- Open Access
Preparation and characterization of small-diameter decellularized scaffolds for vascular tissue engineering in an animal model
- Shuangyue Xu1, 2,
- Fangna Lu†1, 2,
- Lianna Cheng†1, 2, 7,
- Chenglin Li1, 2,
- Xu Zhou3,
- Yuan Wu4,
- Hongxing Chen3,
- Kaichuang Zhang6,
- Lumin Wang1, 2,
- Junjie Xia1, 2,
- Guoliang Yan1, 2, 5Email author and
- Zhongquan Qi1, 2Email author
© The Author(s) 2017
- Received: 28 December 2016
- Accepted: 28 April 2017
- Published: 11 May 2017
The development of a suitable extracellular matrix (ECM) scaffold is the first step in vascular tissue engineering (VTE). Synthetic vascular grafts are available as an alternative to autologous vessels in large-diameter arteries (>8 mm) and medium-diameter arteries (6–8 mm). In small-diameter vessels (<6 mm), synthetic vascular grafts are of limited use due to poor patency rates. Compared with a vascular prosthesis, natural tissue ECM has valuable advantages. Despite considerable progress in recent years, identifying an optimal protocol to create a scaffold for use in small-diameter (<6 mm) fully natural tissue-engineered vascular grafts (TEVG), remains elusive. Although reports on different decellularization techniques have been numerous, combination of and comparison between these methods are scarce; therefore, we have compared five different decellularization protocols for making small-diameter (<6 mm) ECM scaffolds and evaluated their characteristics relative to those of fresh vascular controls.
The protocols differed in the choice of enzymatic digestion solvent, the use of non-ionic detergent, the durations of the individual steps, and UV crosslinking. Due to their small diameter and ready availability, rabbit arteria carotis were used as the source of the ECM scaffolds. The scaffolds were subcutaneously implanted in rats and the results were evaluated using various microscopy and immunostaining techniques.
Our findings showed that a 2 h digestion time with 1× EDTA, replacing non-ionic detergent with double-distilled water for rinsing and the application of UV crosslinking gave rise to an ECM scaffold with the highest biocompatibility, lowest cytotoxicity and best mechanical properties for use in vivo or in situ pre-clinical research in VTE in comparison.
- Blood vessel decellularization
- Arterial tissue engineering
- Rabbit arteria carotis
Over 600,000 vascular grafts are implanted annually to replace damaged blood vessels, along with a considerable number of cardiac valves [1, 2]; therefore, there is increasing need to develop a tissue-engineered blood vessel substitute for use in cardiovascular tissue engineering [2, 3]. Despite rapid progress in recent years [2, 4], the critical factors to be overcome in vascular tissue engineering (VTE) technology are the same as those in other organ tissue engineering techniques; namely, selecting a suitable scaffold, seeding cells into it, and optimizing the microenvironment to ensure autonomous development of body-compatible tissue . So far, the priorities in VTE have been identifying an ideal material for the scaffolds, finding the most suitable sources for seeding cells, and perfecting in vitro culturing conditions to create an optimal tissue-engineered vascular graft (TEVG).
The first TEVG was developed by Weinberg and Bell  in 1986 using collagen gels to construct a scaffold onto which endothelial cells, fibroblasts and smooth muscle cells were added. Since then, a series of artificial materials have been used to produce scaffolds for clinical trials [6–9]: Synthetic materials have achieved some success in replacing larger coronary vessels (6–10 mm in diameter) ; however, in vessels with diameters <6 mm, thrombotic events have rapidly led to the vessels being closed off [11, 12]. For smaller diameter arteries (typically, 3–4 mm) physicians have almost exclusively relied on autologous vein grafts (e.g. saphenous vein) [4, 13, 14]. Therefore, intense research is being conducted to create clinically acceptable, small diameter vascular prostheses as alternatives to autologous arterial or venal excisions, especially in cardiovascular bypass surgery .
