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本文引用的文献

1
Organoids as an in vitro model of human development and disease.类器官作为人类发育和疾病的体外模型。
Nat Cell Biol. 2016 Mar;18(3):246-54. doi: 10.1038/ncb3312.
2
Short-range growth inhibitory signals from the epithelium can drive non-stereotypic branching in the pancreas.来自上皮细胞的短程生长抑制信号可驱动胰腺中的非定型分支。
Phys Biol. 2016 Feb 23;13(1):016007. doi: 10.1088/1478-3975/13/1/016007.
3
Co-culture with intestinal epithelial organoids allows efficient expansion and motility analysis of intraepithelial lymphocytes.与肠道上皮类器官共培养可实现上皮内淋巴细胞的高效扩增和运动性分析。
J Gastroenterol. 2016 Mar;51(3):206-13. doi: 10.1007/s00535-016-1170-8. Epub 2016 Jan 22.
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Ductal pancreatic cancer modeling and drug screening using human pluripotent stem cell- and patient-derived tumor organoids.利用人类多能干细胞和患者来源的肿瘤类器官进行胰腺导管癌建模和药物筛选。
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5
Kidney organoids from human iPS cells contain multiple lineages and model human nephrogenesis.人诱导多能干细胞来源的肾类器官包含多种细胞谱系,并可模拟人类肾发生。
Nature. 2015 Oct 22;526(7574):564-8. doi: 10.1038/nature15695. Epub 2015 Oct 7.
6
Cholangiocytes derived from human induced pluripotent stem cells for disease modeling and drug validation.源自人类诱导多能干细胞的胆管细胞用于疾病建模和药物验证。
Nat Biotechnol. 2015 Aug;33(8):845-852. doi: 10.1038/nbt.3275. Epub 2015 Jul 13.
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Prospective derivation of a living organoid biobank of colorectal cancer patients.前瞻性建立结直肠癌患者活体类器官生物样本库。
Cell. 2015 May 7;161(4):933-45. doi: 10.1016/j.cell.2015.03.053.
8
Ex Vivo Expansion and Differentiation of Human and Mouse Fetal Pancreatic Progenitors Are Modulated by Epidermal Growth Factor.人及小鼠胎儿胰腺祖细胞的体外扩增与分化受表皮生长因子调控。
Stem Cells Dev. 2015 Aug 1;24(15):1766-78. doi: 10.1089/scd.2014.0550. Epub 2015 Jun 8.
9
Efficient generation of NKX6-1+ pancreatic progenitors from multiple human pluripotent stem cell lines.从多种人类多能干细胞系高效生成 NKX6-1+ 胰腺祖细胞。
Stem Cell Reports. 2015 Apr 14;4(4):591-604. doi: 10.1016/j.stemcr.2015.02.017. Epub 2015 Apr 2.
10
In vitro generation of human pluripotent stem cell derived lung organoids.人多能干细胞来源的肺类器官的体外生成。
Elife. 2015 Mar 24;4:e05098. doi: 10.7554/eLife.05098.

三维胰腺器官发生模型。

Three-dimensional pancreas organogenesis models.

作者信息

Grapin-Botton A

机构信息

DanStem, University of Copenhagen, Copenhagen, Denmark.

出版信息

Diabetes Obes Metab. 2016 Sep;18 Suppl 1(Suppl 1):33-40. doi: 10.1111/dom.12720.

DOI:10.1111/dom.12720
PMID:27615129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5021194/
Abstract

A rediscovery of three-dimensional culture has led to the development of organ biogenesis, homeostasis and disease models applicable to human tissues. The so-called organoids that have recently flourished serve as valuable models bridging between cell lines or primary cells grown on the bottom of culture plates and experiments performed in vivo. Though not recapitulating all aspects of organ physiology, the miniature organs generated in a dish are useful models emerging for the pancreas, starting from embryonic progenitors, adult cells, tumour cells and stem cells. This review focusses on the currently available systems and their relevance to the study of the pancreas, of β-cells and of several pancreatic diseases including diabetes. We discuss the expected future developments for studying human pancreas development and function, for developing diabetes models and for producing therapeutic cells.

摘要

三维培养的重新发现推动了适用于人体组织的器官生物发生、内稳态及疾病模型的发展。最近蓬勃发展的所谓类器官,是连接培养皿底部生长的细胞系或原代细胞与体内实验的宝贵模型。尽管不能概括器官生理学的所有方面,但在培养皿中生成的微型器官是从胚胎祖细胞、成体细胞、肿瘤细胞和干细胞开始,为胰腺研究出现的有用模型。本综述聚焦于当前可用的系统及其与胰腺、β细胞以及包括糖尿病在内的几种胰腺疾病研究的相关性。我们讨论了研究人类胰腺发育和功能、开发糖尿病模型以及生产治疗性细胞的预期未来发展。