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长梗绞股蓝寡糖对斑马鱼的免疫调节作用OA

Immunomodulatory effect of Gynostemma longipes oligosaccha-rides in zebrafish

中文摘要英文摘要

目的 探究长梗绞股蓝寡糖(GLO)对长春瑞滨(VNR)诱导的斑马鱼免疫毒性的调节作用.方法 ① 从长梗绞股蓝根部分离制备寡糖组分,采用超高效液相色谱-电雾式检测器和超高效液相色谱-四极杆飞行时间质谱联用技术对其进行表征.② 将受精后4 h(4 hpf)正常孵化的AB野生型斑马鱼胚胎随机分为对照组和GLO 50、100、200、400、800 mg·L-1组,对照组于E3培养液中培养,GLO组暴露于相应浓度GLO溶液中,持续7 d,每天统计存活率,暴露至第5天时于显微镜下观察其形态学变化.③ 选用48 hpf正常孵化的荧光标记中性粒细胞和巨噬细胞的斑马鱼胚胎及120 hpf正常孵化的荧光标记T细胞的斑马鱼胚胎,将其随机分为对照组、模型组、模型+盐酸左旋咪唑(LH)80 mg·L-1组和模型+GLO 50、100、200 mg·L-1组,除对照组外,其余各组加入VNR 200 mg·L-1和相应浓度的药物,对照组加入0.1%DMSO,处理24 h后于共聚焦显微镜下观察斑马鱼尾部中性粒细胞、巨噬细胞和胸腺T细胞荧光强度.④ 选用48 hpf 正常孵化的荧光标记中性粒细胞和巨噬细胞的斑马鱼胚胎,分组及给药同③,处理结束后更换为新鲜E3培养液.随后截断尾部诱导局部急性炎症损伤.损伤6h后在荧光显微镜下统计损伤部位中性粒细胞与巨噬细胞的荧光强度,观察中性粒细胞与巨噬细胞的募集功能.⑤ 选择48 hpf 正常孵化的AB野生型斑马鱼胚胎,分组及给药同③,处理结束后通过转录组测序进行基因本体论(GO)生物过程功能和京都基因与基因组数据库(KEGG)通路富集分析其免疫调节作用机制,并利用RT-qPCR检测Toll样受体4(TLR4)、髓样分化因子88(Myd88)、白细胞介素1β(IL-1β)、IL-6、IL-10、IL-8、肿瘤坏死因子α(TNF-α)和核因子κB p65亚基(NF-κB p65)mRNA水平,Western印迹法检测TLR4蛋白水平,ELISA检测IL-1β和IL-6蛋白水平.结果 ① 成功从长梗绞股蓝中得到寡糖组分,鉴定其为聚合度2~6的寡糖混合物.② GLO在50~200 mg·L-1浓度范围内对斑马鱼胚胎未见明显毒性,400~800 mg·L-1时可引起胚胎畸形,半数致死浓度(LC50)为471.3 mg·L-1.③ 与对照组相比,模型组斑马鱼胚胎中性粒细胞、巨噬细胞和T细胞荧光强度显著降低;与模型组相比,模型+LH组和模型+GLO(50、100、200、400、800 mg·L-1)组上述免疫细胞的荧光强度显著升高.④ 与对照组相比,模型组尾部损伤部位中性粒细胞和巨噬细胞荧光强度显著降低;与模型组相比,模型+LH组、模型+GLO 100和200 mg·L-1组尾部损伤部位上述免疫细胞荧光强度显著升高.⑤ 转录组分析显示,Toll样受体(TLR)信号通路在GO功能富集与KEGG通路中均显著富集.与对照组相比,模型组TLR4、Myd88及其下游炎症因子IL-1β、IL-6、TNF-α、NF-κB p65、IL-10和IL-8的mRNA水平均显著升高;与模型组相比,模型+LH组和模型+GLO 100、200 mg·L-1组TLR4、Myd88及其下游炎症因子IL-1β、IL-6、TNF-α、NF-κB p65、IL-10和IL-8的mRNA水平显著降低.与对照组相比,模型组TLR4、IL-1β和IL-6蛋白水平显著升高;与模型组相比,模型+LH组与模型+GLO 200 mg·L-1组TLR4、IL-1β和IL-6蛋白水平显著降低.结论 在斑马鱼模型中,GLO可通过调控Toll样受体信号通路发挥双重免疫调节作用,既能促进免疫细胞数量与募集功能的恢复,又能抑制过度炎症反应.