In order to perform VTE in human patients, it is of utmost importance that physicians, scientists, regulators and engineers work in concert to ensure the safety and well-being of human subjects enrolled in clinical trials. The most impressive results to date have been achieved by using fully natural TEVGs ; however, research to find a suitable extracellular matrix (ECM) scaffold for these types of grafts continues . Some research has reported using porcine, goat and bovine tissue for TEVGs with diameters of 4–6 mm [6, 17, 18]. However, studies on ECMs for use in blood vessels <2 mm in diameter are limited [15, 19–23], and reports on the effectiveness of different decellularization protocols are not abundant enough [20, 24–26]. For vessels in this size range, research has focused on the use of high molecular weight synthetic materials [27–30]. To achieve this, we selected rabbit arteria carotis, as opposed to synthetic materials, as the source of our scaffolds. The decellularization process is a compromise and balance between removal of cellular material and maintenance of the ECM. Further, considering the rationales for using different decellularization agents and their effects [17, 31], we conducted a series of tests to compare five different decellularization protocols and characterized the resulting scaffolds to identify an optimal method for creating an ECM scaffold with good mechanical properties and high biocompatibility for use in pre-clinical research.
Animals, harvesting of vascular samples and implantation of decellularized scaffolds
The animals were obtained from Xiamen University Animal Center. All the animals were anesthetized prior to extraction or implantation of vessels and scaffolds, and were humanely euthanized after the procedures were completed. The animal experiments were approved by the Animal Center of Xiamen University (Xiamen, China) and complied with the Instructive Notions with Respect to Caring for Laboratory Animals, 2006, published in by the Science and Technology Department of China.
Carotid arteries (20–40 mm in length with lumen diameters of 1.8–2.2 mm) were harvested from New Zealand white rabbits (male; 6 months old; weight, 2.0–2.5 kg). Warm ischemic time between tissue extraction to processing or storage at −20 °C was <1 h. Excess connective tissue was removed from the adventitia of the carotid arteries with a scalpel prior to decellularization.
Once decellularized, the scaffolds (length: 5 mm) were subcutaneously implanted into Sprague–Dawley rats (male; 4–6 weeks-old; weight 150 g). We used the suture line (6-0, PERMA-HAND Silk Suture; ETHICON INC., USA) which was used for locating the scaffolds as well as a maker to identify them when they were harvested. We implanted four samples in one group/rat at a spacing of 1.5 cm from each other. We harvested at the correct time point and maintained the samples of one group in the same background. For each set, we repeated this procedure thrice. The grafts were harvested on days 7, 14, 28 and 56 after implantation for histological examination and biocompatibility analysis. C57/B6 spleens were used as positive controls (Additional file 1: Figure S3) for in vivo studies, which are related to the immunofluorescent staining images shown in Fig. 4.
Decellularization of vascular-scaffolds
Experimental details for the five different decellularization protocols
Soaking in ddw for 24 h
Frozen at −80 °C and thawed twice
Soaking: 75% ethanol
Solvent:tissue ratio: 20:1 (v/w)
Total duration: 72 h
Solvent replacement at 1, 3, 6, 12, 24, 72 h
Soaking in ddw for 24 h
Digestion on an orbital shaker using a tissue:enzyme ratio (g/ml) of 1:15
PBS washing for 30 min; shaking
DNase and RNase for 6 h; shaking
Ultraviolet irradiation for 30 min
Scanning electron microscopy (SEM)
The scaffolds were prepared for scanning electron microscopy (SEM) by fixing in 2.5% glutaraldehyde for 2 h followed by dehydration through a graded series of ethanol concentrations. The scaffolds were immersed in pure tert-butyl alcohol (TBA) overnight and air-dried for 24 h. The scaffolds were sputter-coated with gold prior to visualization using a JEOL JSM-6390LV SEM (Jeol; Japan).
The decellularized scaffolds from each group were harvested from the rats 7, 14, 28 and 56 days after implantation. The samples were washed in normal saline and fixed in 4% paraformaldehyde for 24 h before being dehydrated through a graded series of ethanol. The samples were then embedded in paraffin and sliced into 5 μm-thick sections. For histological identification of cellular material, the sections were stained with hematoxylin and eosin (H&E), 4,6-diamidino-2-phenylindole (DAPI), Masson’s trichrome (Maxim Inc.; China) or Picrosirius red (Microherb Inc.; China).
