1. Academic Validation
  2. Long-term in vitro human pancreatic islet culture using three-dimensional microfabricated scaffolds

Long-term in vitro human pancreatic islet culture using three-dimensional microfabricated scaffolds

  • Biomaterials. 2011 Feb;32(6):1536-42. doi: 10.1016/j.biomaterials.2010.10.036.
Jamal T Daoud 1 Maria S Petropavlovskaia Jason M Patapas Christian E Degrandpré Robert W Diraddo Lawrence Rosenberg Maryam Tabrizian
Affiliations

Affiliation

  • 1 Department of Biomedical Engineering, Faculty of Medicine, McGill University, 3775 University Street, Montreal (QC), Canada. jamal.daoud@mail.mcgill.ca
Abstract

Human pancreatic islet in vitro culture is very challenging and requires the presence of various extra cellular matrix (ECM) components in a three-dimensional environment, which provides mechanical and biological support. The development of such an environment is vital in providing favourable conditions to preserve human islets in long-term culture. In this study, we investigated the effects of human islet culture within various three-dimensional environments; collagen I gel, collagen I gel supplemented with ECM components fibronectin and collagen IV, and microfabricated scaffold with ECM-supplemented gel. The cultured human islets were analyzed for functionality, gene expression and hormone content following long-term in vitro culture. It was clear the incorporation of ECM components within the three-dimensional support improved prolonged culture. However, long-term and highly uniform human islet culture within a microfabricated scaffold, with controlled pore structures, coupled with the presence of ECM components, displayed an Insulin release profile similar to freshly isolated islets, yielding a stimulation index of approximately 1.8. Moreover, gene expression was markedly increased for all pancreatic genes, giving a approximately 50-fold elevation of Insulin gene expression with respect to suspension culture. The distribution and presence of pancreatic Hormones was also highly elevated. These findings provide a platform for the long-term maintenance and preservation of human pancreatic islets in vitro.

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