doi: 10.1161/CIRCULATIONAHA.107.757369
(Circulation. 2008;118:S52-S57.)
© 2008 American Heart Association, Inc.
Myocardial Protection, Perioperative Management, and Vascular Biology |
Bioengineered Three-Layered Robust and Elastic Artery Using Hemodynamically-Equivalent Pulsatile Bioreactor
From the Laboratory for Tissue Engineering and Regenerative Medicine (K.I., K.K., S.K., A.C.P., M.C., C.A.V.), Brigham and Women’s Hospital, Harvard Medical School, Boston, Mass; Waseda Institute for Advanced Study (K.I.), Tokyo, Japan; the Institute for Biomedical Engineering, Consolidated Research Institute for Advanced Medical Care (K.I., M.U.), Waseda University, Tokyo Japan; and the Major in Integrative Bioscience and Biomedical Engineering (M.U.), Graduate School of Waseda University, Tokyo, Japan.
Correspondence to Koji Kojima, Laboratory for Tissue Engineering and Regenerative Medicine, Brigham and Women’s Hospital, Harvard Medical School. 75 Francis Street, Thorn 1327, Boston, MA 02115. E-mail kojima{at}zeus.bwh.harvard.edu
 |
Abstract |
|---|
 Top Abstract IntroductionMethodsResultsDiscussionReferences |
|---|
Background— There is an essential demand for tissue engineered autologous small-diameter vascular graft, which can function in arterial high pressure and flow circulation. We investigated the potential to engineer a three-layered robust and elastic artery using a novel hemodynamically-equivalent pulsatile bioreactor.
Methods and Results— Endothelial cells (ECs), smooth muscle cells (SMCs), and fibroblasts were harvested from bovine aorta. A polyglycolic acid (PGA) sheet and a polycaprolactone sheet seeded with SMCs, and a PGA sheet seeded with fibroblast, were wrapped in turn on a 6-mm diameter silicone tube and incubated in culture medium for 30 days. The supporting tube was removed, and the lumen was seeded with ECs and incubated for another 2 days. The pulsatile bioreactor culture, under regulated gradual increase in flow and pressure from 0.2 (0.5/0) L/min and 20 (40/15) mm Hg to 0.6 (1.4/0.2) L/min and 100 (120/80) mm Hg, was performed for an additional 2 weeks (n=10). The engineered vessels acquired distinctly similar appearance and elasticity as native arteries. Scanning electron microscopic examination and Von Willebrand factor staining demonstrated the presence of ECs spread over the lumen. Elastica Van Gieson and Masson Tricrome Stain revealed ample production of elastin and collagen in the engineered grafts. Alpha-SMA and calponin staining showed the presence of SMCs. Tensile tests demonstrated that engineered vessels acquired equivalent ultimate strength and similar elastic characteristics as native arteries (Ultimate Strength of Native: 882±133 kPa, Engineered: 827±155 kPa, each n=8).
Conclusions— A robust and elastic small-diameter artery was engineered from three types of vascular cells using the physiological pulsatile bioreactor.
Key Words: arteries • elasticity • vascular grafts
|
Introduction |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Atherosclerotic vascular diseases such as coronary artery and peripheral vascular disease represent a significant cause of mortality in the United States1 (www.americanheart.org, Heart Disease and Stroke Statistics 2007 Update, American Heart Association). 1.4 million arterial bypass operations are annually performed in the United States2; however, approximately 100 000 patients requiring small-caliber arteries have no suitable autologous vein or arteries.3 Numerous studies have been done to develop thrombo-resistant and life-long lasting synthetic vascular grafts. Unfortunately, because of poor antithrombogenicity and inconsistent material property,4 clinical outcomes of synthetic vascular grafts with an inner diameter of less than 6 mm are not satisfactory.5 Five recent randomized, controlled trials of superficial femoral artery stenting failed to demonstrate any benefit of a stainless-steel stent over angioplasty alone, and the stented arteries had a restenotic rate over 70% at one year.6,7 Therefore, there is an essential demand for tissue-engineered autologous small-diameter arteries. The feasibility of tissue engineering blood vessels was demonstrated in low-pressure pulmonary outflow tracts in pediatric patients.8,9 Recently, blood vessels engineered from autologous fibroblast-derived tissues extracted from skin biopsies were endothelialized and clinically translated to adult human arterial revascularization.10,11 The tissue engineering of 3-layered, elastic, and small-diameter arteries with antithrombogenicity is still a major unrealized challenge.8–13 We have developed a physiological pulsatile bioreactor system which can regulate pressure, flow circulation, the concentration of carbon dioxide, and the pH of the circulating culture medium. In an effort to study whether elastic and robust blood vessels could be devised, we bioengineered a vascular conduit using a hemodynamically-equivalent pulsatile bioreactor system.