Immunofluorescent staining was performed using biotin conjugated anti-mouse CD3e and CD11b (1:250, 2 µg/ml, eBioscience; San Diego, CA, USA) primary antibodies, followed by streptavidin-HRP, goat-anti-mouse Alexa Fluor 488 (1:1000, 2 µg/ml, Invitrogen; Carlsbad, CA, US) secondary antibodies. DAPI was used as a nuclear counterstain. The stained samples were visualized using a Motic BA310 microscope and analyzed by Motic Image Advanced 3.2. software (Motic Asia; China). The thicknesses of the intima & media membranes were also measured.
MTS cell proliferation assay
The MTS cell proliferation assay was performed using a CellTiter 96 AQueous One Solution Cell Proliferation Assay System (Promega; Madison, WI, USA). Briefly, the scaffolds were cultured in Dulbecco’s Modified Eagle Medium Nutrient Mixture F-12 (DMEM/F12) at 37 °C for 24 h at a density of 2.5 ml/cm2. The culture media (leach liquor) were collected and preserved. Human umbilical vein endothelial cells (HUVEC; ATCC; Rockville, MD, USA) were cultured to logarithmic phase, plated in 96-well plates (500 cells/well) and cultured for a further 24 h. The media were replaced with leach liquor from the scaffold cultures diluted with DMEM/F12 at the following ratios of 1:2, 1:4 and 1:8. The cells were cultured for a further 1, 3 and 5 days at 37 °C and their ODs were measured at 490 nm. A negative control was prepared using DMEM/F12 alone. The cytotoxicity of each protocol was evaluated by calculating the relative growth rate (RGR) [RGR = (mean OD for each group)/(mean OD of the negative control) × 100%] to determine the proliferation index. The evaluation standard was derived from the Biological evaluation of medical devices-Part 5: Test for in vitro cytotoxicity (GB/T 16886.5-2003/ISO 10993-5:1999, IDT).
Mechanical testing of scaffolds
Burst-pressure testing of the scaffolds
Decellularized scaffolds (approximately 10 mm in length) were randomly selected from each group. Each scaffold was attached via tapered adapters directly into a pressurized tube. The burst pressures were measured by delivering normal saline from a 50 ml syringe via a control valve. The fluid pressure (mbar) was monitored using a manometer with a data acquisition system (RM6240BT; Chengdu Science Instrument Factory; China). The system was progressively and manually pressurized until fluid was observed erupting from the vessel. This was defined as vessel failure or the burst pressure.
Testing suture retention strength of the scaffolds
Suture strength was measured using a magnetic base three-dimensional micro thruster and data acquisition system (STW-2 and RM6240BT, respectively; Chengdu Science Instrument Factory) following the manufacture’s instructions. Briefly, vascular samples, approximately 20 mm in length, were chosen randomly; 5-0 polypropylene sutures were placed in each side of the scaffold (1 mm from the edge) and constant elongation (2 mm/s) was applied along the longitudinal axis of the scaffold until the sutures were pulled through the vessel edge; the maximum suture strength was then recorded. The procedure was repeated in each of the five experimental groups and the results were compared to the suture retention strength of the negative control.
GraphPad Prism v. 5.0 software (GraphPad Inc.; San Diego, CA, USA) was used for all the statistical analyses. Data were expressed as mean ± SD. One-way analysis of variance (ANOVA) was performed to test for statistical differences. The burst-pressure test, suture retention test and intima & media thickness measurements were repeated three times in each group. The figures show the results from the final trials. A p value <0.05 was considered statistically significant.
Overall appearances of the scaffolds
Histological analysis of the decellularized scaffolds
The cross-sections of the scaffolds in each group were examined by H&E staining (Fig. 2; [13–18]) and DAPI staining (Fig. 2; [19–24]). Although nuclear residue was still evident in the control group (Fig. 2; ), almost no nuclear material was visible in the five decellularized scaffolds. This was confirmed though DNA content analysis (Additional file 1: Figure S1).
Masson’s trichrome staining and picrosirius red staining revealed that the pores in each of the experimental scaffolds were intersected with small collagen fibers resulting in small pore sizes, with tight packing of the large collagen-fiber network and elastin layers, producing a tight, dense matrix (Fig. 2; [25–36]). Blue showed collagen and elastin in the scaffolds upon Masson’s trichrome staining. Dark-red showed collagenous fibers in the scaffolds with picrosirius red staining.
