Cell scaffold constructs
The present invention relates to the regeneration, reconstruction, repair, augmentation or replacement of organs or tissue structures using scaffolds and autologous cells that are not derived from such organs or tissues.
1. An implantable construct for replacement of a defective bladder in a human subject comprising
a) a tubular scaffold having a first open end configured for anastomosis to an opening in the subject's abdominal wall, a second open end configured to connect to a ureter; and
b) an autologous cell population that is not derived from the defective bladder, deposited on or in a surface of the tubular scaffold,
wherein the cell population is a smooth muscle cell population derived from adipose tissue or peripheral blood, and wherein the implantable construct is adapted for temporary storage and passage of urine.
2. The implantable construct of claim 1 , wherein the first open end is configured to connect to an abdominal wall section.
3. The implantable construct of claim 1 , wherein the first open end is configured to form a stoma.
4. The implantable construct of claim 1 , wherein the first open end is configured to be positioned flush with the abdominal wall.
5. The implantable construct of claim 1 , wherein the first open end is configured to be sutured to the skin of the subject.
6. The implantable construct of claim 1 , wherein the first open end is configured to be anastomosed to the skin.
7. The implantable construct of claim 3 , wherein the stoma further comprises a stoma button.
8. The implantable construct of claim 1 , wherein the tubular scaffold further comprises a side opening configured to connect to a second ureter.
9. The implantable construct of claim 1 , wherein the biocompatible scaffold is biodegradable.
10. The implantable construct of claim 1 , wherein the scaffold comprises a material selected from the group consisting of polyglycolic acid, polylactic acid, and a copolymer of polyglycolic acid and polylactic acid.
11. The implantable construct of claim 1 , wherein the diversion is free of urothelial cells.
12. The implantable construct of claim 1 , wherein the smooth muscle cell (SMC) population is not derived from in vitro differentiation of mesenchymal stem cells (MSCs).
13. The implantable construct of claim 1 , wherein the tubular scaffold is coated with a biocompatible and biodegradable shape-setting material.
14. The implantable construct of claim 13 , wherein the shape-setting material comprises a poly-lactide-co-glycolide copolymer.