|
Methods |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Cell Isolation and Culture
Calf aortas of 2 to 14 days old were obtained from a local slaughterhouse within 5 hours of sacrifice. Small branch vessels were tied with sutures (Prolene 3 to 0, Ethicon), and the tissues were rinsed several times with phosphate buffered saline (PBS; Invitrogen) containing 100 U/mL penicillin G sodium, 100 µg/mL streptomycin sulfate, and 0.25 µg/mL amphotericin B (Antibiotic-Antimycotic, Invitrogen). For isolation of endothelial cells (ECs), one end of the aorta was clamped and M199 medium (Invitrogen) containing 0.2% collagenase type I (Worthington Biochemical) and Antibiotic-Antimycotic were injected into the aortic lumen. Both the ends of aorta were clamped. After a 25-minute incubation at 37°C in a humid atmosphere with 5% carbon dioxide (5% CO2 incubator, Thermo Fisher Scientific), the cell solution was centrifuged. The resulting cell pellet was suspended in M199 medium containing 10% Fetal Bovine Serum (FBS, Invitrogen), Antibiotic-Antimycotic, and 25 µg/mL L-ascorbic acid (Sigma). ECs were expanded in a CO2 incubator. The identity of ECs was confirmed by a cobblestone appearance and by subsequent positive staining for von Willebrand factor in the engineered vessels. After isolation of the ECs, the medial layer was dissected free from the adventitia and minced into 2 mmx2 mm pieces. For isolation of smooth muscle cells (SMCs), the medial tissues were digested in 0.2% collagenase type I diluted in DMEM (Invitrogen) containing Antibiotic-Antimycotic at 37°C for 12 hours on a shaker. The cell suspension was passed through a sterile 100-µm nylon cell strainer (Becton Dickinson), and the filtrate was centrifuged. The cell pellet was suspended in DMEM containing 20% Ham’s F12 medium (Invitrogen), 10% FBS, Antibiotic-Antimycotic, and 25 µg/mL L-ascorbic acid, and expanded in a CO2 incubator. The identity of SMCs was confirmed by a "hill and valley" appearance, and by subsequent positive staining for
smooth muscle actin ( SMA) and calponin in the medial layer of the tissue engineered vessels. For fibroblast isolation, the adventitia was separated from the medial layer and was minced into 2 mm x2 mm pieces. The tissue segments were digested and fibroblasts were expanded in the same manner.
Biodegradable Polymer Templates
Nonwoven meshes of polyglycolic acid (PGA) fibers with 14-µm diameter (Concordia Fibers) were used as templates for seeding SMCs and fibroblasts. Polycaprolactone porous sheets were fabricated. Sucrose-containing (Sigma) distilled water was embedded into a mold of 4 cmx8 cmx2 mm and dried. The sucrose mold was dipped into a solution of 3% polycaprolactone (Sigma) dissolved in methylene chloride (Sigma). The mold was dried overnight, and the subsequent polycaprolactone was trimmed into a sheet measuring 2.5 cmx6 cmx0.4 mm.
