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MiRNA-375 promotes beta pancreatic differentiation in human induced pluripotent stem (hiPS) cells.微小RNA-375促进人诱导多能干细胞(hiPS细胞)向胰腺β细胞分化。
Mol Biol Rep. 2014;41(4):2055-66. doi: 10.1007/s11033-014-3054-4. Epub 2014 Jan 29.

本文引用的文献

1
Persistent donor cell gene expression among human induced pluripotent stem cells contributes to differences with human embryonic stem cells.人诱导多能干细胞中的持续供体细胞基因表达导致其与人胚胎干细胞存在差异。
PLoS One. 2010 Feb 1;5(2):e8975. doi: 10.1371/journal.pone.0008975.
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Generation of pluripotent stem cells from patients with type 1 diabetes.从1型糖尿病患者中生成多能干细胞。
Proc Natl Acad Sci U S A. 2009 Sep 15;106(37):15768-73. doi: 10.1073/pnas.0906894106. Epub 2009 Aug 31.
3
Induced pluripotent stem cells and embryonic stem cells are distinguished by gene expression signatures.诱导多能干细胞和胚胎干细胞通过基因表达特征来区分。
Cell Stem Cell. 2009 Jul 2;5(1):111-23. doi: 10.1016/j.stem.2009.06.008.
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Generation of induced pluripotent stem cells using recombinant proteins.利用重组蛋白生成诱导多能干细胞。
Cell Stem Cell. 2009 May 8;4(5):381-4. doi: 10.1016/j.stem.2009.04.005. Epub 2009 Apr 23.
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A fresh look at iPS cells.对诱导多能干细胞的全新审视。
Cell. 2009 Apr 3;137(1):13-7. doi: 10.1016/j.cell.2009.03.034.
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Human induced pluripotent stem cells free of vector and transgene sequences.无载体和转基因序列的人诱导多能干细胞
Science. 2009 May 8;324(5928):797-801. doi: 10.1126/science.1172482. Epub 2009 Mar 26.
7
Parkinson's disease patient-derived induced pluripotent stem cells free of viral reprogramming factors.不含病毒重编程因子的帕金森病患者来源诱导多能干细胞
Cell. 2009 Mar 6;136(5):964-77. doi: 10.1016/j.cell.2009.02.013.
8
Highly efficient differentiation of human ES cells and iPS cells into mature pancreatic insulin-producing cells.人类胚胎干细胞和诱导多能干细胞高效分化为成熟的胰腺胰岛素分泌细胞。
Cell Res. 2009 Apr;19(4):429-38. doi: 10.1038/cr.2009.28.
9
piggyBac transposition reprograms fibroblasts to induced pluripotent stem cells.piggyBac转座将成纤维细胞重编程为诱导多能干细胞。
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10
Virus-free induction of pluripotency and subsequent excision of reprogramming factors.无病毒诱导多能性及随后重编程因子的切除
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诱导多能干细胞技术与糖尿病的干细胞治疗

Induced pluripotent stem cell technology and stem cell therapy for diabetes.

作者信息

Drummond Robert J, Kunath Tilo, Mee P Joseph, Ross James A

机构信息

Tissue Injury and Repair Group, MRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, Scotland EH16 4SB;

出版信息

Exp Ther Med. 2011 Jan;2(1):3-7. doi: 10.3892/etm.2010.173. Epub 2010 Dec 2.

DOI:10.3892/etm.2010.173
PMID:22977463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3440679/
Abstract

Although diabetes can be managed clinically with the use of insulin injections, it remains an incurable and inconvenient disorder. In the long-term, it is associated with a number of clinical complications, such as cardiovascular disease, resulting in a desire for the development of new methodologies to replace defective cells and provide a lasting normality without the need for drug treatment. Stem cells, including induced pluripotent stem cells, offer the possibility of generating cells suitable for transplantation due to their capacity to differentiate into all tissue lineages. However, many issues must be addressed before this type of treatment becomes a reality, including the need for a greater understanding of the underlying biology involved in the onset of diabetes.

摘要

尽管糖尿病可以通过注射胰岛素进行临床治疗,但它仍然是一种无法治愈且不便的疾病。从长远来看,它会引发许多临床并发症,如心血管疾病,这使得人们渴望开发新方法来替代有缺陷的细胞,并在无需药物治疗的情况下实现持久的正常状态。干细胞,包括诱导多能干细胞,因其能够分化为所有组织谱系,提供了生成适合移植细胞的可能性。然而,在这种治疗成为现实之前,必须解决许多问题,包括需要更深入地了解糖尿病发病背后的生物学机制。