首页> 美国卫生研究院文献>International Journal of Immunopathology and Pharmacology >Effects of total flavonoids of sea buckthorn (Hippophae rhamnoides L.) on cytotoxicity of NK92-MI cells
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Effects of total flavonoids of sea buckthorn (Hippophae rhamnoides L.) on cytotoxicity of NK92-MI cells

机译:沙棘总黄酮对NK92-MI细胞杀伤作用的影响

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摘要

Sea buckthorn (Hippophae rhamnoides L.) has multifarious medicinal properties including immunoregulatory effect. The total flavonoids of Hippophae rhamnoides L. (TFH) are the main active components isolated from berries of sea buckthorn. The aim of this study was to evaluate the effects of TFH on the cytotoxicity of NK92-MI cells and its possible mechanisms. NK92-MI cells were treated with TFH (2.5 or 5.0 mg/L) or phosphate-buffered saline (PBS) for 24 h, the cytotoxicity against K562 was detected by measuring the release of lactate dehydrogenase (LDH), expression levels of NCRs (NKp30, NKp44, NKp46) and NKG2D were detected by flow cytometry, and expression levels of perforin and granzyme B were detected by western blot. Cytokine Antibody Arrays with 80 cytokine proteins were used to profile the effect of TFH on cytokines. Western blot was adopted to detect the effects of TFH on STAT1, STAT4, and STAT5 signal pathway. Compared with the normal control group, TFH could significantly enhance NK92-MI cell cytotoxicity against K562 cells, upregulate expressions of NKp44, NKp46, perforin, and granzyme B. TFH could upregulate expressions of IL-1α, IL-2, IL-7, IL-15, CSF-2, CSF-3, MCP-1, MIG, IFN-γ, TNF-α, and TNF-β and downregulate expressions of IL-16, MIP-1β, CX3CL-1, and MIF. TFH could increase expressions of phospho-STAT1 and phospho-STAT5. The results suggest that TFH stimulated NK92-MI cells to activate and enhance cytotoxicity of NK92-MI cells.
机译:沙棘(Hippophae rhamnoides L.)具有多种医学特性,包括免疫调节作用。沙棘(TFH)的总黄酮是从沙棘浆果中分离出来的主要活性成分。这项研究的目的是评估TFH对NK92-MI细胞的细胞毒性的影响及其可能的机制。用TFH(2.5或5.0 mg / L)或磷酸盐缓冲盐水(PBS)处理NK92-MI细胞24小时,通过测量乳酸脱氢酶(LDH)的释放,NCRs的表达水平来检测针对K562的细胞毒性流式细胞仪检测NKp30,NKp44,NKp46)和NKG2D,Western blot检测穿孔素和颗粒酶B的表达水平。使用具有80种细胞因子蛋白的细胞因子抗体阵列来分析TFH对细胞因子的影响。采用蛋白质印迹法检测TFH对STAT1,STAT4和STAT5信号通路的影响。与正常对照组相比,TFH可以明显增强NK92-MI细胞对K562细胞的细胞毒性,上调NKp44,NKp46,穿孔素和颗粒酶B的表达。TFH可以上调IL-1α,IL-2,IL-7, IL-15,CSF-2,CSF-3,MCP-1,MIG,IFN-γ,TNF-α和TNF-β并下调IL-16,MIP-1β,CX3CL-1和MIF的表达。 TFH可以增加磷酸化STAT1和磷酸化STAT5的表达。结果表明,TFH刺激NK92-MI细胞激活并增强NK92-MI细胞的细胞毒性。

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