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Reversal of Diabetes in Rats Using GLP-1-Expressing Adult Pancreatic Duct-Like Precursor Cells Transformed From Acinar to Ductal Cells

机译:使用表达GLP-1的成人胰腺导管样前体细胞从腺泡转化为导管细胞逆转大鼠糖尿病

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摘要

Pancreatic injury induces replacement of exocrine acinar cells with ductal cells. These ductal cells have the potential to regenerate the pancreas, but their origin still remains unknown. It has been reported that adult pancreatic acinar cells have the potential to transdifferentiate to ductal progenitor cells. In this regards, we established novel adult pancreatic duct-like progenitor cell lines YGIC4 and YGIC5 and assessed the usefulness of these ductal progenitors in the cell therapy of diabetic rats. Acinar cells were cultured from pancreata of male Sprague Dawley rats and gradually attained ductal cell characteristics, such as expression of CK19 and CFTR with a concomitant down-regulation of amylase expression over time, suggesting transdifferentiation from acinar to ductal cells. During cell culture, the expression of Pdx-1, c-Kit, and vimentin peaked and then decreased, suggesting that transdifferentiation recapitulated embryogenesis. Overexpression of pancreas development regulatory genes and CK19, as well as the ability to differentiate into insulin-producing cells, suggests that the YGIC5 cells had characteristics of pancreatic progenitor cells. Finally, YGIC5 cells coexpressing Green fluorescent protein (GFP) and glucagon-like peptide (GLP)-1 under the activation of a zinc-inducible metallothionein promoter were intravenously infused to STZ-induced diabetic rats. Hyperglycemia was ameliorated with elevation of plasma insulin, and GFP-positive donor cells were colocalized in the acinar and islet areas of recipient pancreata following zinc treatment. In conclusion, after establishing pancreatic progenitor cell lines YGIC4 and YGIC5 under the concept of acinar to ductal transdifferentiation in vitro, we demonstrate how these adult pancreatic stem/progenitor cells can be used to regulate adult pancreatic differentiation toward developing therapy for pancreatic disease such as diabetes mellitus.
机译:胰腺损伤诱导外分泌腺泡细胞被导管细胞替代。这些导管细胞具有再生胰腺的潜力,但其起源仍然未知。据报道,成年胰腺腺泡细胞具有向导管祖细胞转分化的潜力。在这一方面,我们建立了新型的成年胰腺导管样祖细胞系YGIC4和YGIC5,并评估了这些导管祖细胞在糖尿病大鼠细胞治疗中的实用性。从雄性Sprague Dawley大鼠的胰腺中培养腺泡细胞,逐渐达到导管细胞的特性,例如CK19和CFTR的表达,同时淀粉酶表达随时间的下调,提示从腺泡向导管细胞的转分化。在细胞培养过程中,Pdx-1,c-Kit和波形蛋白的表达达到峰值,然后下降,这表明转分化重现了胚胎发生。胰腺发育调节基因和CK19的过表达,以及分化为产生胰岛素的细胞的能力,表明YGIC5细胞具有胰腺祖细胞的特征。最后,在锌诱导的金属硫蛋白启动子的激活下,将共表达绿色荧光蛋白(GFP)和胰高血糖素样肽(GLP)-1的YGIC5细胞静脉输注到STZ诱导的糖尿病大鼠中。血浆胰岛素升高可改善高血糖症,锌治疗后,GFP阳性供体细胞共定位于受体胰腺的腺泡和胰岛区域。总之,在腺泡到导管的转分化概念下建立了胰腺祖细胞系YGIC4和YGIC5之后,我们证明了这些成年的胰腺干/祖细胞可用于调节成年的胰腺分化,从而发展针对诸如糖尿病等胰腺疾病的疗法的。

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  • 来源
    《Stem Cells and Development》 |2009年第7期|991-1002|共12页
  • 作者单位

    Department of Internal Medicine, Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.|Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea.;

    Department of Internal Medicine, Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.|Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea.;

    Department of Internal Medicine, Inha University College of Medicine, Incheon, Korea.;

    Department of Internal Medicine, Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.;

    Endocrinology and Institute of Endocrine Research, Yonsei University College of Medicine, Seoul, Korea.|Endocrinology, Department of Medicine, Northwestern University, Feinberg School of Medicine, Chicago, Illinois.;

    Department of Internal Medicine, Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.|Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea.;

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