Language

English

Publication Date

5-1-2025

Journal

Bioengineering & Translational Medicine

DOI

10.1002/btm2.10740

PMID

40385531

PMCID

PMC12079526

PubMedCentral® Posted Date

12-13-2024

PubMedCentral® Full Text Version

Post-print

Abstract

Revascularization plays a critical role in the successful engraftment of transplanted pancreatic islets, which are inherently rich in capillaries to meet their high metabolic demands. Innovative islet encapsulation strategies such as the NICHE (neovascularized implantable cell homing and encapsulation), generate a prevascularized transplantation site that allows for direct integration of the graft with the systemic circulation. Timing the transplantation is key to maximizing islet engraftment and survival, especially in diabetic individuals, who exhibit impaired wound healing. Therefore, in this study, we explored different methods to assess vascular development within NICHE in vivo in a non-invasive fashion. We effectively tracked neoangiogenesis using nanoparticle contrast-enhanced computed tomography (nCECT), observing a steady increase in vascularization over an 8-week period, which was confirmed histologically. Next, we estimated relative vascularization changes via T2 mapping with magnetic resonance imaging (MRI) before and after islet transplantation. On the first day post-transplantation, we measured a slight decrease in T2 values followed by a significant increase by day 14 attributable to islet revascularization. Our findings underscore the potential of non-invasive imaging techniques to provide insightful information on the readiness of the transplant site within cell encapsulation systems to support cell graft transplantation.

Keywords

cell encapsulation, computed tomography, contrast‐enhanced imaging, islet transplantation, magnetic resonance imaging, revascularization, T2‐mapping

Published Open-Access

yes

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