Zha Enhui, Dandan Li, Bai Xue, Zhou Tiezhong, Li Yongong, Shenyang Gao, Yue Xiqing
a Department of Food Science and Engineering , Jinzhou Medical University , Jinzhou , China.
b Animal Quarantine Lab , Inspection & Quarantine Technology Center of Hainan Entry-Exit Inspection & Quarantine Bureau , Haikou , China.
Immunopharmacol Immunotoxicol. 2016 Dec;38(6):385-389. doi: 10.1080/08923973.2016.1233978. Epub 2016 Sep 23.
Velvet antler (VA) is recognized as one of the most important Chinese traditional medical herbs. To date, the immunoactivity of the single component of VA is rarely studied though its compound extracts have been well analyzed.
The current study was designed to evaluate the immunomodulatory effects of a recombinant polypeptide (rVAP32) based on the VA of the sika deer by comparison with its natural counterpart (nVAP32).
Splenocytes proliferation and NK-cell cytotoxicity assay was evaluated by the WST-8 colorimetric method. CD4/CD8cell subpopulations regulation was screened by the flowcytometry method and the Th1 or Th2-related cytokine production was measured by ELISA.
In vitro tests showed that both rVAP32 and nVAP32 could significantly stimulate splenocytes proliferation and enhance the NK-cell cytotoxicity and CD4/CD8cell subpopulations when compared with the irrelevant peptide and blank control groups. Also, they demonstrated a significant capacity in up- and down-regulating the expression of Th1- and Th2-related cytokines, respectively. There is no statistically significant difference found between the rVAP32 tested group and nVAP32 control group.
The results obtained herein indicate that rVAP32 has the similar immunomodulatory effects on the immune system of mice as its counterpart nVAP32 in vitro. The further test in vivo is qualified and rVAP32 is promised for developing a new biopharmaceutical product as a substitute for nVAP32.
鹿茸被认为是最重要的中国传统草药之一。尽管鹿茸的复方提取物已得到充分分析,但迄今为止,其单一成分的免疫活性研究较少。
本研究旨在通过与天然对应物(nVAP32)比较,评估基于梅花鹿鹿茸的重组多肽(rVAP32)的免疫调节作用。
采用WST-8比色法评估脾细胞增殖和NK细胞细胞毒性测定。通过流式细胞术筛选CD4/CD8细胞亚群调节,并通过ELISA测定Th1或Th2相关细胞因子的产生。
体外试验表明,与无关肽组和空白对照组相比,rVAP32和nVAP32均能显著刺激脾细胞增殖,增强NK细胞细胞毒性和CD4/CD8细胞亚群。此外,它们分别在上调和下调Th1和Th2相关细胞因子表达方面具有显著能力。rVAP32试验组与nVAP32对照组之间未发现统计学显著差异。
本文获得的结果表明,rVAP32在体外对小鼠免疫系统具有与天然对应物nVAP32相似的免疫调节作用。体内进一步试验合格,rVAP32有望开发成为替代nVAP32的新型生物制药产品。