Related Experiment Video
Updated: Feb 13, 2026

QTL Mapping and CRISPR/Cas9 Editing to Identify a Drug Resistance Gene in Toxoplasma gondii
Published on: June 22, 2017
Exosomes derived from Toxoplasma gondii stimulate an inflammatory response through JNK signaling pathway
Yawen Li1, Fangming Xiu2, Zezhong Mou3
1Department of Pathogen Biology, School of Basic Medical Sciences, Shandong University, Jinan, PR China.
Aim:
Exosomes are nanoscale membranous vesicles secreted by most cell types able to transfer bioactive molecules among cells, which play crucial roles in intercellular communication. We characterized the exosomes derived from Toxoplasma gondii and detected the immune response in macrophages.
Methods:
We used transmission electron microscopy, nanotracking analysis and western blotting to identify T. gondii exosomes. Functional experiments were performed in RAW264.7 cells for the induction of cytokines, MAPKs (p38 MAPK, ERK 1/2 and c-Jun N-terminal kinase [JNK]), mRNAs and nuclear translocation of phosphorylated JNK protein.
Results:
JNK pathway was activated by T. gondii exosomes, and the production of IL-12, IFN-γ and TNF-α was significantly increased in macrophages.
Conclusion:
Our findings demonstrated that T. gondii exosomes elicit innate immune through JNK activation, which could provide new insight into the essential regulators of host-pathogen interactions.
Insights
Toxoplasma gondii exosomes activate the JNK pathway in macrophages, increasing innate immune responses. This highlights their role in host-pathogen interactions.
Area of Science:
- Cell Biology
- Immunology
- Parasitology
Background:
- Exosomes are key mediators of intercellular communication, transferring bioactive molecules between cells.
- Toxoplasma gondii, an intracellular parasite, interacts extensively with host cells.
Purpose of the Study:
- To characterize exosomes derived from Toxoplasma gondii.
- To investigate the immune response elicited by T. gondii exosomes in macrophages.
Main Methods:
- Exosome identification using transmission electron microscopy, nanotracking analysis, and western blotting.
- Functional assays in RAW264.7 cells to assess cytokine and mRNA induction.
- Analysis of MAPK pathway activation, including JNK phosphorylation and translocation.
Main Results:
- T. gondii exosomes were successfully identified and characterized.
- Activation of the JNK pathway was observed in macrophages upon exposure to T. gondii exosomes.
- Significant increases in IL-12, IFN-γ, and TNF-α production were detected.
Conclusions:
- T. gondii exosomes stimulate innate immunity via JNK pathway activation.
- These findings offer new insights into the regulatory mechanisms governing host-pathogen interactions during T. gondii infection.
More Related Videos
09:56Toxoplasma gondii Cyst Wall Formation in Activated Bone Marrow-derived Macrophages and Bradyzoite Conditions
Published on: August 12, 2010
09:49Determination of Chemical Inhibitor Efficiency against Intracellular Toxoplasma Gondii Growth Using a Luciferase-Based Growth Assay
Published on: April 29, 2020
Related Concept Videos
Inflammatory Response
Inflammation can be triggered by various stimuli, such as impact, abrasion, chemical irritation, infections, and extreme hot or cold temperatures. These can damage cells and connective tissue fibers,...
Inflammatory Response II: Inflammatory Exudate and Tissue Repair
The typical wound exudate is odorless, transparent, straw-colored, thin, and watery. Exudate, however, can differ depending on the state of wound healing. Likewise, the...
Notch Signaling Pathway
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
Hedgehog Signaling Pathway
Interactions Between Signaling Pathways
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
Inflammatory Response I: Vascular and Cellular