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Published on: February 16, 2015
Cleavage of tensin during cytoskeleton disruption in YTX-induced apoptosis
Mónica Suárez Korsnes1, Dyveke Lem Hetland, Arild Espenes
1The Norwegian School of Veterinary Science, P.O. Box 8146, Dep. No. 0033, Food Safety and Infection Biology Department, Ullevaalsveien 72, Oslo, Norway. Monica.Suarez@veths.no
Abstract:
Yessotoxin (YTX) is a marine algal toxin previously shown to induce apoptosis in L6 and BC3H1 myoblast cell lines. Disassembly of the F-actin cytoskeleton and cleavage of tensin, a cytoskeletal protein localised at the focal adhesion contacts, appear during this apoptotic process. Tensin binds to actin filaments at the focal adhesion contacts and it links the actin cytoskeleton to the extracellular matrix (ECM). This binding occurs via integrin receptors and it makes tensin a potential link between the actin cytoskeleton and signal transduction. This study evaluates disruption in the F-actin cytoskeleton and change of tensin in myoblast cell lines exposed to 100 nM YTX up to 72 h. YTX treatment cleaves tensin and makes it translocate to the cell centre. Tensin has normally a role in the maintenance of cell shape and YTX-treatment may therefore alter the shape of the cells. YTX exposure also induces formation of lamellas associated with pseudopodia. Alternative linkages and cytoskeletal proteins anchoring the actin filaments to focal contacts remain to be identified.
Insights
Yessotoxin (YTX) disrupts the F-actin cytoskeleton and cleaves tensin, a key protein in cell adhesion and shape maintenance. This marine toxin alters myoblast cell structure, leading to potential cell shape changes and lamella formation.
Area of Science:
- Cell Biology
- Toxicology
- Biochemistry
Background:
- Yessotoxin (YTX) is a marine algal toxin.
- YTX induces apoptosis in myoblast cell lines.
- YTX causes F-actin cytoskeleton disassembly and tensin cleavage.
Purpose of the Study:
- To evaluate F-actin cytoskeleton disruption by YTX.
- To assess changes in tensin protein in myoblast cell lines.
- To understand YTX's mechanism of action on cell structure.
Main Methods:
- Exposure of L6 and BC3H1 myoblast cell lines to 100 nM YTX.
- Incubation periods up to 72 hours.
- Analysis of F-actin cytoskeleton and tensin protein localization and cleavage.
Main Results:
- YTX treatment cleaves tensin, causing its translocation to the cell center.
- YTX alters cell shape and induces lamella formation associated with pseudopodia.
- Disruption of the F-actin cytoskeleton and tensin is confirmed.
Conclusions:
- YTX significantly impacts myoblast cell structure by disrupting the F-actin cytoskeleton and altering tensin.
- Tensin cleavage and translocation by YTX suggest a role in YTX-induced apoptosis and cell shape changes.
- Further research is needed to identify alternative proteins involved in focal contact anchoring after YTX exposure.
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