Zhang Heng, Wu Shanghua, Shi Zhiqiang, Wang Shan, Lu Wei, Wu Yizhen, Sun Pei, Xu Qianming
College of Animal Science and Technology, Anhui Agricultural University, Hefei 230036, China.
College of Animal Science and Technology, Anhui Agricultural University, Hefei 230036, China. *Corresponding author, E-mail:
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2018 Mar;34(3):199-204.
Objective To investigate the effect of rhoptry protein 38 (ROP38) from Toxoplasma gondii (T. gondii) on the maturation of dendritic cells (DCs) by Toll-like receptor 4 (TLR4) induction in vitro. Methods The total RNA from T. gondii RH strain was extracted by guanidine thiocyanate method, and then cDNA was synthesized with reverse transcription reaction. After ROP38 gene was amplified by PCR, the recombinant pGEX-4T-ROP38 was constructed and expressed under IPTG induction. The recombinant ROP38 protein was detected by SDS-PAGE and Western blot analysis. The secondary structure and antigenicity of the ROP38 were predicted through DNAStar8.0 and ProtScale. In vitro, DCs were isolated and cultured for 6 days, then reacted with ROP38 antigen for 2 hours. The CD11c was detected by flow cytometry, and the data were analyzed with ANOVA by SPSS 23.0 software. Results The amplified gene was about 516 bp as expected. The sequence analysis showed that its homology was 99% compared with the reported sequence (XM_002366710.2) from GenBank. It was found that the relative molecular mass (M) of recombinant ROP38 was 45 kD. The prediction of structure indicated that there were 5 α-helices, 5 β-sheets, 5 hydrophilic regions and 8 potential epitopes in ROP38 protein. In vitro, the expression of CD11c on DCs was significantly up-regulated after stimulated with ROP38, and the expression level of CD11c in ROP38 infection group was significantly higher than that of the other groups. Conclusion ROP38 promotes the maturation of DCs mediated by TLR4.
目的 体外研究刚地弓形虫棒状体蛋白38(ROP38)通过Toll样受体4(TLR4)诱导对树突状细胞(DCs)成熟的影响。方法 采用异硫氰酸胍法提取刚地弓形虫RH株的总RNA,然后通过逆转录反应合成cDNA。经PCR扩增ROP38基因后,构建重组pGEX-4T-ROP38并在IPTG诱导下表达。通过SDS-PAGE和Western blot分析检测重组ROP38蛋白。利用DNAStar8.0和ProtScale预测ROP38的二级结构和抗原性。体外分离培养DCs 6天,然后与ROP38抗原反应2小时。通过流式细胞术检测CD11c,并用SPSS 23.0软件进行方差分析。结果 扩增的基因约为516 bp,与预期相符。序列分析表明,其与GenBank报道序列(XM_002366710.2)的同源性为99%。发现重组ROP38的相对分子质量(M)为45 kD。结构预测表明,ROP38蛋白中有5个α螺旋、5个β折叠、5个亲水区和8个潜在表位。体外实验中,ROP38刺激后DCs上CD11c的表达显著上调,ROP感染组CD11c的表达水平显著高于其他组。结论 ROP38促进由TLR4介导的DCs成熟。