Construction of a Vessel Structure
A PGA sheet of 3 cmx6 cmx0.1 mm and a polycaprolactone sheet of 2.5 cmx6 cmx0.4 mm were seeded with SMCs. In 4 days of incubation in a CO2 incubator, the PGA sheet associated with SMCs was wrapped on a silicone tube (Figure 1), and placed in a T75 flask (Becton Dickinson) supplemented with DMEM containing 20% Ham’s F12 medium, 10% FBS, Antibiotic-Antimycotic, and 25 µg/mL L-ascorbic acid. This flask was placed in a CO2 incubator on an orbital shaker (New Brunswick Scientific), which provided gentle agitation. After 3 days of incubation, the PCL sheet with SMCs was overwrapped. After another 3 weeks of incubation, a PGA mesh sheet that had been seeded with fibroblasts 2 days before was overwrapped on the incubated tubular tissue and continuously incubated for another 2 days. The luminal supporting silicone tube was removed, and the tubular polymer-cell construct was mounted on a specially-designed chamber. Half a million ECs suspended in M199 containing 25 mmol/L HEPES (Invitrogen), 10% FBS, Antibiotic-Antimycotic, and 25 µg/mL L-ascorbic acid were injected into the lumen, and the outer area in the chamber was filled with the same culture medium without ECs. The chamber was placed on the shaker in a CO2 incubator for 2 days. Throughout the incubation period, culture medium was exchanged every day.
|
A Novel Bioreactor Design
The pulsatile bioreactor consists of a left ventricular model,14 synthetic polymer-made mitral and aortic valves,15 a compliant silicone tube, a peripheral resistive unit, a gas exchange unit, and a chamber to mount the engineered vessel (Figure 2). Pulsatile circulation can be generated by the left ventricular model which is pneumatically driven by positive and negative pressure. In the bioreactor, there is main flow through the tissue-engineered vessel as well as subflow that passes through the outside of the vessel. The subflow was regulated by a tubing pump (As One). Heart rate and systolic fraction are adjustable within 40 to 210 bpm and 10% to 90%, respectively, by a computer-controlled system. Dynamic flow and pressure waveforms can be regulated within physiological conditions. Pressure and flow applied to the engineered vessels were measured by a pressure transducer (UK-801, Edwards Lifesciences) and by an electromagnetic flow probe (FF-180T, Nihon Kohden). Throughout a long-term culture period, pressure and flow can be gradually changed to simulate the growth process from fetus to adult. The gas, in the concentration of 10% carbon dioxide and 10% oxygen, was supplemented into the circulating culture medium (DMEM containing 20% Ham’s F12 medium, 10% FBS, Antibiotic-Antimycotic, and 25 µg/mL L-ascorbic acid) through the gas exchange unit, which resulted in the circulating medium containing 5% carbon dioxide in a pH range of 7.41 to 7.42.
|
Pulsatile Bioreactor Culture
The pulsatile bioreactor culture was performed for 14 days (n=10). Heart rate and systolic fraction were regulated to 70 bpm and 34%, respectively. The culture period for 14 days was divided into 5 periods (Figure 2), and pulsatile flow and pressure were regulated to be gradually increased from a mean flow rate of 0.2 (0.5/0) L/min and mean pressure of 20 (40/15) mm Hg to eventually 0.6 (1.4/0.2) L/min and 100 (120/80) mm Hg (Figure 2). The circulating culture medium was exchanged once every 7 days.
Histological Examinations
Tissue samples were fixed in 10% formalin, embedded in paraffin, and sectioned. With standard histological techniques, samples were stained with hematoxylin and eosin, Masson Tricrome, and Elastica Van Gieson.
Immunohistochemical Examinations
For immunohistochemical staining, 7- to 10-µm-thick frozen sections were used. For endothelial detection, rabbit antihuman von Willebrand factor (DAKO) diluted in PBS (1:20) was used as a primary antibody. As a secondary antibody, goat antirabbit IgG-Cy3 (1:20, Jackson ImmunoResearch Laboratories) was used followed by 4,6-diamino-2-phenylindole (DAPI, 1 mg/mL, Sigma) nuclear staining. For -SMA staining, mouse antihuman smooth muscle actin (1:20, DAKO) was used as a primary antibody, rabbit antimouse IgG-Cy3 (1:20, Jackson ImmunoResearch Laboratories) was used as a secondary antibody, and DAPI was used for nuclear staining. For calponin staining, mouse antihuman calponin (1:20; Sigma) was used as a primary antibody, and rabbit antimouse IgG-FITC (1:20, Jackson ImmunoResearch Laboratories) was used as a secondary antibody, and propidium iodide (1 mg/mL, Sigma) was used for nuclear staining.
