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Updated: Jun 5, 2026

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Scaffold-supported Transplantation of Islets in the Epididymal Fat Pad of Diabetic Mice
Published on: July 23, 2017
Nanofibrous Bioabsorbable Functionalized Scaffolds Augment Subcutaneous Islet Engraftment and Function in Mice
Purushothaman Kuppan1,2, Chelsea Castro1,2, Joy Paramor1,2
1Alberta Diabetes Institute, University of Alberta, Edmonton, Alberta, Canada.
Diabetes
|June 4, 2026
Summary
Bioabsorbable functionalized scaffolds (BAFS) create a vascularized subcutaneous niche for islet transplantation. These BAFS support long-term islet graft survival and improve diabetes management in mice.
Area of Science:
- Biomaterials Science
- Regenerative Medicine
- Endocrinology
Background:
- The subcutaneous space is a potential site for islet transplantation to treat type 1 diabetes.
- Developing a vascularized niche is crucial for successful islet engraftment and function.
Purpose of the Study:
- To evaluate nanofibrous bioabsorbable functionalized scaffolds (BAFS) for creating a vascularized subcutaneous niche to support islet transplantation.
- To assess the efficacy of BAFS in promoting vascularization and islet graft survival in a mouse model.
Main Methods:
- Electrospun poly(lactic-co-glycolic acid) and gelatin scaffolds functionalized with vascular endothelial growth factor and laminin were implanted in the subcutaneous space of mice.
- Vascularization was assessed by quantifying lectin, smooth muscle actin, and CD31 positive cells.
- Neonatal porcine islets were transplanted into diabetic mice with BAFS, and glycemic control was monitored.
Main Results:
- BAFS significantly enhanced vascularization in the subcutaneous space compared to control groups.
- Islet recipients with BAFS achieved normoglycemia faster and maintained higher serum porcine insulin levels.
- The BAFS supported long-term islet graft survival, indicating successful engraftment and function.
Conclusions:
- Nanofibrous BAFS effectively create a vascularized subcutaneous niche that supports islet engraftment and long-term function.
- This approach offers a promising and tunable alternative site for beta-cell replacement therapies in treating type 1 diabetes.

