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糖尿病的细胞替代与再生疗法。

Cell replacement and regeneration therapy for diabetes.

作者信息

Jun Hee-Sook

机构信息

Lee Gil Ya Cancer and Diabetes Institute, Gachon University of Medicine and Science, Incheon, Korea.

出版信息

Korean Diabetes J. 2010 Apr;34(2):77-83. doi: 10.4093/kdj.2010.34.2.77. Epub 2010 Apr 30.

DOI:10.4093/kdj.2010.34.2.77
PMID:20548838
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2883354/
Abstract

Reduction of beta cell function and a beta cell mass is observed in both type 1 and type 2 diabetes. Therefore, restoration of this deficiency might be a therapeutic option for treatment of diabetes. Islet transplantation has benefits, such as reduced incidence of hypoglycemia and achievement of insulin independence. However, the major drawback is an insufficient supply of islet donors. Transplantation of cells differentiated in vitro or in vivo regeneration of insulin-producing cells are possible approaches for beta cell/islet regenerative therapy. Embryonic and adult stem cells, pancreatic ductal progenitor cells, acinar cells, and other endocrine cells have been shown to differentiate into pancreatic beta cells. Formation of fully functional beta cells and the safety of these cells are critical issues for successful clinical application.

摘要

在1型和2型糖尿病中均观察到β细胞功能和β细胞数量的减少。因此,恢复这种缺陷可能是糖尿病治疗的一种选择。胰岛移植有诸多益处,如低血糖发生率降低以及实现胰岛素非依赖。然而,主要缺点是胰岛供体供应不足。体外分化细胞的移植或体内胰岛素产生细胞的再生是β细胞/胰岛再生治疗的可行方法。胚胎干细胞、成体干细胞、胰腺导管祖细胞、腺泡细胞和其他内分泌细胞已被证明可分化为胰腺β细胞。形成功能完全的β细胞以及这些细胞的安全性是成功临床应用的关键问题。

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Cell replacement and regeneration therapy for diabetes.糖尿病的细胞替代与再生疗法。
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Meeting the need for regenerative therapies I: target-based incidence and its relationship to U.S. spending, productivity, and innovation.满足再生疗法的需求 I:基于目标的发病率及其与美国支出、生产力和创新的关系。
Tissue Eng Part B Rev. 2012 Apr;18(2):139-54. doi: 10.1089/ten.TEB.2011.0454. Epub 2012 Jan 16.

本文引用的文献

1
Adult stem cells as a renewable source of insulin-producing cells.成体干细胞作为胰岛素产生细胞的可再生来源。
Int J Stem Cells. 2009 May;2(2):115-21. doi: 10.15283/ijsc.2009.2.2.115.
2
In vivo regeneration of insulin-producing beta-cells.体内胰岛素分泌β细胞的再生。
Adv Exp Med Biol. 2010;654:627-40. doi: 10.1007/978-90-481-3271-3_27.
3
Insulin expressed from endogenously active glucose-responsive EGR1 promoter in bone marrow mesenchymal stromal cells as diabetes therapy.骨髓间充质基质细胞中内源性活性葡萄糖反应 EGR1 启动子表达的胰岛素作为糖尿病治疗。
Gene Ther. 2010 May;17(5):592-605. doi: 10.1038/gt.2010.12. Epub 2010 Feb 25.
4
Amelioration of hyperglycemia by intestinal overexpression of glucagon-like peptide-1 in mice.肠道过表达胰高血糖素样肽-1可改善小鼠的高血糖。
J Mol Med (Berl). 2010 Apr;88(4):351-8. doi: 10.1007/s00109-009-0571-z. Epub 2009 Dec 17.
5
Prospects and challenges for islet regeneration as a treatment for diabetes: a review of islet neogenesis associated protein.胰岛再生作为糖尿病治疗方法的前景与挑战:胰岛新生相关蛋白综述
J Diabetes Sci Technol. 2007 Mar;1(2):231-44. doi: 10.1177/193229680700100214.
6
Insulin-secreting cells from human eyelid-derived stem cells alleviate type I diabetes in immunocompetent mice.人眼睑干细胞来源的胰岛素分泌细胞可缓解免疫活性小鼠的 I 型糖尿病。
Stem Cells. 2009 Aug;27(8):1999-2008. doi: 10.1002/stem.127.
7
Embryonic pig pancreatic tissue for the treatment of diabetes in a nonhuman primate model.用于非人灵长类动物模型中治疗糖尿病的胚胎猪胰腺组织。
Proc Natl Acad Sci U S A. 2009 May 26;106(21):8659-64. doi: 10.1073/pnas.0812253106. Epub 2009 May 11.
8
Neurogenin3 is sufficient for transdetermination of hepatic progenitor cells into neo-islets in vivo but not transdifferentiation of hepatocytes.神经生成素3足以使肝祖细胞在体内转决定为新胰岛,但不能使肝细胞转分化。
Dev Cell. 2009 Mar;16(3):358-73. doi: 10.1016/j.devcel.2009.01.012.
9
Treatment of type 1 diabetes with adipose tissue-derived stem cells expressing pancreatic duodenal homeobox 1.用表达胰腺十二指肠同源盒 1 的脂肪组织源性干细胞治疗 1 型糖尿病。
Stem Cells Dev. 2009 Dec;18(10):1399-406. doi: 10.1089/scd.2009.0010.
10
2008 Update from the Collaborative Islet Transplant Registry.来自协作胰岛移植登记处的2008年更新
Transplantation. 2008 Dec 27;86(12):1783-8. doi: 10.1097/TP.0b013e3181913f6a.