Burst pressure testing of decellularized scaffolds
In general, the burst pressures of the decellularized scaffolds in the experimental groups were greater than those in the control group; however none of the differences were significant (Fig. 1C). The greatest differences were observed between groups IV and V versus the control group, both of these groups had been subjected to UV crosslinking. Conversely, a small, non-significant decrease was observed in the burst pressure of the scaffolds in group III compared to the control vessels.
Suture retention strength of the scaffolds
The retention strength of the sutures prior to implantation was not statistically different to that recorded in native rabbit carotid arteries, suggesting that the vascular graft scaffold had sufficient suture retention strength to withstand anastomotic forces. Suture retention analysis between the groups revealed significant differences in the retention strengths in the decellularized scaffolds in groups II, IV and V compared to those in the control group (Fig. 1D; p < 0.01), especially in groups IV and V (p < 0.001).
Biocompatibility of decellularized scaffolds in vitro and in vivo
Cytotoxicity of the decellularized scaffolds in vitro
Evaluation of scaffold cytotoxicity in vitro for each protocol
OD value (mean ± SD)
1.239 ± 0.04
0.967 ± 0.02
1.093 ± 0.05
0.897 ± 0.03
0.957 ± 0.04
0.747 ± 0.01
Host cell infiltration and integration of the decellularized scaffolds in vivo
Most research into TEVG has focused on the use of macromolecular synthetic materials, such as PGA [20, 21], polycaprolactone , polypropylene carbonate (PPC) , and electrospun tecophilic/gelatin nanofibers . However, these yielded unsatisfactory long-term patency due to thrombotic failure in small-diameter vessels (<6 mm). The decellularized natural matrices took advantage of structure and mechanical performance, while avoiding adverse immunological reactions due to their origin . As a consequence, research has increasingly been directed toward the suitability of fully natural vascular materials and ECM scaffolds prepared from blood vessels extracted from animals or human subjects [7, 9, 18, 35–39]. By combining these types of scaffolds with seeding cells obtained from the patient (autologous stem cells or endothelial cells), the TEVG forms an xenograft that has less thrombogenicity than synthetic materials and the characteristics required to promote cell attachment, migration and proliferation. Several groups have successfully developed xenogeneic bioprosthetic valves consisting of chemically crosslinked, intact porcine aortic valves, or valves created from crosslinked bovine pericardial tissue [40–42]; however, none of these methods have achieved vascular scaffolds with diameters ≤2 mm. In this study, we selected rabbit arteria carotis as the source of ECM scaffolds as these vessels have diameters of ~ 2 mm. Compared with using vessels from ovines [18, 43] and canines [24, 37], rabbits are easier to get and cost less; moreover, the vessel diameter of rabbits is nearly 2 mm, compared with around 4–6 mm from ovines and canines. Thus, rabbit is a suitable animal model for evaluation research of TEVG.
Initially, we prepared the scaffolds according to the protocol of Zhao et al. .; however, these achieved limited success, possibly due to a failure in fully removing cellular contamination, or due to factors associated with the surface active agent, rinse step, temperatures or durations, or because the rabbit arteria carotis was smaller than that from sheep. Furthermore, we considered the different effects of physical, chemical and biological agents and the convenience of operation in the laboratory setting . With regard to physical agents, the temperature was the initial choice, which operated as freezing and thawing for several cycles. With respect to chemical agents, non-ionic detergents such as Triton X-100  are more effective than ionic detergents such as deoxycholate [45, 46]. Meanwhile, biological agents (as pepsin, DNase and RNase) are commonly used for decellularization agent but must be followed by rinsing. Currently, a combination of several agents is popular in the decellularization process to avoid single side effects for only one agent . Finally, we compared five different decellularization protocols using combinations of the agents mentioned above to identify the one that produced the cleanest ECM scaffold, with good mechanical properties, biocompatibility and minimal cytotoxicity, which are the combined potential beneficial effects of biological scaffolds. Each protocol differed in the digestion conditions for cell removal, rinsing conditions (non-ionic detergent vs. ddw) and whether the sample was subjected to UV irradiation to promote crosslinking, meanwhile avoiding potential cytotoxicity . Even though we chose the agents, it remained difficult to ensure the concentration and time for each agent. As reported in our pilot experiment , we decided that the common sections were: (1) freezing at −80 °C and thawing twice; (2) soaking in 75% ethanol as mentioned in Table 1; (3) PBS washing for 30 min with shaking between pepsin and nucleases, (4) operation at 4 °C all the time. We set up different sections for each group: group I, 0.125% pepsin in commercial EDTA solvating agent (defined as 1× EDTA)/1.5 h shaking; group II, 2× EDTA/1 h shaking; group III 1× EDTA/2 h shaking and rinsing only in Triton X-100, not ddw; group IV 1× EDTA/2 h shaking and rinsing in ddw, addition of ultraviolet irradiation for 30 min; group V, 2× EDTA/1.5 h shaking and rinsing as group III, addition of ultraviolet irradiation for 30 min.
