Crude protein fraction with high thioredoxin reductase (TrxR) enzyme activity from filarial parasite Setaria cervi counters lipopolysaccharide (LPS)-induced inflammation in macrophages.
Nikhilesh JoardarKuladip JanaSanti P Sinha BabuPublished in: Parasitology research (2022)
Host-parasite interaction has always been an area of interest to the parasite biologists. The complex immune interactions between the parasite and/or the parasite-derived products with the host immune cells determine the fate of the disease biology. Parasitic organisms are widely equipped with a vast array of protective machineries including antioxidant enzymes to withstand the hostile condition inside the host body. The reactive oxygen species (ROS) generated inside the host as a result of parasitic intervention can be endured by the parasite by their own tools to ensure their survival. One such antioxidant enzyme in the filarial parasite that plays a significant role in redox homeostasis, survivability and disease progression is the thioredoxin reductase (TrxR). Herein, we have projected a crude lysate of the bovine filarial parasite Setaria cervi enriched with high TrxR enzyme activity has the capacity to downregulate lipopolysaccharide (LPS)-induced inflammatory macrophages. TrxR-mediated inhibition of the TLR4-NF-κB axis resulting into downregulation of the pro-inflammatory cytokines with concomitant upregulation of the anti-inflammatory cytokines supports the filarial parasite to produce an anti-inflammatory milieu which ultimately promotes worm survivability inside the host and pathogenesis.
Keyphrases
- lps induced
- plasmodium falciparum
- toxoplasma gondii
- inflammatory response
- trypanosoma cruzi
- anti inflammatory
- life cycle
- oxidative stress
- reactive oxygen species
- toll like receptor
- signaling pathway
- randomized controlled trial
- immune response
- poor prognosis
- dna damage
- cell death
- nuclear factor
- small molecule
- high resolution
- gram negative
- protein protein
- amino acid