蔺晨雨, 陈文, 马锡慧, 等. 骨髓间充质干细胞对小鼠缺血-再灌注急性肾损伤中IL-10和TNF-α表达的影响[J]. 器官移植, 2021, 12(5): 563-570. DOI: 10.3969/j.issn.1674-7445.2021.05.010
引用本文: 蔺晨雨, 陈文, 马锡慧, 等. 骨髓间充质干细胞对小鼠缺血-再灌注急性肾损伤中IL-10和TNF-α表达的影响[J]. 器官移植, 2021, 12(5): 563-570. DOI: 10.3969/j.issn.1674-7445.2021.05.010
Lin Chenyu, Chen Wen, Ma Xihui, et al. Effect of bone marrow mesenchymal stem cell on the expression of IL-10 and TNF-α in mice with ischemia-reperfusion acute kidney injury[J]. ORGAN TRANSPLANTATION, 2021, 12(5): 563-570. DOI: 10.3969/j.issn.1674-7445.2021.05.010
Citation: Lin Chenyu, Chen Wen, Ma Xihui, et al. Effect of bone marrow mesenchymal stem cell on the expression of IL-10 and TNF-α in mice with ischemia-reperfusion acute kidney injury[J]. ORGAN TRANSPLANTATION, 2021, 12(5): 563-570. DOI: 10.3969/j.issn.1674-7445.2021.05.010

骨髓间充质干细胞对小鼠缺血-再灌注急性肾损伤中IL-10和TNF-α表达的影响

Effect of bone marrow mesenchymal stem cell on the expression of IL-10 and TNF-α in mice with ischemia-reperfusion acute kidney injury

  • 摘要:
      目的  探讨骨髓间充质干细胞(BMSC)对小鼠缺血-再灌注急性肾损伤(IR-AKI)过程中白细胞介素(IL)-10和肿瘤坏死因子(TNF)-α表达的影响。
      方法  将小鼠随机分为假手术组(对照组)、缺血-再灌注损伤组(IRI组)和BMSC治疗组(BMSC组),每组6只。检测各组小鼠肾功能及病理学改变;检测各组小鼠肾组织细胞凋亡情况;检测各组小鼠血清IL-10和TNF-α的表达水平。将小鼠BMSC随机分为对照组和缺氧复氧组(IRI组),检测各组细胞上清IL-10和TNF-α的表达水平。
      结果  对照组小鼠肾组织结构正常,IRI组肾组织结构损伤严重,BMSC组损伤较轻。与对照组比较,IRI组和BMSC组肾组织损伤评分较高;与IRI组比较,BMSC组小鼠肾组织损伤学评分较低(均为P < 0.05)。与对照组比较,IRI组小鼠血清肌酐(Scr)和血尿素氮(BUN)水平升高,BMSC组BUN水平升高;与IRI组比较,BMSC组小鼠Scr和BUN水平下降(均为P < 0.05)。IRI组肾组织凋亡细胞数量多于BMSC组和对照组,BMSC组凋亡细胞数量多于对照组(均为P < 0.05)。与对照组比较,IRI组小鼠血清IL-10和TNF-α水平均升高,BMSC组小鼠血清TNF-α水平下降,IL-10水平升高;与IRI组比较,BMSC组小鼠血清IL-10和TNF-α水平均下降(均为P < 0.05)。IRI组细胞上清IL-10、TNF-α水平与对照组比较,差异均无统计学意义(P=0.080、0.627)。
      结论  BMSC输注可降低肾IRI及炎症反应,其机制可能是通过抑制TNF-α表达,而非促进IL-10的表达。

     

    Abstract:
      Objective  To evaluate the effect of bone marrow mesenchymal stem cell (BMSC) on the expression of interleukin (IL)-10 and tumor necrosis factor (TNF)-α in mice with ischemia-reperfusion acute kidney injury (IR-AKI).
      Methods  All mice were randomly divided into the sham operation group (control group), ischemia-reperfusion injury group (IRI group) and BMSC treatment group (BMSC group), with 6 mice in each group, respectively. The renal function and pathological changes of mice were detected. The cell apoptosis of renal tissues of mice was determined. The expression levels of serum IL-10 and TNF-α of mice were quantitatively measured. The mouse BMSC was randomly divided into the control and hypoxia-reoxygenation groups (IRI group), and the expression levels of IL-10 and TNF-α in cell supernatant were determined.
      Results  The renal structure of mice was normal in the control group, severe damage was observed in the IRI group, and mild damage occurred in the BMSC group. Compared with the control group, the renal tissue injury scores were significantly higher in the IRI and BMSC groups (both P < 0.05). Compared with the IRI group, the renal tissue injury score was significantly lower in the BMSC group (P < 0.05). Compared with the control group, the levels of serum creatinine (Scr) and blood urea nitrogen (BUN) were remarkably up-regulated in the IRI group, and the level of BUN was significantly up-regulated in the BMSC group (all P < 0.05). Compared with the IRI group, the levels of Scr and BUN were significantly down-regulated in the BMSC group (both P < 0.05). In the IRI group, the quantity of apoptotic cells in the renal tissues was considerably higher than those in the BMSC and control groups, and the quantity of apoptotic cells in the BMSC group was significantly higher than that in the control group (all P < 0.05). Compared with the control group, the levels of serum IL-10 and TNF-α were significantly up-regulated in the IRI group, whereas the level of serum TNF-α was significantly down-regulated and the level of serum IL-10 was significantly up-regulated in the BMSC group (all P < 0.05). Compared with the IRI group, the levels of serum IL-10 and TNF-α were significantly down-regulated in the BMSC group (both P < 0.05). The levels of IL-10 and TNF-α in the cell supernatant did not significantly differ between the IRI and control groups (P=0.080、0.627).
      Conclusions  BMSC infusion may reduce the incidence of renal IRI and inflammation, probably via the mechanism of down-regulating TNF-α expression rather than up-regulating IL-10 expression.

     

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