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首页> 外文期刊>American Journal of Transplantation >Successful Transplantation of Reduced-Sized Rat Alcoholic Fatty Livers Made Possible by Mobilization of Host Stem Cells
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Successful Transplantation of Reduced-Sized Rat Alcoholic Fatty Livers Made Possible by Mobilization of Host Stem Cells

机译:通过动员宿主干细胞成功实现尺寸缩小的大鼠酒精性脂肪肝的成功移植

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摘要

Livers from Lewis rats fed with 7% alcohol for 5 weeks were used for transplantation. Reduced sized (50%) livers or whole livers were transplanted into normal DA recipients, which, in this strain combination, survive indefinitely when the donor has not been fed alcohol. However, none of the rats survived a whole fatty liver transplant while six of seven recipients of reduced sized alcoholic liver grafts survived long term. SDF-1 and HGF were significantly increased in reduced size liver grafts compared to whole liver grafts. Lineage-negative Thy-1+CXCR4+CD133+ stem cells were significantly increased in the peripheral blood and in allografts after reduced size fatty liver transplantation. In contrast, there were meager increases in cells reactive with anti Thy-1, CXCR4 and CD133 in peripheral blood and allografts in whole alcoholic liver recipients. The provision of plerixafor, a stem cell mobilizer, salvaged 5 of 10 whole fatty liver grafts. Conversely, blocking SDF-1 activity with neutralizing antibodies diminished stem cell recruitment and four of five reduced sized fatty liver recipients died. Thus chemokine insufficiency was associated with transplant failure of whole grafts, which was overcome by the increased regenerative requirements promoted by the small grafts and mediated by SDF-1 resulting in stem cell influx.
机译:来自Lewis大鼠的肝脏用7%的酒精喂养5周,用于移植。尺寸缩小(50%)的肝脏或全肝被移植到正常的DA受体中,在这种菌株组合中,当供体未喂酒时,它们可以无限期存活。但是,没有大鼠在整个脂肪肝移植中幸存下来,而在七个尺寸缩小的酒精性肝移植受者中,有六个可以长期存活。与全肝移植相比,尺寸缩小的肝移植中SDF-1和HGF显着增加。脂肪肝移植缩小后,外周血和同种异体移植中沿袭阴性的Thy-1 + CXCR4 + CD133 +干细胞显着增加。相反,在全酒精肝受体中,外周血和同种异体移植物中与抗Thy-1,CXCR4和CD133反应的细胞微不足道增加。干细胞动员剂plerixafor的使用挽救了10例全脂肝移植物中的5例。相反,用中和抗体阻断SDF-1活性可减少干细胞募集,五分之四的脂肪肝接受者死亡。因此,趋化因子不足与整个移植物的移植失败有关,这可以通过小移植物促进并由SDF-1介导的导致干细胞大量涌入的再生需求增加来克服。

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