Scanning Electron Microscopic Examinations
Tissue samples were fixed with 2.5% glutaraldehyde in phosphate buffer (pH 7.2). The samples were postfixed in 1% phosphate buffered tannic acid for 2 hours, and 1% phosphate buffered OsO4 for 1.5 hours, dehydrated with 10-minute exchanges in each of 50%, 70%, 80%, 90% aqueous ethanol solution, and 3 times in absolute ethanol. The dried samples were sputter-coated with platinum palladium, and examined with a scanning electron microscope (S-2500CX, Hitachi, Tokyo, Japan).
Mechanical Properties
Mechanical properties of the tissue-engineered blood vessels were examined using a uni-axial tensile tester (AG-I 250kN, Shimadu). Tissue-engineered vessels as well as native arteries were cut in circumferential direction and opened. Tissue specimens, 3 mm in width and 7 mm in length, were tested in a humid condition, under a tissue-extension rate of 10 mm/min. Ultimate strength and ultimate strain were investigated for the tissue engineered vessels, the native arteries, and the polymer scaffolds. Elastic modulus of each collagen and elastin region were investigated for the tissue engineered vessels and the native arteries.
Statistical Analysis
The experimental data of mechanical properties were expressed as mean±SD. The assumptions of equality of variances and normal distribution of errors were checked for all the variables obtained. Then, for the comparison of ultimate strength and ultimate strain among the three groups, the statistical analyses were performed using the Kruskall-Wallis test, and statistical significance of differences (P<0.05) was further examined by the Steel-Dwass test. A Student t test was used to compare the elastic modulus of the elastin and collagen regions between the 2 groups. A probability value of <0.05 was considered to be statistically significant.
The authors had full access to and take full responsibility for the integrity of the data. All authors have read and agree to the manuscript as written.
|
Results |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
The Novel Physiological Pulsatile Bioreactor Culture Produced Elastic Blood Vessels
After a total of 46 days in vitro culture of bovine vascular cells (ECs, SMCs, and fibroblasts) associated with biodegradable polymers (PGA and PCL), including dynamic bioreactor culture for 2 weeks under gradual increase in pulsatile pressure and flow (Figure 2), the engineered vessels acquired distinctly similar appearance to native vessels (Figure 3A and 3B). The bioreactor culture induced homogeneous tubular tissue generation in the engineered vessels. When a compression force was applied and removed from the engineered vessels, the round lumen shape of the engineered vessels was immediately recovered. Cyclic deformation of the engineered vessels was followed by cyclic forces (supplemental movie). It has been confirmed that the engineered vessels occupied a striking elasticity, which was one of the key issues in tissue engineering blood vessels.
|
Construction of Morphologically Similar Bioengineered Vessels Using a Technique of Cell-Polymer Sheet Wrapping Followed by the Novel Bioreactor Culture
The engineered vessels consist of integration of a PGA mesh sheet seeded with SMCs, a PCL porous sheet seeded with SMCs, a PGA sheet seeded with fibroblast, and ECs seeded on the lumen. Hematoxylin and eosin staining showed that the engineered vessels consist of a dense muscle region in the middle layer and loosely formed outer region (Figure 4A). The spaces inside of the engineered vessels denoted where polycaprolactone exists (Figure 4A, 4C, 4D, and 4E). The degradation period of polycaprolactone is around 1 to 2 years. Morphologically endothelial-like cells were present in the lumen (Figure 4B). Smooth-muscle-like cells were observed just beneath the endothelial-like cells. Elastica Van Gieson staining and Masson Tricrome staining demonstrated the presence of abundant elastin in the middle layer of the bioengineered vessels (Figure 4C and 4D) as well as production of well-organized collagen extracellular matrix (Figure 4E and 4F). The luminal area of the engineered vessels was positive for von Willebrand factor (Figure 5), demonstrating the presence of endothelial cells. The medial layer was positive for -SMA and calponin (Figure 5B and 5C), indicating the presence of SMCs. Scanning electron microscopic examinations demonstrated that ECs were present and spread over the lumen, and that ECs were morphologically organized along with flow direction (Figure 6). Dynamic pressure and flow circulation in the bioreactor culture was gradually increased, and eventually regulated to the conditions of aortic circulation of 6-mm diameter artery, as pulsatile pressure of 120/80 mm Hg, and pulsatile flow of 1.4/0.2 L/min. The data demonstrated that the bioreactor culture preserved attachment of ECs in the lumen throughout 2 weeks of pulsatile bioreactor culture, including under actual aortic circulation.
