A preliminary study on the proinflammatory mechanisms of Treponema pallidum outer membrane protein Tp92 in human macrophages and HMEC-1 cells

作者：Luo, Xi; Zhang, Xiaohong; Zhao, Tie; Zeng, Tiebing; Liu, Wen; Deng, Meixia; Zhao, Feijun^*

来源：Microbial Pathogenesis, 2017, 110: 176-183.

DOI：10.1016/j.micpath.2017.06.046

• Treponema pallidum
• Inflammatory mechanism
• Tp92
• Membrane protein

Aims: To determine proinfiammatory mechanisms of Treponema pallidum outer membrane protein Tp92 in the early syphilis infection in human macrophages and HMEC-1 cells.
Methods: Recombinant Tp92 protein was used to stimulate target human macrophages and HMEC1 cells. PDTC (Pyrrolidinedithiocarbamic acid), SB202190 and Z-YVAD-FMK were used to block the MyD88/NF-kappa B, MAPK5/p38 and NLRP3/Caspase-1 pathway, respectively. TNF-alpha, IL-1 beta, IL-6, IL-8,NLRP3, casepase-1 were detected by ELISA or Western blot. Lactate dehydrogenase (LDH) activity was measured.
Results: Tp92 protein could significantly induced the secretion of proinflammatory cytokines TNF-alpha, IL-1 beta, IL-6 and IL-8 in HMEC-1 cells, but not in macrophages except IL-8. When MyD88/NF-kappa B pathway was blocked, differences in the secretion of TNF-alpha, IL-6 and IL-1 beta levels and LDH enzyme activity between Tp92 group and Tp92 + PDTC group were not significant (P > 0.05) in HMEC-1 cells and macrophages except IL-8(P < 0.05). When MAPKs/p38 pathway was blocked, differences in the secretion of TNF-alpha, IL-1 beta, IL-6 and IL-8 and LDH enzyme activity both Tp92 group and Tp92 + SB2010190 group were not significant (P > 0.05) in HMEC-1 cells and macrophages. In contrast, when NLRP3/Caspase-1 pathway was blocked with Z-YVAD-FMK, TNF-alpha, IL-6 and IL-1 beta levels, LDH enzyme activity, and Caspase-1 and NLRP3 protein levels were significantly declined (P < 0.05) in HMEC-1 cells except IL-8(P > 0.05). The LDH enzyme activity in macrophages was decreased before and after Z-YVAD-FMK blocking (P < 0.05),however, differences in the secretion of TNF-alpha, IL-1 beta, IL-6 and IL-8 between Tp92 group and Tp92+Z-YVAD-FMK group in macrophages were not significant (P > 0.05).
Conclusions: Tp92 protein may promote proinflammatory cytokines TNF-alpha, IL-1 beta, IL-6 secretion of HMEC-1 cells, but not in macrophages, and increase the LDH enzyme activity of HMEC-1 cells and macrophages through NLRP3/Caspase-1 pathway. However, Tp92 protein may promote IL-8 secretion of HMEC-1 cells and macrophages through MyD88/NF-kappa B pathway.

• 出版日期2017-9
• 单位南华大学