The in vitro differentiation of rat neural stem cells into an insulin-expressing phenotype

被引:14
作者
Burns, CJ [1 ]
Minger, SL
Hall, S
Milne, H
Ramracheya, RD
Evans, ND
Persaud, SJ
Jones, PM
机构
[1] Kings Coll London, Beta Cell Dev & Funct Grp, London SE1 1UL, England
[2] Kings Coll London, Wolfson Ctr Agerelated Dis, London SE1 1UL, England
基金
英国工程与自然科学研究理事会;
关键词
neural stem cell; pancreatic beta-cell; insulin gene; signal recognition; islet transplantation; diabetes mellitus;
D O I
10.1016/j.bbrc.2004.11.062
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mature beta-cells and nerve cells share many functional similarities despite originating from different embryonic germ layers. The aim of this study was to investigate the potential of neural stem cells (NSCs), isolated from foetal rat brain, as a starting material from which to generate functionally responsive, insulin-containing cells. Our results demonstrated that NSCs can be significantly expanded in vitro and can be induced to express increased preproinsulin mRNA levels. In addition, these NSC-derived cells expressed transcriptional and functional elements associated with a mature beta-cell phenotype. The differentiated cells showed functional responses typical of pancreatic beta-cells, including glucose-dependent increases in metabolism and rapid elevations in intracellular Ca2+ in response to the sulphonylurea tolbutamide or to increased glucose concentration. These results suggest that NSCs may have potential as a starting material from which to generate beta-cell surrogates for the treatment of patients with Type 1 diabetes mellitus. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:570 / 577
页数:8
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