Taléns-Visconti Raquel, Bonora Ana, Jover Ramiro, Mirabet Vicente, Carbonell Francisco, Castell José-Vicente, Gómez-Lechón María José
Unidad de Hepatologia Experimental, Centro de Investigacion. Hospital Universitario La Fe, Avda Campanar 21, E-46009-Valencia, Spain.
World J Gastroenterol. 2006 Sep 28;12(36):5834-45. doi: 10.3748/wjg.v12.i36.5834.
To investigate and compare the hepatogenic transdifferentiation of adipose tissue-derived stem cells (ADSC) and bone marrow-derived mesenchymal stem cells (BMSC) in vitro. Transdifferentiation of BMSC into hepatic cells in vivo has been described. Adipose tissue represents an accessible source of ADSC, with similar characteristics to BMSC.
BMSCs were obtained from patients undergoing total hip arthroplasty and ADSC from human adipose tissue obtained from lipectomy. Cells were grown in medium containing 15% human serum. Cultures were serum deprived for 2 d before cultivating under similar pro-hepatogenic conditions to those of liver development using a 2-step protocol with sequential addition of growth factors, cytokines and hormones. Hepatic differentiation was RT-PCR-assessed and liver-marker genes were immunohistochemically analysed.
BMSC and ADSC exhibited a fibroblastic morphology that changed to a polygonal shape when cells differentiated. Expression of stem cell marker Thy1 decreased in differentiated ADSC and BMSC. However, the expression of the hepatic markers, albumin and CYPs increased to a similar extent in differentiated BMSC and ADSC. Hepatic gene activation could be attributed to increased liver-enriched transcription factors (C/EBPbeta and HNF4alpha), as demonstrated by adenoviral expression vectors.
Mesenchymal stem cells can be induced to hepatogenic transdifferentiation in vitro. ADSCs have a similar hepatogenic differentiation potential to BMSC, but a longer culture period and higher proliferation capacity. Therefore, adipose tissue may be an ideal source of large amounts of autologous stem cells, and may become an alternative for hepatocyte regeneration, liver cell transplantation or preclinical drug testing.
在体外研究并比较脂肪组织来源干细胞(ADSC)和骨髓间充质干细胞(BMSC)向肝细胞的转分化。已报道BMSC在体内可向肝细胞转分化。脂肪组织是ADSC的一个可获取来源,其与BMSC具有相似特征。
BMSC取自接受全髋关节置换术的患者,ADSC取自抽脂获得的人体脂肪组织。细胞在含15%人血清的培养基中培养。在使用两步方案依次添加生长因子、细胞因子和激素,在与肝脏发育相似的促肝细胞生成条件下培养前,将培养物血清饥饿2天。通过RT-PCR评估肝细胞分化情况,并对肝脏标志物基因进行免疫组织化学分析。
BMSC和ADSC呈现成纤维细胞形态,在分化时变为多边形。干细胞标志物Thy1在分化的ADSC和BMSC中的表达降低。然而,肝脏标志物白蛋白和细胞色素P450(CYPs)在分化的BMSC和ADSC中的表达增加程度相似。腺病毒表达载体证明,肝脏基因激活可归因于肝脏富集转录因子(C/EBPβ和HNF4α)增加。
间充质干细胞在体外可被诱导向肝细胞转分化。ADSC与BMSC具有相似的肝细胞分化潜能,但培养期更长且增殖能力更高。因此,脂肪组织可能是大量自体干细胞的理想来源,并可能成为肝细胞再生、肝细胞移植或临床前药物测试的替代物。