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First published online 8 April 2008
doi: 10.1242/jcs.017665
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Research Article |
1 Departament de Biologia Cel·lular i Anatomia Patològica, Facultat de Medicina, Universitat de Barcelona, E-08036 Barcelona, Spain
2 Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, E-08036 Barcelona, Spain
3 Institut de Nanociència i Nanotecnologia (IN2UB), Universitat de Barcelona, E-08036 Barcelona, Spain
4 Laboratorio de Biología Celular, Centro de Investigación Príncipe Felipe and CIBERER, E-46013 Valencia, Spain
* Author for correspondence (e-mail: gegea{at}ub.edu)
Accepted 31 January 2008
In this study, we report the formation of several cytoplasmic inclusion bodies composed of filamentous actin (F-actin) and generated by experimental treatments using depolymerizing or stabilizing actin toxins in neuronal and non-neuronal mammalian cell lines. The actin-stabilizing toxin jasplakinolide (Jpk) induced, in a microtubule-dependent manner, a single, large F-actin aggregate, which contained β- and
-actin, ADF/cofilin, cortactin, and the actin nucleator Arp2/3. This aggregate was tightly associated with the Golgi complex and mitochondria, and was surrounded by vimentin intermediate filaments, microtubules and MAP4. Therefore, the Jpk-induced single, large F-actin aggregate fits the established criteria for being considered an aggresome. Lysosomes and/or autophagic vacuoles, proteasomes and microtubules were found to directly participate in the dissolution of this F-actin aggresome. Finally, the model reported here is simple, highly reproducible and reversible, and it provides an opportunity to test pharmacological agents that interfere with the formation, maintenance and/or disappearance of F-actin-enriched pathological inclusion bodies.
Key words: Actin, Aggresome, Autophagy, Inclusion bodies, Cytoskeleton, Huntingtin, Jasplakinolide, Microtubules, Proteasome