A negative control was prepared by immersing a fresh vascular sample in ddw throughout the protocol. DNase and RNase soaking for 6 h was sufficient for nucleic acid removal. Therefore, there was no different among experimental groups in terms of full infiltration, as reported previously [25, 38, 48].
Examination of the resulting scaffolds by SEM and histological microscopy showed there was little difference between the five protocols in relation to cellular residue. The ECMs prepared through protocols III and V showed the least smooth outer surfaces and rupture or tenuity of collagen could be observed according to Fig. 1B. Even both these protocols involved Triton X-100 in the rinsing step, we concluded that Triton X-100 could be a break factor for collagen structure and its cytotoxicity. This was confirmed by examining the intima and media through Masson’s trichrome and Picrosirius red staining. Furthermore, protocols III and V resulted in the highest levels of cytotoxicity (level 2), indicating that these scaffolds were unsuitable for clinical use. In contrast, the cytotoxicity of the remaining scaffolds (groups I, II and IV) was low (level 1) relative to the cytotoxicity in the control group. We speculated that the increased cytotoxicity in groups III and V was also a consequence of the Triton X-100 detergent. We could discard these two protocols for consideration. Preservation of the intima and media is important for the maintenance of cell function in decellularized scaffolds [20, 24, 26, 49]. Of the other three protocols, protocol IV yielded the tightest and least broken ECM structure with the thickest intima and media according to the SEM and breadth in Fig. 1B. The suture retention strengths of ECM scaffolds determine whether the grafts can withstand the forces exerted by anastomosis. The mechanical properties of the scaffolds were evaluated via burst pressure and suture retention strength tests. Testing of the burst pressure was in agreement with the results of Zhao et al. . Although there were no statistically significant differences in the burst pressures between the experimental groups (Fig. 1C), there were significant differences in suture retention strength between groups II, IV and V and that of the control group. The differences were greatest with protocols IV and V (p < 0.001); whereas, protocol III showed the worst performance in both tests.
In order to establish whether decellularized scaffolds prepared from rabbit carotid arteries had sufficiently low immunogenicity for xeno-implantation, and thereby the ability to enhance tissue ingrowth in vivo, subcutaneous implantation of the decellularized scaffolds was performed in Sprague–Dawley rats and the results were examined through immunohistochemical staining. We observed a progressive reduction in inflammatory reactions between the experimental groups and the control group. The biodegradability of vascular scaffolds is a critical factor in their clinical suitability [49–51]. We found that after 56 days, the ECM scaffolds in groups II, IV and V had nearly disappeared and could only be recognized by their suture points; in contrast, the infiltration of inflammatory cells in group I and the control group was clearly evident. Degradation of the scaffolds was fastest in groups IV and V, both of which had undergone UV crosslinking reactions. We had discarded group III and V, so we finally obtained the protocol of group IV by comparison.
