Khosravi-Farsani Somayeh, Zaminy Arash, Kazemi Sedigheh, Hashemzadeh-Chaleshtori Morteza
Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Department of Anatomical Sciences, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Iran J Basic Med Sci. 2022 Jul;25(7):799-807. doi: 10.22038/IJBMS.2022.62642.13860.
The mechanisms underlying the beneficial effects of MSCs on hepatic I/R injury are still poorly described, especially the changes in hepatocyte gene expression. In this study, the effect of bone marrow-derived mesenchymal stem cells (BMSCs) and adipose tissue-derived mesenchymal stem cells (AMSCs) and their conditioned medium on hepatocyte gene expression resulted by I/R shock were investigated.
Liver ischemia models were induced by clamping in experimental groups. Experimental groups received MSCs or conditioned medium treatments and the control group received Dulbecco's Modified Eagle Medium (DMEM). During 1, 24 hr, and 1 week after treatment, the serum levels of alanine aminotransferase (ALT), aspartate transaminase (AST) and lactate dehydrogenase (LDH) enzymes and tissue catalase activity (CAT) were measured. Gene expression of a number of hepatocyte-specific genes (Alb, Afp, and Ck8) and Icam-1 which is upregulated under inflammatory conditions were also evaluated in 5, 24 hr, and 1-week intervals after I/R insult.
In this study, liver enzymes showed a much more shift in the control group than treated groups and it was more noticeable 5 hr post-treatment. Moreover, gene expression pattern of the control group underwent changes after I/R injury. However, treated groups gene expression analysis met a steady trend after I/R insult.
Our finding shows that stem cell treatment has better curative effects than conditioned medium. BMSCs, AMSCs or BMSC and AMSC-derived bioactive molecules injection have potential to be considered as a therapeutic approach for treating acute liver injury.
间充质干细胞(MSCs)对肝缺血/再灌注损伤(I/R损伤)产生有益作用的潜在机制仍未完全阐明,尤其是肝细胞基因表达的变化。在本研究中,我们调查了骨髓间充质干细胞(BMSCs)、脂肪组织来源的间充质干细胞(AMSCs)及其条件培养基对I/R休克所致肝细胞基因表达的影响。
通过夹闭法在实验组诱导肝缺血模型。实验组接受MSCs或条件培养基处理,对照组接受杜氏改良 Eagle培养基(DMEM)。在处理后1小时、24小时和1周,测量血清中丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)和乳酸脱氢酶(LDH)的水平以及组织过氧化氢酶活性(CAT)。在I/R损伤后5小时、24小时和1周的时间间隔内,还评估了一些肝细胞特异性基因(Alb、Afp和Ck8)以及在炎症条件下上调的细胞间黏附分子1(Icam-1)的基因表达。
在本研究中,对照组肝酶的变化比处理组大得多,且在处理后5小时更明显。此外,对照组的基因表达模式在I/R损伤后发生了变化。然而,处理组的基因表达分析在I/R损伤后呈现稳定趋势。
我们的研究结果表明,干细胞治疗比条件培养基具有更好的疗效。注射BMSCs、AMSCs或BMSC和AMSC来源的生物活性分子有潜力被视为治疗急性肝损伤的一种治疗方法。