p600 stabilizes microtubules to prevent the aggregation of CaMKIIalpha during photoconductive stimulation

• Autorzy: Belzil C. , Ramos T. , Sanada K. , Colicos M. A. , Nguyen M. D.
• Języki publikacji: EN

Abstrakty

EN

The large microtubule-associated/Ca2+-signalling protein p600 (also known as UBR4) is required for hippocampal neuronal survival upon Ca2+ dyshomeostasis induced by glutamate treatment. During this process, p600 prevents aggregation of the Ca2+/calmodulin-dependent kinase IIα (CaMKIIα), a proxy of neuronal death, via direct binding to calmodulin in a microtubuleindependent manner. Using photoconductive stimulation coupled with live imaging of single neurons, we identified a distinct mechanism of prevention of CaMKIIα aggregation by p600. Upon direct depolarization, CaMKIIα translocates to microtubules. In the absence of p600, this translocation is interrupted in favour of a sustained self-aggregation that is prevented by the microtubule-stabilizing drug paclitaxel. Thus, during photoconductive stimulation, p600 prevents the aggregation of CaMKIIα by stabilizing microtubules. The effectiveness of this stabilization for preventing CaMKIIα aggregation during direct depolarization but not during glutamate treatment suggests a model wherein p600 has two modes of action depending on the source of cytosolic Ca2+.

Słowa kluczowe

EN

microtubule; aggregation; calmodulin-dependent kinase IIalpha; photoconductive stimulation; green fluorescent protein; N-methyl-D-aspartate; dimethyl sulphoxide

• Wydawca: -
• Czasopismo: Cellular and Molecular Biology Letters
• Rocznik: 2014
• Tom: 19
• Numer: 3
• Opis fizyczny: p.381-392,fig.,ref.

Twórcy

autor

Belzil C.

• Departments of Clinical Neurosciences, Cell Biology and Anatomy, Biochemistry and Molecular Biology, Hotchkiss Brain Institute, University of Calgary, HMRB 153, 3330 Hospital Drive NW, Calgary, Alberta, Canada, T2N 4N1

autor

Ramos T.

• Departments of Clinical Neurosciences, Cell Biology and Anatomy, Biochemistry and Molecular Biology, Hotchkiss Brain Institute, University of Calgary, HMRB 153, 3330 Hospital Drive NW, Calgary, Alberta, Canada, T2N 4N1

autor

Sanada K.

• Molecular Genetics Research Laboratory, Graduate School of Science, University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan

autor

Colicos M. A.

• Departments of Clinical Neurosciences, Cell Biology and Anatomy, Biochemistry and Molecular Biology, Hotchkiss Brain Institute, University of Calgary, HMRB 153, 3330 Hospital Drive NW, Calgary, Alberta, Canada, T2N 4N1

autor

Nguyen M. D.

• Departments of Clinical Neurosciences, Cell Biology and Anatomy, Biochemistry and Molecular Biology, Hotchkiss Brain Institute, University of Calgary, HMRB 153, 3330 Hospital Drive NW, Calgary, Alberta, Canada, T2N 4N1

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