|
|
|
Bioengineered Blood Vessels Acquired Mechanically Equivalent Strength and Elasticity to Native Arteries
The tissue samples were obtained in circumferential direction. The stress-strain behaviors of the biodegradable polymer scaffolds alone differed distinctly from those of native arteries (Figure 7A and 7B). The stress-strain behaviors of the engineered vessels were quite similar to those of native arteries (Figure 7A and 7B), indicating that the bioreactor culture contributed to create morphologically similar tissues to native arteries. Ultimate strength, ultimate strain, and elastic modulus of each collagen and elastin region were obtained from the stress-strain curves of native arteries, bioengineered vessels, and polymer scaffolds. Because biodegradable polymers do not have tissue components, the elastic modulus of each elastin and collagen region was excluded from the comparison. It was demonstrated that the engineered vessels acquired equivalent mechanical strength to native arteries (Figure 7C, each n=8, native: 882±133 kPa, engineered: 827±155 kPa). It was also revealed that the engineered vessels acquired robust strength 9 times higher than polymer templates (polymers: 91±21 kPa). There was difference in ultimate strain between native arteries and the engineered vessels (Figure 7D, P<0.05); however, the ultimate strain of the engineered vessels, indicating extension ability, reached 70% of native arteries. It was demonstrated that the elastic modulus of collagen region were equivalent between native arteries and the engineered vessels (Figure 7E, each n=8, native: 3.31±0.56 MPa, engineered: 3.75±0.78 MPa). Elastic modulus of elastin region of the engineered vessels was slightly higher as compared with that of native arteries. The results indicated that although ample amount of elastin was produced in the engineered vessels (Figure 4D), the amount of elastin did not reach that of native arteries.
|
|
Discussion |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
We have developed the physiological pulsatile flow and pressure bioreactor system to enhance the growth of tissue-engineered vessels (Figure 2). The bioreactor system is able to regulate flow, pressure, heart rate, and systolic fraction, and possibly produce dynamic circulations from vein to artery and from fetus to adult. Concentration of carbon dioxide was regulated to 5%, and the pH in the circulated culture medium was maintained at 7.4
7.42. Although in vivo mechanical functional behavior of native arteries is mainly governed by elastin and activated SMCs at physiological pressure,16 the previous distinguished studies of engineered vessels were deficient in elastin production and engineered vessels had little elasticity.3,8–13 This is the first report showing the development of bioengineered arteries that acquired ample amounts of elastin as well as unprecedented elasticity (Figure 4D and Supplemental movie). The tensile tests demonstrated that the bioengineered vessels acquired equivalent robustness and similar elasticity in comparison to native arteries (Figure 7). Elastin production in the bioengineered vessels was slightly lower than native arteries. We demonstrated how to bioengineer robust, elastic, and 3-layered arteries using 3 types of vascular cells (ECs, SMCs, and fibroblast), using the technique to wrap cell-polymer sheets on a silicone tube to form a tubular layered structure (Figure 1). This was accomplished by using the novel pulsatile bioreactor which can produce physiological circulations. ECs were present in the lumen, and activated SMCs were confirmed by calponin staining and observed in the middle layer of the bioengineered vessels (Figures 5 and 6
