Wang Wei, Liu Xueyong, Wang Wei, Li Jinghua, Li Yuanyuan, Li Liping, Wang Shaohua, Zhang Jianchun, Zhang Youkang, Huang Haichang
The Kidney Disease Research Center, Jingdong Yumei Kidney Disease Hospital, Beijing, China.
Cell Physiol Biochem. 2016;38(1):401-14. doi: 10.1159/000438639. Epub 2016 Jan 29.
BACKGROUND/AIMS: Indoxyl sulfate, an important protein-bound uremic toxin, can damage stem cells, thus hampering stem cell-based regenerative medicine approaches targeting chronic kidney diseases (CKD). Human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) are thought to have promising clinical application because of their high proliferative potential and ease of isolation than MSCs from other sources. In the present study, we aimed to determine the harmful effects of indoxyl sulfate on the phenotype and functional potential of hUC-MSCs in vitro.
The toxicity and cell viability was examined by Trypan blue exclusion and MTT assay. The cellular surface markers and the percentage of apoptotic cells by Annexin-V/PI staining were analyzed by flow cytometry. Proliferation was evaluated based on cell number counting and Ki-67 immunostaining. Cell senescence was measured using senescence-associated β-Galactosidase activity. The ability to stimulate the development of CD4+CD25+FoxP3+ regulatory T cells was assessed by incubating hUC-MSCs with peripheral blood mononuclear cells from the healthy volunteers.
Our results demonstrated that the immunophenotype of hUC-MSCs was not affected by indoxyl sulfate flow cytometry. However, a significant decrease in cell numbers and fraction of Ki-67 positive proliferating cells, along with a significant increase in cellular senescence were detected in hUC-MSCs after exposure to indoxyl sulfate. Additionally, their ability to stimulate CD4+CD25+FoxP3+ regulatory T cell production was compromised when hUC-MSCs were pretreated with indoxyl sulfate.
Taken together, our study clearly demonstrated that the molecular alterations and functional incompetence in hUC-MSCs under the challenge of indoxyl sulfate in vitro.
背景/目的:硫酸吲哚酚是一种重要的蛋白结合尿毒症毒素,可损伤干细胞,从而阻碍针对慢性肾脏病(CKD)的基于干细胞的再生医学方法。人脐带间充质干细胞(hUC-MSCs)因其高增殖潜能且比其他来源的间充质干细胞易于分离,被认为具有广阔的临床应用前景。在本研究中,我们旨在确定硫酸吲哚酚对体外hUC-MSCs表型和功能潜能的有害影响。
通过台盼蓝排斥试验和MTT法检测毒性和细胞活力。采用流式细胞术分析细胞表面标志物以及Annexin-V/PI染色法检测凋亡细胞百分比。基于细胞计数和Ki-67免疫染色评估增殖情况。使用衰老相关β-半乳糖苷酶活性检测细胞衰老。通过将hUC-MSCs与健康志愿者的外周血单个核细胞共培养,评估其刺激CD4+CD25+FoxP3+调节性T细胞发育的能力。
我们的结果表明,硫酸吲哚酚流式细胞术未影响hUC-MSCs的免疫表型。然而,暴露于硫酸吲哚酚后,hUC-MSCs中细胞数量和Ki-67阳性增殖细胞比例显著降低,同时细胞衰老显著增加。此外,当hUC-MSCs用硫酸吲哚酚预处理时,其刺激CD4+CD25+FoxP3+调节性T细胞产生的能力受损。
综上所述,我们的研究清楚地表明了体外硫酸吲哚酚挑战下hUC-MSCs的分子改变和功能缺陷。