ATSC transplantation contributes to liver regeneration following paracetamol-induced acute liver injury through differentiation into hepatic-like cells.

IF 1.5 Q4 CELL BIOLOGY
American journal of stem cells Pub Date : 2020-06-15 eCollection Date: 2020-01-01
Themistoklis Feretis, Charalampos Katselis, Ioannis G Papanikolaou, Konstantinos Apostolou, Spyridon Tsikalakis, Konstantinos G Toutouzas, George Theodoropoulos, Eleni Andrianna Trigka, Angelica A Saetta, Nicholas Alexakis, Manousos Konstandoulakis, Kalliopi Tsarea, Maria Karamperi, Dimitrios Kletsas, Efstratios Patsouris, Andreas Manouras, Georgios C Zografos, Apostolos Papalois
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Abstract

Introduction: Drug-induced liver injury (DILI) is a leading cause of acute liver injury (ALI). Acetaminophen (also termed paracetamol), can often be found in drugs that may be abused (i.e., prescription for pain relief). Animal experiments have shown that mesenchymal stem cell transplantation can ameliorate or even reverse hepatic injury.

Material and methods: ALI was induced in Wistar rats using paracetamol. ATSCs were transplanted via the intravenous, portal vein, or intrahepatic route directly onto the liver parenchyma. Histological evaluation was conducted to assess drug-induced injury following transplantation. Fluorescence in situ hybridization (FISH) was used to verify the location of stem cells on the liver parenchyma. The effect of those cells on liver regeneration was tested by immunohistochemistry for hepatic growth factor (HGF). In addition, reverse transcription-quantitative PCR (qRT-PCR) was used to assess hepatic growth factor (HGF), hepatic nuclear factor 4α (HNF4α), cytochrome P450 1A2 (CYP1A2) and α-fetoprotein (AFP) mRNA expression.

Results: Immunohistochemical staining for HGF was stronger in the transplanted groups than that in the control group (P<0.001). HNF4α and HGF mRNA levels were increased on day 7 following transplantation (P<0.001 and P=0.009, respectively). CYP1A2 mRNA levels were also increased (P=0.013) in the intravenous groups, while AFP levels were higher in the intrahepatic groups (P=0.006). ATSC transplantation attenuates ALI injury and promotes liver regeneration. Furthermore, expression of specific hepatic enzymes points to ATSC hepatic differentiation.

Conclusion: The study showed the positive effects of transplanted adipose tissue stem cells (ATSCs) on liver regeneration (LG) through hepatotrophic factors. Furthermore, increased expression of hepatic specific proteins was recorded in ATSC transplanted groups that indicate stem cells differentiation into hepatic cells.

通过向肝样细胞的分化,ATSC移植有助于扑热息痛诱导的急性肝损伤后的肝脏再生。
药物性肝损伤(DILI)是急性肝损伤(ALI)的主要原因。对乙酰氨基酚(也称为扑热息痛),通常可以在可能被滥用的药物中找到(即,用于缓解疼痛的处方)。动物实验表明,间充质干细胞移植可以改善甚至逆转肝损伤。材料与方法:对乙酰氨基酚诱导Wistar大鼠ALI。ATSCs通过静脉、门静脉或肝内途径直接移植到肝实质上。对移植后药物性损伤进行组织学评价。采用荧光原位杂交技术(FISH)验证干细胞在肝实质上的位置。采用免疫组化法检测肝生长因子(HGF)对肝再生的影响。此外,采用逆转录定量PCR (qRT-PCR)检测肝生长因子(HGF)、肝核因子4α (HNF4α)、细胞色素P450 1A2 (CYP1A2)和α-胎蛋白(AFP) mRNA的表达。结果:移植组HGF免疫组化染色明显强于对照组(p)。结论:移植脂肪组织干细胞(ATSCs)通过肝营养因子对肝再生(LG)有积极作用。此外,在ATSC移植组中,肝脏特异性蛋白的表达增加,表明干细胞分化为肝细胞。
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