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Published on: August 23, 2018
Mode of action of parasporin-4, a cytocidal protein from Bacillus thuringiensis
Shiro Okumura1, Hiroyuki Saitoh, Tomoyuki Ishikawa
1Fukuoka Industrial Technology Centre, 1465-5 Aikawa, Kurume, Fukuoka 839-0861, Japan. sokumura@fitc.pref.fukuoka.jp
Abstract:
Parasporin-4 (PS4) is a cytotoxic protein produced by Bacillus thuringiensis strain A1470. It exhibits specific cytotoxicity against human cancer cell lines, CACO-2, Sawano, and MOLT-4 cells, in particular. When cells were administrated with PS4, cell swelling and nuclear shrinkage were induced, and, the ballooned cells burst within 24 h. PSI-BLAST search showed that the protein shared homology not only with B. thuringiensis Cry toxins but also with aerolysin-type β-pore-forming toxins. Circular dichroism measurements suggested that PS4 was a β-sheet-rich protein. PS4 aggregated into oligomers on the plasma membrane of PS4-susceptible CACO-2 cells, but not on that of PS4-resistant HeLa cells. Leakage of lactate dehydrogenase and influx of extracellular FITC-dextrans were observed only in susceptible cells. The activation of effectors caspase 3 and/or 7 was not observed in PS4-treated CACO-2 cells. It was shown that cytotoxicity of the PS4 against CACO-2 cells was exhibited when treated by cyclodextrin which induces cholesterol depletion. These results suggest that PS4 is a unique β-pore-forming toxin with a cholesterol-independent activity.
Insights
Bacillus thuringiensis produces Parasporin-4 (PS4), a cytotoxic protein targeting cancer cells. This unique beta-pore-forming toxin exhibits cholesterol-independent activity, causing cell lysis without activating caspases.
Area of Science:
- Microbiology
- Molecular Biology
- Biochemistry
Background:
- Parasporin-4 (PS4) is a cytotoxic protein from Bacillus thuringiensis.
- It demonstrates specific toxicity towards human cancer cell lines like CACO-2, Sawano, and MOLT-4.
Purpose of the Study:
- To investigate the mechanism of PS4 cytotoxicity.
- To determine the structural and functional properties of PS4.
Main Methods:
- PSI-BLAST for homology search.
- Circular dichroism for structural analysis.
- Cell-based assays to assess cytotoxicity and membrane integrity.
Main Results:
- PS4 induces cell swelling, nuclear shrinkage, and cell bursting.
- PS4 shares homology with Cry toxins and aerolysin-type toxins.
- PS4 forms aggregates on susceptible cell membranes and causes LDH leakage.
- Cytotoxicity is observed even with cholesterol depletion, indicating cholesterol-independent activity.
Conclusions:
- PS4 is a novel beta-pore-forming toxin.
- Its cytotoxic mechanism is distinct from typical pore-forming toxins and operates independently of cholesterol.
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