Bioartificial pancreas transplantation at prevascularized intermuscular space: effect of angiogenesis induction on islet survival

Pancreas. 2003 Apr;26(3):279-85. doi: 10.1097/00006676-200304000-00012.

Abstract

Introduction: Bioartificial pancreas (BAP) transplantation offers a potential treatment of diabetes mellitus. The optimal site for BAP transplantation has not yet been established.

Aim: To monitor the effect of induction of neovascularization at the intermuscular space on islet survival after allogenic transplantation of BAP.

Methodology: Angiogenesis was induced at the intermuscular space of diabetic Lewis rats by implanting a polyethylene terephthalate (PET) mesh bag, which enclosed a collagen sponge and biodegradable gelatin microspheres containing basic fibroblast growth factor. After confirmation of angiogenesis, BAP was prepared by mixing of 5% agarose with approximately 2,800 isolated rat (Sprague-Dawley) islets and transplanted into the prevascularized PET mesh bag.

Results: Neovascularization was observed in and around the PET mesh bag within 10 days after implantation as confirmed by macroscopic and microscopic examinations. In the presence of a collagen sponge, new blood vessels penetrated into the PET mesh bag and formed a vascular bed. After transplantation, normoglycemia was achieved in the rats within 3 days and maintained for >35 days. The rats gradually gained body weight, and the results of intravenous glucose tolerance test showed normal patterns of blood glucose clearance 1 month after transplantation.

Conclusion: It can be concluded that the prevascularized PET mesh bag enabled transplanted BAP to survive and maintain function, thus indicating a potential site for BAP transplantation.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / analysis
  • Body Weight
  • Cell Survival / drug effects
  • Fibroblast Growth Factor 2 / pharmacology
  • Glucose Tolerance Test
  • Islets of Langerhans Transplantation / methods*
  • Male
  • Neovascularization, Physiologic*
  • Pancreas / blood supply*
  • Pancreas / drug effects
  • Pancreas, Artificial*
  • Polyethylene Terephthalates
  • Rats
  • Rats, Inbred Lew
  • Rats, Sprague-Dawley

Substances

  • Blood Glucose
  • Polyethylene Terephthalates
  • Fibroblast Growth Factor 2