Rajamani Karthyayani, Lin Yi-Chun, Wen Tung-Chou, Hsieh Jeanne, Subeq Yi-Maun, Liu Jen-Wei, Lin Po-Cheng, Harn Horng-Jyh, Lin Shinn-Zong, Chiou Tzyy-Wen
Department of Life Science and Graduate Institute of Biotechnology, National Dong Hwa University, Hualien, Taiwan.
Cell Transplant. 2015;24(3):493-507. doi: 10.3727/096368915X686959. Epub 2015 Feb 4.
As assuring cell quality is an essential parameter for the success of stem cell therapy, the impact of various senescence-inducing stress signals, and strategies to circumvent them, has been an important area of focus in stem cell research. The aim of this study was to demonstrate the capacity of Trans-cinnamaldehyde (TC) in reversing stress-induced senescence and maintaining the quality of stem cells in a chemically (H2O2)-induced cell senescence model. Because of the availability and the promising application potential in regenerative medicine, adipose-derived stem cells (ADSCs) were chosen for the study. We found that H2O2 treatment resulted in the expression of senescence characteristics in the ADSCs, including decreased proliferation rate, increased senescence-associated β-galactosidase (SA-β-gal) activity, decreased silent mating type information regulation 2 homolog (SIRT1) expression, and decreased telomerase activity. However, TC treatment was sufficient to rescue or reduce the effects of H2O2 induction, ultimately leading to an increased proliferation rate, a decrease in the percentage of SA-β-gal-positive cells, upregulation of SIRT1 expression, and increased telomerase activity of the senescent ADSCs at the cellular level. Moreover, a chemically induced liver fibrosis animal model was used to evaluate the functionality of these rescued cells in vivo. Liver dysfunction was established by injecting 200 mg/kg thioacetamide (TAA) intraperitoneally into Wistar rats every third day for 60 days. The experimental rats were separated into groups: normal group (rats without TAA induction), sham group (without ADSC transplantation), positive control group (transplanted with normal ADSCs), H2O2 group (transplanted with H2O2-induced senescent ADSCs), and H2O2 + TC group (transplanted with ADSCs pretreated with H2O2 and then further treated with TC). In the transplantation group, 1 × 10(6) human ADSCs were introduced into each rat via direct liver injection. Based on the biochemical analysis and immunohistochemical staining results, it was determined that the therapeutic effects on liver fibrosis by the induced senescent ADSCs (H2O2 group) were not as significant as those exerted by the normal ADSCs (the positive control group). However, the H2O2 + TC group showed significant reversal of liver damage when compared to the H2O2 group 1 week posttransplantation. These data confirmed that the TC treatment had the potential to reduce the effects of H2O2-induced senescence and to restore in vivo functionality of the induced senescent ADSCs. It is therefore suggested that TC has potential applications in maintaining the quality of stem cells and could aid in treating senescence-related disorders.
由于确保细胞质量是干细胞治疗成功的关键参数,各种诱导衰老的应激信号的影响以及规避这些信号的策略,一直是干细胞研究的重要关注领域。本研究的目的是在化学(H2O2)诱导的细胞衰老模型中,证明反式肉桂醛(TC)逆转应激诱导的衰老并维持干细胞质量的能力。鉴于其可得性以及在再生医学中颇具前景的应用潜力,本研究选用了脂肪来源干细胞(ADSCs)。我们发现,H2O2处理导致ADSCs出现衰老特征,包括增殖率降低、衰老相关β-半乳糖苷酶(SA-β-gal)活性增加、沉默信息调节因子2同源物(SIRT1)表达降低以及端粒酶活性降低。然而,TC处理足以挽救或减轻H2O2诱导的影响,最终在细胞水平上导致衰老ADSCs的增殖率增加、SA-β-gal阳性细胞百分比降低、SIRT1表达上调以及端粒酶活性增加。此外,使用化学诱导的肝纤维化动物模型来评估这些挽救的细胞在体内的功能。通过每三天向Wistar大鼠腹腔注射200 mg/kg硫代乙酰胺(TAA),持续60天来建立肝功能障碍。将实验大鼠分为以下几组:正常组(未用TAA诱导的大鼠)、假手术组(未进行ADSC移植)、阳性对照组(移植正常ADSCs)、H2O2组(移植H2O2诱导的衰老ADSCs)和H2O2 + TC组(移植先用H2O2预处理然后再用TC进一步处理的ADSCs)。在移植组中,通过直接肝内注射将1×10(6)个人类ADSCs引入每只大鼠体内。根据生化分析和免疫组织化学染色结果,确定诱导衰老的ADSCs(H2O2组)对肝纤维化的治疗效果不如正常ADSCs(阳性对照组)显著。然而,与H2O2组相比,移植后1周H2O2 + TC组显示出肝损伤的显著逆转。这些数据证实,TC处理具有减轻H2O2诱导的衰老影响并恢复诱导衰老的ADSCs体内功能的潜力。因此,提示TC在维持干细胞质量方面具有潜在应用价值,并可能有助于治疗衰老相关疾病。