Journal of Bacteriology & Parasitology

Mechanisms related to the up-regulation of IL-10 expression of dendritic cells by parasite-derived molecule Sj16 from Schistosoma japonicum

International Conference on Parasitology

August 24-26, 2015 Philadelphia, USA

Xi Sun1, Fan Yang1, Jia Shen1, Zhen Liu1, Jinyi Liang1, Huanqin Zheng1, Mingqiu Fung2 and Zhongdao Wu1

1Sun Yat-sen University, China 2Chinese University of Hong Kong, China

Scientific Tracks Abstracts: J Bacteriol Parasitol

Abstract:

Schistosomes are parasitic worms that flourish in the human host despite the development of a pronounced immune response. Understanding how the immune system deals with such pathogens is still a daunting challenge. Initiative regulation of host immune response by releasing some schistosome-derived molecules is an important mechanism of immune evasion of Schistsoma japonicum. Previously, our groups have identified a 16-kD secretory protein, Sj16, from Schistosoma japonicum. Sj16 is produced and secreted by all stages of the parasite and confirmed as an important protein in the alleviation of inflammation damage when the cercariae is penetrated into the skin and was closely involved in the immune escape of the schistosomasis. Using recombinant Sj16 (rSj16) protein expressed from E. coli, we demonstrated that this recombinant protein has a potent strong immuno-modulation effect and significantly alleviate rat Adjuvant-Induced Arthritis (AA). Recently, our study have observed that immature DC pulsed with rSj16 can induce significantly IL-10 production and T-helper 2(Th2)-type responses which not show an increase in expression of co-stimulatory molecules or cytokines while their LPS-induced activation, including expression of MHC-II and co-stimulatory molecules as well as IL-12 production is also suppressed. However, since there are no known homologs of Sj16 in metazoans outside the Schistosoma genus, the relationship between Sj16â??s function and IL-10 production are unclear. Hence, in the present study, using antibody neutralization experiment and IL-10-deficent (IL-10 Knockout) mice, we further confirmed that the inhibitory effect of rSj16 on LPS-induced BMDCs is due to its induction of IL- 10 production. To understand how rSj16 induce the production of IL-10, we analyzed the sequence and revealed two potential Nuclear Localization Signal (NLS) of Sj16. Further studies showed that N-terminal NLS (NLS1) is both necessary and sufficient for translocation of rSj16 to the BMDCâ??s nucleus and important for subsequent induction of IL-10 production and inhibition of BMDCs maturation by rSj16. Taken together, our results suggest that rSj16 enter into the nuclear of host cells using the NLS1 and promote the production of IL-10 which mediates the inhibitory effect of rSj16 on LPS-induced BMDCS.

Biography :

Xi Sun has completed her MD in 2004 from Wannan Medical College and her PhD in 2011 from Zhongshan School of Medicine in Sun Yat-Sen University in China. Now she is an Associate Professor in the Department of Parasitology, Zhongshan School of Medicine in Sun Yat-Sen University. She has published more than 20 papers and currently works on the immune escape of Schistosoma japonicum.

Email: wuzhd@mail.sysu.edu.cn