Related Experiment Video
Updated: Jun 8, 2025

Visualization of Bacterial Toxin Induced Responses Using Live Cell Fluorescence Microscopy
Published on: October 1, 2012
Bacterial toxins induce non-canonical migracytosis to aggravate acute inflammation
Diyin Li1,2,3, Qi Yang1,2,3, Jianhua Luo2,3,4
1College of Life Sciences, Zhejiang University, Hangzhou, Zhejiang, China.
Abstract:
Migracytosis is a recently described cellular process that generates and releases membrane-bound pomegranate-like organelles called migrasomes. Migracytosis normally occurs during cell migration, participating in various intercellular biological functions. Here, we report a new type of migracytosis induced by small GTPase-targeting toxins. Unlike classic migracytosis, toxin-induced migrasome formation does not rely on cell migration and thus can occur in both mobile and immobile cells. Such non-canonical migracytosis allows the cells to promptly respond to microbial stimuli such as bacterial toxins and effectors and release informative cellular contents in bulk. We demonstrated that C. difficile TcdB3 induces liver endothelial cells and Kupffer cells to produce migrasomes in vivo. Moreover, the migracytosis-defective Tspan9‒/‒ mice show less acute inflammation and lower lethality rate in the toxin challenge assay. Therefore, we propose that the non-canonical migracytosis acts as a new mechanism for mammalian species to sense and exacerbate early immune response upon microbial infections.
Insights
Scientists discovered a new non-migratory cell process, non-canonical migracytosis, triggered by toxins. This process releases cellular contents, potentially exacerbating early immune responses during microbial infections.
Area of Science:
- Cell Biology
- Immunology
- Microbiology
Background:
- Migracytosis is a cellular process generating migrasomes during cell migration.
- It plays roles in intercellular biological functions.
Purpose of the Study:
- To investigate a novel type of migracytosis induced by small GTPase-targeting toxins.
- To understand its role in cellular response to microbial stimuli and immune response.
Main Methods:
- Induction of non-canonical migracytosis using toxins in cell cultures and in vivo.
- Utilizing Tspan9 knockout mice for toxin challenge assays.
Main Results:
- Toxin-induced migrasome formation occurs independently of cell migration.
- Clostridium difficile TcdB3 toxin induces migrasome production in liver endothelial and Kupffer cells.
- Tspan9-deficient mice exhibit reduced inflammation and lethality after toxin exposure.
Conclusions:
- Non-canonical migracytosis is a newly identified mechanism for sensing microbial stimuli.
- This process may contribute to exacerbating early immune responses in mammalian species.
- It offers a potential target for modulating inflammatory responses in infections.
More Related Videos
08:47Induction of Experimental Autoimmune Encephalomyelitis in Mice and Evaluation of the Disease-dependent Distribution of Immune Cells in Various Tissues
Published on: May 8, 2016
07:34Induction of Intestinal Inflammation by Adoptive Transfer of CBir1 TCR Transgenic CD4+ T Cells to Immunodeficient Mice
Published on: December 16, 2021
Related Concept Videos
Inflammation
Defense Against Bacterial Pathogens
Phagocytes
Phagocytes are the frontline soldiers of the immune system. They include neutrophils and macrophages. Neutrophils are the most abundant type of white blood cell and are quickly mobilized to the site of infection. Macrophages are larger cells that patrol...
Chemotaxis and Direction of Cell Migration
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,...
Intracellular Movement of Viruses and Bacteria
Cytotoxic T Cells-mediated Immune Response
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...