In combination, the findings suggested that the use of Triton X-100 in the rinsing step (III and V) and increasing the concentration of EDTA in the digestion step (II and V) both led to an increase in the pore size of the matrix; however, this effect could be reversed by crosslinking through UV irradiation (IV and V). This was consistent with a previous study carried out using porcine carotid arteries . Overall, protocol IV appeared to be the most effective method for creating an ECM substitute for use in small-diameter cardiovascular vessels <2 mm. To confirm the biocompatibility of the scaffold prepared through this protocol, we employed CD3e and CD11b as markers for T cells and macrophage cells, respectively, by immunofluorescence (Fig. 4). In relation to CD3e (T cells), the results showed a clear reduction in the immunoreactivity of this scaffold compared to that in the control group, demonstrating that protocol IV possessed superior biocompatibility. Also, we observed that the T cells only embraced the scaffolds, with few inside, which may suggest that the immunological reaction was still activated. While there was also a reduction in the level of CD11b (macrophages), however the difference was small, and it showed that the marked cells in the control group were distributed compared with those in group IV. However, in group IV, the cells embraced the boundary of the scaffold, possibly due to the critical roles of macrophages in neovascularization and adipogenesis [49, 50, 53]. Of note, was the observation that the macrophages in group IV were localized around the scaffolds, indicating greater immigration; whereas no such localization was observed in the control group. Actually, it would be better to obtain all of the groups immunostaining images. It’s a limitation of this study.
Apart from what has been discussed above, other factors can influence the decellularization process , such as physical factors (rocking/whirling/sonicating) or device procedural factors. We developed a simple combination for decellularization, but three-dimensional printing technology is growing fast . One of the limitations of our study was that we focused only on the preparation and characterization of small-diameter decellularized scaffolds as a common approach for pre-clinical research. More research must be done on the interaction between factors during decellularization.
The ultimate goal of our study was to develop a small-diameter TEVG using a decellularized ECM scaffold sourced from rabbit carotid arteries which could be used as a model for pre-clinical research. Five protocols were tested and compared, each differing in the enzymatic digestion and rinsing conditions and the duration of the individual steps: the non-ionic detergent, Triton X-100 increased their cytotoxicity; however, suture strength could be rescued through UV crosslinking; and the rate of scaffold degradation could be increased by altering the concentration of EDTA used in enzymatic digestion.
Overall, in the five groups of this research, protocol IV produced a decellularized ECM scaffold with the highest biocompatibility, lowest cytotoxicity and the best mechanical properties. Hence, we provided a suitable protocol to make a small-diameter vessel scaffold model for preclinical research.
SX main operator, Ph.D. candidate, who gives the main idea, and the whole design, in charge of SEM and the decellularization of vascular-scaffolds. FL main operator, master, in charge of the HE staining, co-operating the decellularization of vascular-scaffolds. LC main operator, master, in charge of the other stainings, co-operating the decellularization of vascular-scaffolds. CL in charge of the MTS cell proliferation assay. XZ, YW, KZ, LW help preparing the vascular. JX help modify the manuscript. GY the giude of mechanical testing of scaffolds. ZQ acquisition of the financial support for the project leading to this publication. All authors read and approved the final manuscript.
The authors would like to thank Ms. Ping CHEN (School of Life Sciences, Xiamen University), Hongliu QIAN (Medical College, Xiamen University), and Yilin ZHAO (Department of Vascular Surgery, Xiamen University Affiliated Zhongshan Hospital) for their technical support. We also thank Yilin ZHAO, Zhiyong ZHANG (School of Medicine, Shanghai Jiao Tong University, Shanghai 9th People’s Hospital), and Yang XU (University of California, San Diego) for their discussions on the manuscript. We espeicilly thank Dr. Yang Xu for his recommendation and accepting Shuangyue Xu (the first author) as visiting student to perform immunofluorescent staining in his laboratory. We are grateful to the native English speaking scientists of Elixigen Company (Huntington Beach, California) for editing our manuscript.
The authors declare that they have no competing interests.
Availability of data and materials
Data sharing not applicable to this article as no datasets were generated or analysed during the current study.
Ethics approval and consent to participate
All the animals were anesthetized prior to extraction or implantation of vessels and scaffolds, and were humanely euthanized after the procedures were completed. The animal experiments were approved by the Animal Center of Xiamen University (Xiamen, China) and complied with the Instructive Notions with Respect to Caring for Laboratory Animals, 2006, published in by the Science and Technology Department of China.
This study was approved by the Ethics Committee of Xiamen University with the Permit Number XMULAC20120093.
This work was supported by the National Natural Science Foundation of China (No. 31271038), and the Major State Scientific Research Program of China (No. 2012CBA01303).
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