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

被引:83
|
作者
Daoud, Jamal T. [1 ]
Petropavlovskaia, Maria S. [2 ]
Patapas, Jason M. [2 ]
Degrandpre, Christian E. [3 ]
DiRaddo, Robert W. [3 ]
Rosenberg, Lawrence [2 ]
Tabrizian, Maryam [1 ,4 ,5 ]
机构
[1] McGill Univ, Dept Biomed Engn, Fac Med, Montreal, PQ H3A 2B4, Canada
[2] McGill Univ, Fac Med, Dept Surg, Montreal, PQ H3A 2B4, Canada
[3] NRC, Inst Ind Mat, Boucherville, PQ, Canada
[4] McGill Univ, Fac Dent, Montreal, PQ H3A 2B4, Canada
[5] McGill Univ, Ctr Biorecognit & Biosensors, Montreal, PQ H3A 2B4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
ECM(extracellular matrix); Microfabricated biodegradable scaffold; Long-term culture of human islets; Islet functionality; EXTRACELLULAR-MATRIX; INSULIN-SECRETION; TRANSPLANTATION; DESIGN; MICROENVIRONMENTS; FABRICATION; REVERSAL; GLUCOSE; GROWTH; CELLS;
D O I
10.1016/j.biomaterials.2010.10.036
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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 similar to 1.8. Moreover, gene expression was markedly increased for all pancreatic genes, giving a similar to 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. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1536 / 1542
页数:7
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