for DAB staining (Solarbio, China) in keeping with the supplied directions, with a staining time starting from 30 s to 2 min. Following an 8-minute incubation with hematoxylin answer at room temperature, the slides have been rinsed with faucet water and counterstained with a bluing reagent. Subsequently, the sections have been dehydrated, cleared, mounted, and noticed beneath a microscope.
Tracheal scaffold implantation
New Zealand rabbits have been anesthetized through intravenous injection of two.5 mL/kg of 20% (w/v) ethyl carbamate (Aladdin, China), adopted by upkeep with isoflurane all through the surgical process. Following shaving and disinfection, an incision was made on the ventral midline of the neck caudal to the larynx. The neck muscle tissue have been rigorously dissected layer by layer, with meticulous separation of fascia and blood vessels to totally expose the trachea. A window defect measuring 5 mm in size and a pair of mm in width, involving two tracheal rings, was created roughly 2 cm under the cricoid cartilage. A tracheal scaffold measuring 6 mm in size and three mm in width was implanted on the web site, and the defect and scaffold have been secured utilizing 4 − 0 absorbable surgical sutures (Jinhuan, China) with interrupted suturing. After suctioning, the wound was closed in layers utilizing 3 − 0 silk sutures ((Jinhuan, China), and an area anesthetic (2% (w/v) lidocaine; Aladdin, China) was utilized across the wound web site. Postoperatively, the animals acquired an intramuscular injection of 8 million U/day penicillin G for 3 consecutive days to stop an infection. Lastly, tracheal samples have been collected following euthanasia of the rabbits through intravenous injection of an overdose of pentobarbital sodium (200 mg/kg). All animal experiments performed on this research have been authorised by the Ethics Committee of the Yangzhou College College of Medication.
Scanning Electron microscope (SEM) commentary
Recent tissue samples have been collected from every group and ready into 3 mm × 3 mm tissue blocks. The samples have been mounted in 2.5% glutaraldehyde at 4 °C for twenty-four h. After fixation, the samples underwent three washes with PBS, every lasting 15 min. Subsequently, the tissue samples have been dehydrated in a graded alcohol sequence for 10 min at every degree. The dehydrated samples have been then dried utilizing a vital level dryer (CPD-300, Leica, Germany) with CO2. The dried samples have been mounted with the commentary floor dealing with upward and affixed to a specimen holder. A skinny layer of gold was deposited on the pattern surfaces utilizing an ion sputtering instrument (SCD500, Bal-Tel, USA). Lastly, the samples have been examined and photographed utilizing a area emission scanning electron microscope (Gemini 300, Hitachi, Japan).
Statistical evaluation
Statistical evaluation was performed utilizing one-way evaluation of variance (ANOVA) or a two-tailed Scholar’s t-test, using GraphPad Prism 7 software program (San Diego, USA). Every experiment was replicated thrice, and the outcomes are reported as imply ± commonplace deviation.
