Nabil Ahmed, Uto Koichiro, Zahran Faten, Soliman Reham, Hassan Ayman A, Elshemy Mohamed M, Ali Islam S, Ebara Mitsuhiro, Shiha Gamal
Research Center for Functional Materials, National Institute for Materials Science (NIMS), 1-1Namiki, Tsukuba, Ibaraki 305-0044, Japan.
Biotechnology and Life Sciences Department, Faculty of Postgraduate Studies for Advanced Sciences (PSAS), Beni-Suef University, Beni-Suef, Egypt.
Biomed Res Int. 2021 Mar 28;2021:6678913. doi: 10.1155/2021/6678913. eCollection 2021.
Hepatic fibrosis is a progressive disease with serious clinical complications that arise from abnormal propagation and activation of multiple inflammatory pathways. Nilotinib is an oral tyrosine kinase inhibitor with antifibrotic activity. Mesenchymal stem cells (MSCs) are blank cells and can differentiate into specific cell types. They have the potential to repair and regenerate cells. MSCs have a special paracrine fashion where they produce special exosomes, microvesicles, and cytokines like IL-6, transforming growth factor-beta (TGF-), and HGF as well as hepatic stellate cell suppressors. This paracrine fashion can decrease collagen deposition, enhance antifibrotic, anti-inflammatory, and angiogenic activity in vitro and in vivo. In our study, the rat's hepatic stellate cells (HSCs) in addition to different normal cell lines were treated with Nilotinib alone and in combination with liver mesenchymal stem cells conditioned medium (LMSCs-CM) for 24 h. Mono and combined therapy antifibrotic and cytotoxicity effects were evaluated using different parameters including -SMA, cytochrome c, P53 expression, collagen deposition, DNA content, oxidative stress parameters, cell viability, and apoptosis by flow cytometry analysis. Our results showed that Nilotinib and LMSCs-CM in combination had a significantly potent antifibrotic and anti-inflammatory effect on activated hepatic stellate cells than Nilotinib alone; otherwise, this combination showed the best safety with minimal cytotoxicity on different normal cell lines.
肝纤维化是一种进展性疾病,会引发严重的临床并发症,这些并发症源于多种炎症途径的异常传播和激活。尼洛替尼是一种具有抗纤维化活性的口服酪氨酸激酶抑制剂。间充质干细胞(MSCs)是空白细胞,能够分化为特定的细胞类型。它们具有修复和再生细胞的潜力。MSCs具有一种特殊的旁分泌方式,在此过程中它们会产生特殊的外泌体、微泡以及诸如白细胞介素-6、转化生长因子-β(TGF-β)、肝细胞生长因子(HGF)等细胞因子,还有肝星状细胞抑制剂。这种旁分泌方式能够在体外和体内减少胶原蛋白沉积,增强抗纤维化、抗炎和血管生成活性。在我们的研究中,大鼠的肝星状细胞(HSCs)以及不同的正常细胞系分别单独用尼洛替尼处理,并与肝间充质干细胞条件培养基(LMSCs-CM)联合处理24小时。通过流式细胞术分析,使用包括α-平滑肌肌动蛋白(α-SMA)、细胞色素c、P53表达、胶原蛋白沉积、DNA含量、氧化应激参数、细胞活力和凋亡等不同参数评估单一疗法和联合疗法的抗纤维化及细胞毒性作用。我们的结果表明,与单独使用尼洛替尼相比,尼洛替尼与LMSCs-CM联合使用对活化的肝星状细胞具有显著更强的抗纤维化和抗炎作用;此外,这种联合疗法在不同正常细胞系上显示出最佳的安全性,细胞毒性最小。