Morini · Journal of anatomy 2007 · Animal experimental study · n=?

Revascularization and remodelling of pancreatic islets grafted under the kidney capsule.

Cited 57 times in the scientific literature.

Level 5 - mechanism / opinion, no new human data

Animal model (preclinical mouse study)

PubMed 17394557 · doi:10.1111/j.1469-7580.2007.00717.x · record verified 2026-08-26

What was done

Pancreatic islets isolated from donor mice were transplanted under the kidney capsule of syngeneic diabetic recipient mice. Graft-bearing kidneys were harvested at sequential time points post-transplantation and analyzed using light microscopy, immunohistochemistry (including BrdU staining to detect proliferation), and transmission electron microscopy. Investigators performed quantitative morphometry comparing the proportions and distribution of alpha, beta, and delta cells between native and grafted islets, and monitored graft function via time to diabetes reversal and intraperitoneal glucose tolerance testing.

What was found

Recipient mice reversed diabetes within 4 days post-transplant. Blood vessel ingrowth from host cortical and capsular networks initiated at days 4–7, with vessel morphology resembling native islets by days 7–14. Quantitative analysis demonstrated statistically significant differences in both the proportions and spatial organization of alpha, beta, and delta cells compared with intact native islets (exact percentages not reported in abstract). No beta-cell proliferation was detected by BrdU staining.

Why it matters

This study demonstrates that although subcapsular islet grafts rapidly revascularize and restore glycemic control in mice, the remodeled endocrine architecture differs fundamentally from native islets. This altered structural organization may provide a morphological basis for the impaired secretory dynamics often observed after clinical islet transplantation.

Limits

The abstract does not report the total number of animals, precise numerical values for cell proportions, or glycemic/IPGTT data points. Findings from a syngeneic murine model under the renal capsule may not fully translate to human islet transplantation, which typically uses intraportal infusion in an allogeneic setting.

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