). Presence of ECs spread over the lumen and production of elastin in the bioengineered vessels indicated that the bioreactor can grow and maintain blood vessels (Figures 4 through 6). Because ECs were present under a real aortic pulsatile circulation, it is considered that those ECs have a strong potential possibility to be worked in vivo without any loss by high shear flows after implantation. Although further studies should be addressed, the bioreactor presented here has the potential to incubate and preserve tissues and organs. As the diffusional supply of oxygen can support only 100- to 200-µm-thick tissues,17 one of the major challenges in tissue engineering remains to construct 3-D thick and functional tissues. The thickness of engineered vessel walls has been reached to 668±90 µm (n=8). This is the first report to demonstrate the growth of the thick engineered vessels constructed from ECs, SMCs, and fibroblasts in vitro. Our subsequent studies will address the feasibility of maintaining the bioengineered vessels in arterial circulation in vivo. Because the tissue-engineered vessels were grown in actual arterial pressure and flow environments in vitro, the vessels should have a strong potential to function in in vivo arterial circulation. It is recognized that the mismatch in material properties between the synthetic vascular grafts and native vessels is one of the major causes inducing occlusion as well as restenosis.4 The fact that mechanical properties such as the elastic modulus for collagen and elastin regions, ultimate strength, and ultimate strain are almost consistent between the tissue engineered vessels and the native arteries, and that the lumen of the engineered vessels were endothelialized before implantation, will contribute to the enhancement of proper regeneration. It is anticipated that the regions of polycaprolactone and polyglycolic acid in the tissue engineered vessels will be matured in vivo by circulating progenitor cells18,19 as well as host cells that have migrated from the anastomosed sites. We believe that the immature area will have an important role in guiding regeneration and integration between the bioengineered and the native arteries. Carotid artery replacement with the tissue engineered vessels, constructed from autologous cells harvested from internal mammary artery, will be performed to demonstrate the feasibility in a large animal model. As cell sources for engineering vessels, bone marrow cells20 and endothelial progenitor cells21 will be examined. Further studies will be performed to investigate whether the bioreactor has a potential to differentiate bone marrow cells to vascular specific cells.
|
Acknowledgments |
|---|
Sources of Funding
This study was partly supported by the Establishment of Consolidated Research Institute for Advanced Science and Medical Care, Encouraging Development Strategic Research Centers Program, the Special Coordination Funds for Promoting Science and Technology, Ministry of Education, Culture, Sports, Science and Technology, Japan, and by Grant-in-Aid for Scientific Research Japan (Young Scientists (B) 17790956).
Disclosures
None.
|
Footnotes |
|---|
Presented at the American Heart Association Scientific Sessions, November 4–7, 2007, Orlando, Fla.
The online Data Supplement can be found with this article at http://circ.ahajournals.org/cgi/content/full/CIRCULATIONAHA.107.757369/DCI.
|
References |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
1. Ross R. The pathogenesis of atherosclerosis: a perspective for the 1990s. Nature. 1993; 362: 801–809.[CrossRef][Medline] [Order article via Infotrieve]
2. Langer R, Vacanti JP. Tissue engineering. Science. 1993; 260: 920–926.
3. Mckee JA, Banik SS, Boyer MJ, Hamad NM, Lawson JH, Niklason LE, Counter CM. Human arteries engineered in vitro. EMBO Rep. 2003; 4: 633–638.[CrossRef][Medline] [Order article via Infotrieve]
4. Nerem RM, Ensley AE. The tissue engineering of blood vessels and the heart. Am J Transplant. 2004; 4 (suppl6): 36–42.[CrossRef][Medline] [Order article via Infotrieve]
5. Meinhart JG, Deutsch M, Fischlein T, Howanietz, Fröschl A, Zilla P. Clinical autologous in vitro endothelialization of 153 infrainguinal ePTFE grafts. Ann Thorc Surg. 2001; 71 (suppl5): S327–S331.[CrossRef][Medline] [Order article via Infotrieve]
6. Schillinger M, Sabeti S, Loewe C, Dick P, Amighi J, Mlekusch W, Schlanger O, Cejna M, Lammer J, Minar E. Balloon angioplasty versus implantation nitinol stents in the superficial femoral artery. N Engl J Med. 2006; 354: 1879–1888.
