Tissue-engineered constructs
View Patent ↗The present invention provides constructs including a tubular biodegradable polyglycolic acid scaffold, wherein the scaffold may be coated with extracellular matrix proteins and substantially acellular. The constructs can be utilized as an arteriovenous graft, a coronary graft, a peripheral artery bypass conduit, or a urinary conduit. The present invention also provides methods of producing such constructs.
1. A method of producing a tubular construct comprising:
(a) providing a tubular biodegradable polyglycolic acid (PGA) construct having an inner diameter of about 3 mm to about 6 mm, wherein the tubular PGA construct comprises entangled PGA fibers, wherein the density of the PGA is about 45 mg/cc to about 75 mg/cc, and wherein said density is uniform across the entire tubular PGA construct,
(b) seeding human cells at passage 6 or less on the tubular biodegradable polyglycolic acid construct,
(c) culturing the cells under conditions such that the cells secrete extracellular matrix proteins on the tubular biodegradable polyglycolic acid construct, wherein the cells are cultured in medium comprising about 11% to about 30% human serum for the first 2-6 weeks of culture and in medium comprising about 1% to about 10% human serum for at least an additional 4 weeks,
(d) decellularizing the construct in step (c) such that the construct is substantially acellular comprising less than 5% intact cells and wherein the construct is intimal hyperplasia and calcification resistant, and
(e) degrading the polyglycolic acid construct in step (c) such that the polyglycolic acid comprises less than 33% of the cross-sectional area of said construct, and wherein the construct has an extracellular matrix protein thickness greater than about 200 μm at the thinnest portion of the construct, thereby producing a decellularized tubular construct.
2. The method of claim 1 , wherein the decellularizing step occurs in the absence of sodium dodecyl sulfate (SDS).
3. The method of claim 1 , wherein the decellularizing step employs an endonuclease.
4. The method of claim 1 , wherein the construct is substantially acellular comprising less than 1% intact cells.
5. The method of claim 1 , wherein the cells are isolated from human aorta.
6. The method of claim 1 , wherein the cells comprise smooth muscle cells.
7. The method of claim 1 , wherein the medium in step (c) further comprises high glucose, insulin, bFGF and EGF.
8. The method of claim 1 , wherein the cells are at seeded onto the tubular biodegradable polyglycolic acid construct at about 0.5×10 6 cells per cm length of construct to about 2×10 6 cells per cm length of construct.
9. The method of claim 1 , wherein the seeded cell and the seeded cells' progeny, collectively produce greater than 1 ng of hydroxyproline per cell over 9 weeks in culture.
10. The method of claim 1 , wherein step (a) further comprises scouring the tubular PGA construct to remove heavy metal contaminants.
11. The method of claim 10 , wherein the heavy metal contaminant is selected from the group consisting of aluminum, barium, calcium, iodine, lanthanum, magnesium, nickel, potassium and zinc.
12. A method of producing a tubular construct comprising:
(a) providing a tubular biodegradable polyglycolic acid (PGA) construct having an inner diameter of about 3 mm to about 6 mm and scouring the tubular PGA construct to remove heavy metal contaminants, wherein the tubular PGA construct comprises entangled PGA fibers, wherein the density of the PGA is about 45 mg/cc to about 75 mg/cc, and wherein said density is uniform across the entire tubular PGA construct,
(b) seeding human cells at passage 6 or less on the tubular biodegradable polyglycolic acid construct,
(c) culturing the cells under conditions such that the cells secrete extracellular matrix proteins on the tubular biodegradable polyglycolic acid construct,
(d) decellularizing the construct in step (c) such that the construct is substantially acellular comprising less than 5% intact cells and wherein the construct is intimal hyperplasia and calcification resistant, and
(e) degrading the polyglycolic acid construct in step (c) such that the polyglycolic acid comprises less than 33% of the cross-sectional area of said construct, and wherein the construct has an extracellular matrix protein thickness greater than about 200 μm at the thinnest portion of the construct, thereby producing a decellularized tubular construct.
13. The method of claim 12 , wherein the decellularizing step occurs in the absence of sodium dodecyl sulfate (SDS).
14. The method of claim 12 , wherein the decellularizing step employs an endonuclease.
15. The method of claim 12 , wherein the construct is substantially acellular comprising less than 1% intact cells.
16. The method of claim 12 , wherein the cells are isolated from human aorta.
17. The method of claim 12 , wherein the cells comprise smooth muscle cells.
18. The method of claim 12 , wherein the cells are cultured in medium comprising about 11% to about 30% human serum for the first 2-6 weeks of culture and in medium comprising about 1% to about 10% human serum for at least an additional 4 weeks.
19. The method of claim 12 , wherein the medium further comprises high glucose, insulin, bFGF and EGF.
20. The method of claim 12 , wherein the cells are at seeded onto the tubular biodegradable polyglycolic acid construct at about 0.5×10 6 cells per cm length of construct to about 2×10 6 cells per cm length of construct.
21. The method of claim 12 , wherein the seeded cell and the seeded cells' progeny, collectively produce greater than 1 ng of hydroxyproline per cell over 9 weeks in culture.
22. The method of claim 12 , wherein the heavy metal contaminant is selected from the group consisting of aluminum, barium, calcium, iodine, lanthanum, magnesium, nickel, potassium and zinc.