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利用小鼠胚胎肝脏外植体扩增肝干细胞和造血干细胞。

Expansion of hepatic and hematopoietic stem cells utilizing mouse embryonic liver explants.

作者信息

Monga S P, Tang Y, Candotti F, Rashid A, Wildner O, Mishra B, Iqbal S, Mishra L

机构信息

Laboratory of GI Development and Molecular Biology, DVAMC, Washington, DC 20422, USA.

出版信息

Cell Transplant. 2001 Jan-Feb;10(1):81-9.

Abstract

Ex vivo embryonic liver explant culture is a novel and attractive approach to obtain abundant hepatic and hematopoietic stem cells. Gene therapy of autologous hepatic and hematopoietic stem cells represents an alternative therapeutic approach to liver transplantation for genetic and metabolic disorders. In this study we characterize the growth and differentiation of hepatic stem cells utilizing embryonic liver cultures. Day 9.5 liver buds are microdissected and cultured under specific conditions. Modulation of growth conditions by addition of hepatocyte growth factor, Flt-3 ligand, and stem cell factor leads to enrichment of hepatic progenitor cells in embryonic liver explants. Under these conditions, we also demonstrate the role of a novel marker PRAJA-1 to identify hepatic stem cells and transitional hepatocytes. Utilization of dexamethasone enhanced pseudolobule formation with increased hepatocytic and biliary differentiation. Transforming growth factor-beta leads to enrichment of biliary cells in the culture. Gut formation is enhanced in the presence of interleukin-3 and blood formation by increasing the mesodermal tissue in these cultures. We also show increased retroviral-mediated expression of the green fluorescent protein expression in the expanded hepatic and hematopoietic stem cells under different culture conditions. Thus, the embryonic liver explant culture is an attractive source for hepatic progenitors and is a possible step towards generating nontumorigenic immortalized hepatocytes with possible transplantation applications.

摘要

体外胚胎肝外植体培养是一种获取丰富的肝干细胞和造血干细胞的新颖且有吸引力的方法。对自体肝干细胞和造血干细胞进行基因治疗是针对遗传和代谢紊乱的肝移植的一种替代治疗方法。在本研究中,我们利用胚胎肝培养来表征肝干细胞的生长和分化。将第9.5天的肝芽进行显微解剖,并在特定条件下培养。通过添加肝细胞生长因子、Flt-3配体和干细胞因子来调节生长条件,可使胚胎肝外植体中的肝祖细胞富集。在这些条件下,我们还证明了一种新型标志物PRAJA-1在识别肝干细胞和过渡性肝细胞中的作用。地塞米松的使用增强了假小叶的形成,并增加了肝细胞和胆管细胞的分化。转化生长因子-β导致培养物中胆管细胞的富集。在白细胞介素-3存在的情况下,肠道形成增强,并且通过增加这些培养物中的中胚层组织促进血液形成。我们还表明,在不同培养条件下,逆转录病毒介导的绿色荧光蛋白在扩增的肝干细胞和造血干细胞中的表达增加。因此,胚胎肝外植体培养是肝祖细胞的一个有吸引力的来源,并且是朝着生成具有潜在移植应用的无致瘤性永生化肝细胞迈出的可能一步。

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