7. Capek P, McLean GK, Berkowitz HD. Femoropopliteal angioplasty. Factors influencing long-term success. Circulation. 1991; 83 (Suppl 2): I70–I80.[Medline] [Order article via Infotrieve]
8. Shin'oka T, Imai Y, Ikada Y. Transplantation of a tissue-engineered pulmonary artery. N Engl J Med. 2001; 344: 532–533.
9. Shin'oka T, Matsumura G, Hibino N, Naito Y, Watanabe M, Konuma T, Sakamoto T, Nagatsu M. Kurosawa H. Midterm clinical result of tissue-engineered vascular autografts seeded with autologous bone marrow cells. J Thorac Cardiovasc Surg. 2005; 129: 1330–1338.
10. L'Heureux N, Dusserre N, Konig G, Victor B, Keire P, Wight TN, Chronos NA, Kyles AE, Gregory CR, Hoyt G, Robbins RC, McAllister TN. Human tissue engineered blood vessels for adult arterial revascularization. Nat Med. 2006; 12: 361–365.[CrossRef][Medline] [Order article via Infotrieve]
11. L'Heureux N, Pâquet S, Labbé R, Germain L, Auger FA. A completely biological tissue-engineered human blood vessel. FASEB J. 1998; 12: 47–56.
12. Niklason LE, Gao J, Abbott WM, Hirschi KK, Houser S, Marini R, Langer R. Functional arteries grown in vitro. Science. 1999; 284: 489–493.
13. Klinger RY, Blum JL, Hearn B, Lebow B, Niklason LE. Relevance and safety of telomerase for human tissue engineering. Proc Natl Acad Sci U S A. 2006; 103: 2500–2505.
14. Iwasaki K, Umezu M, Iijima K, Inoue A, Imachi K, Ye CX. Development of a polymer bileaflet valve to realized a low-cost pulsatile blood pump. Artif Organs. 2003; 27: 28–83.
15. Iwasaki K, Umezu M, Abe Y, Chinzei T, Isoyama T, Saito I, Ishimaru M, Imachi K. The improved jellyfish valve: durability enhancement with sufficient blood compatibility. ASAIO J. 2002; 48: 532–537.[CrossRef][Medline] [Order article via Infotrieve]
16. Armentano RL, Levenson J, Barra JG, Fischer EI, Breitbart GJ, Pichel RH, Simon A. Assessment of elastin and collagen contribution to aortic elasticity in conscious dogs. Am J Physiol. 1991; 260: H1870–H1877.[Medline] [Order article via Infotrieve]
17. Carmeliet P, Jain RK. Angiogenesis in cancer and other diseases. Nature. 2000; 407: 249–257.[CrossRef][Medline] [Order article via Infotrieve]
18. Shi Q, Rafii S, Wu MH, Wijelath ES, Yu C, Ishida A, Fujita Y, Kothari S, Mohle R, Sauvage LR, Moore MAS. Evidence for circulating bone marrow-derived endothelial cells. Blood. 1998; 92: 362–367.
19. Thakahashi T, Kalla C, Masuda H, Chen D, Silver M, Kearney M, Magner M, Isner JM, Asahara T. Ischemia- and cytokine-induced mobilization of bone marrow-derived endothelial progenitor cells for neovascularization. Nat Med. 1999; 5: 434–438.[CrossRef][Medline] [Order article via Infotrieve]
20. Matsumura G, Miyagawa-Tomita S, Shin'oka T, Ikada Y, Kurosawa H. First evidence that bone marrow cells contribute to the construction of tissue-engineered vascular autografts in vivo. Circulation. 2003; 108: 1729–1734.
21. Kaushal S, Amiel GE, Guleserian KJ, Shapira OM, Perry T, Sutherland FW, Rabkin E, Moran AM, Schoen FJ, Atala A, Soker S, Bischoff J, Mayer JE Jr. Functional small-diameter neovessels created using endothelial progenitor cells expanded ex vivo. Nat Med. 2001; 7: 1035–1040.[CrossRef][Medline] [Order article via Infotrieve]
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||