OBJECTIVE To investigate the structural characteristics of Gynostemma longipes oligo-saccharide(GLO)and explore their immunomodulatory effects against vinorelbine(VNR)-induced immunotoxicity in a zebrafish model.METHODS ① Oligosaccharide fractions were isolated from the roots of Gynostemma longipes and characterized using ultra-high performance liquid chromatography-charged aerosol detection(UHPLC-CAD)and ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry(UPLC-Q-TOF/MS).② At 4 hours post-fertilization(hpf),normally hatched AB wild-type zebrafish embryos were exposed to GLO at the concentrations of 50,100,200,400 and 800 mg·L-1,while the control group was treated with fresh E3 medium.Mortality was statistically analyzed using GraphPad Prism 10,and morphological changes were observed under a microscope over a 7-day period.③ At 48 hpf,normally hatched zebrafish embryos with fluorescently labeled neutro-phils and macrophages and 120 hpf healthy embryos with fluorescently labeled T cells were divided into control(0.1%DMSO),model(200 mg·L-1 VNR),model+80 mg·L-1 levamisole hydrochloride(LH),and model+GLO(50,100,200 mg·L-1)groups.After 24 h of treatment,fluorescence intensities of neutrophils,macrophages,and T cells were measured using confocal microscopy.④ At 48 hpf,fluores-cently labeled embryos(neutrophils and macrophages)were grouped and treated as described in step③.Following treatment,the medium was replaced with fresh E3,and a tail transection was performed to induce local acute inflammation.At 6 h post-injury,the fluorescence intensities of neutrophils and macrophages at the injury site were quantified under a fluorescence microscope to assess their recruit-ment function.⑤ At 48 hpf,normally hatched AB wild-type zebrafish embryos were grouped and treated as described in step ③.After treatment,transcriptome sequencing was conducted for Gene Ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)enrichment analyses to explore the immunomodulatory mechanisms.The expression levels of Toll-like receptor 4(TLR4),myeloid differen-tiation factor 88(Myd88),interleukin-1β(IL-1β),IL-6,IL-10,IL-8,tumor necrosis factor-α(TNF-α)and nuclear factor κB p65 subunit(NF-κB p65)were measured by RT-qPCR.TLR4 protein levels were detected by Western blotting and IL-1β and IL-6 protein levels by ELISA.RESULTS ① The oligosac-charide fraction was isolated from G.longipes and identified as a mixture of oligosaccharides with degrees of polymerization ranging from 2 to 6.② GLO showed no toxicity to zebrafish embryos at concen-trations of 50-200 mg·L-1,but induced embryonic malformations at 400-800 mg·L-1.Based on embryo survival,an effect-response curve was fitted,and the median lethal concentration(LC50)of GLO was determined to be 471.3 mg·L-1.③ Compared with the control group,fluorescence intensities of neutro-phils,macrophages,and T cells were significantly reduced in the model group,which were markedly restored in model+LH and model+GLO groups.④ Compared with the control group,the fluorescence intensities of neutrophils and macrophages at the injury site of tails were significantly decreased in the model group,suggesting a marked reduction in the recruitment capacity of these immune cells to the injured site.Compared with the model group,the VNR-induced impairment of immune cell recruitment was effectively restored at varying doses in both the LH+model group and the GLO+model groups.⑤ Transcriptomic analysis revealed significant enrichment of the Toll-like receptor signaling pathway in both GO and KEGG annotations.RT-qPCR results showed that,compared with control group,the gene expressions of TLR4,Myd88,and downstream inflammatory factors(IL-1β,IL-6,TNF-α,NF-κB p65,IL-10 and IL-8)were significantly upregulated in the model group.However,these increases were significantly inhibited in model+LH and model+GLO groups.Protein levels of TLR4,IL-1β,and IL-6 were also elevated in the model group compared with the control group,which was significantly attenu-ated in model+LH and model+GLO groups.CONCLUSION This study has confirmed that GLO consist of oligosaccharides with polymerization degrees ranging from 2 to 6,with relatively high contents of disac-charides and pentasaccharides.In a zebrafish model,GLO exert a dual immunomodulatory effect by regulating the Toll-like receptor signaling pathway,promoting the recovery of immune cell numbers and recruitment function while inhibiting excessive inflammatory responses.

王楷迪;高旭;宋娟;张研;洋雯茜;马百平;李强;孙岚;何嘉玲;赵宝全

延边大学农学院,吉林 延吉 133000||军事医学研究院,北京 100850延边大学农学院,吉林 延吉 133000军事医学研究院,北京 100850军事医学研究院,北京 100850||内蒙古民族大学动物科学技术学院,内蒙古 通辽 028000军事医学研究院,北京 100850军事医学研究院,北京 100850延边大学农学院,吉林 延吉 133000军事医学研究院,北京 100850国家卫生健康委科学技术研究所实验动物中心,北京 100853军事医学研究院,北京 100850

医药卫生

长梗绞股蓝寡糖免疫调节斑马鱼Toll样受体信号通路免疫细胞

Gynostemma longipesoligosaccharideimmunomodulationzebrafishToll-like receptor signaling pathwayimmune cells

《中国药理学与毒理学杂志》 2026 (1)

40-52,13

10.3867/j.issn.1000-3002.2026.08804

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