Novel vascular graft grown within recipient's own peritoneal cavity.

A method by which to overcome the clinical symptoms of atherosclerosis is the insertion of a graft to bypass an artery blocked or impeded by plaque. However, there may be insufficient autologous mammary artery for multiple or repeat bypass, saphenous vein may have varicose degenerative alterations that can lead to aneurysm in high-pressure sites, and small-caliber synthetic grafts are prone to thrombus induction and occlusion. Therefore, the aim of the present study was to develop an artificial blood conduit of any required length and diameter from the cells of the host for autologous transplantation. Silastic tubing, of variable length and diameter, was inserted into the peritoneal cavity of rats or rabbits. By 2 weeks, it had become covered by several layers of myofibroblasts, collagen matrix, and a single layer of mesothelium. The Silastic tubing was removed from the harvested implants, and the tube of living tissue was everted such that it now resembled a blood vessel with an inner lining of nonthrombotic mesothelial cells (the "intima"), with a "media" of smooth muscle-like cells (myofibroblasts), collagen, and elastin, and with an outer collagenous "adventitia." The tube of tissue (10 to 20 mm long) was successfully grafted by end-to-end anastomoses into the severed carotid artery or abdominal aorta of the same animal in which they were grown. The transplant remained patent for at least 4 months and developed structures resembling elastic lamellae. The myofibroblasts gained a higher volume fraction of myofilaments and became responsive to contractile agonists, similar to the vessel into which they had been grafted. It is suggested that these nonthrombogenic tubes of living tissue, grown in the peritoneal cavity of the host, may be developed as autologous coronary artery bypass grafts or as arteriovenous access fistulae for hemodialysis patients.

[1]  W. Roberts,et al.  Tension on coronary bypass conduits. A neglected cause of real or potential obstruction of saphenous vein grafts. , 1976, The Journal of thoracic and cardiovascular surgery.

[2]  J. Campbell,et al.  T lymphocytes affect smooth muscle cell phenotype and proliferation. , 1995, Arteriosclerosis, thrombosis, and vascular biology.

[3]  J. Hoying,et al.  The neointima formed in endothelial cell sodded ePTFE vascular grafts results from both cellular-hyperplasia and extracellular-hypertrophy. , 1996, Cell transplantation.

[4]  C. Mittermayer,et al.  Detection of minimal but significant amount of von Willebrand factor in human omentum mesothelial cell cultures. , 1996, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[5]  P. Mosse,et al.  A COMPARISON OF THE AVASCULAR CAPSULE SURROUNDING FREE FLOATING INTRAPERITONEAL BLOOD CLOTS IN MICE AND RABBITS , 1985, Pathology.

[6]  C. Remacle,et al.  Morphology and fibrinolytic activity of canine autogenous mesothelium used as venous substitute , 1986, Research in experimental medicine. Zeitschrift fur die gesamte experimentelle Medizin einschliesslich experimenteller Chirurgie.

[7]  G. Gabbiani,et al.  Myofibroblasts in an avascular fibrous tissue. , 1973, Laboratory investigation; a journal of technical methods and pathology.

[8]  G. Campbell,et al.  Venous Response to Endothelial Denudation , 1986, Pathology.

[9]  V. Bigl,et al.  Blot analyses and immunocytochemistry of neural antigens with digoxigenylated primary and secondary antibodies. , 1997, Brain research. Brain research protocols.

[10]  K. Bailey,et al.  Coronary restenosis: prospects for solution and new perspectives from a porcine model. , 1993, Mayo Clinic proceedings.

[11]  G. Campbell,et al.  ORIGIN OF MYOFIBROBLASTS IN THE AVASCULAR CAPSULE AROUND FREE‐FLOATING INTRAPERITONEAL BLOOD CLOTS , 1983, Pathology.

[12]  J. Sixma,et al.  Thrombomodulin activity on mesothelial cells: perspectives for mesothelial cells as an alternative for endothelial cells for cell seeding on vascular grafts , 1996, British journal of haematology.

[13]  R Langer,et al.  Functional arteries grown in vitro. , 1999, Science.