دورية أكاديمية
Impact of C24:0 on actin-microtubule interaction in human neuronal SK-N-BE cells: evaluation by FRET confocal spectral imaging microscopy after dual staining with rhodamine-phalloidin and tubulin tracker green
العنوان: | Impact of C24:0 on actin-microtubule interaction in human neuronal SK-N-BE cells: evaluation by FRET confocal spectral imaging microscopy after dual staining with rhodamine-phalloidin and tubulin tracker green |
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المؤلفون: | Zarrouk, Amira, Nury, Thomas, Dauphin, Aurélien, Frère, Perrine, Riedinger, Jean-Marc, Bachelet, Claude-Marie, Frouin, Frédérique, Moreau, Thibault, Hammami, Mohamed, Kahn, Edmond, Lizard, Gérard |
بيانات النشر: | CIC Edizioni internazionali |
سنة النشر: | 2015 |
المجموعة: | CNR Solar (Scientific Open-access Literature Archive and Repository - Consiglio Nazionale delle Ricerche / National Research Council) |
مصطلحات موضوعية: | 610 Medicina e salute (Classificare qui la tecnologia dei servizi medici) |
الوصف: | Disorganization of the cytoskeleton of neurons has major consequences on the transport of neuro-transmitters via the microtubule network. The interaction of cytoskeleton proteins (actin and tubulin) was studied in neuronal SK-N-BE cells treated with tetracosanoic acid (C24:0), which is cytotoxic and increased in Alzheimer’s disease patients. When SK-N-BE cells were treated with C24:0, mitochondrial dysfunctions and a non-apoptotic mode of cell death were observed. Fluorescence microscopy revealed shrunken cells with perinuclear condensation of actin and tubulin. After staining with rhodamine-phalloidin and with an antibody raised against α-/β-tubulin, modifications of F-actin and α-/β-tubulin levels were detected by flow cytometry. Lower levels of α-tubulin were found by Western blotting. In C24:0-treated cells, spectral analysis and fluorescence recovery after photo-bleaching (FRAP) measured by confocal microscopy proved the existence of fluorescence resonance energy transfer (FRET) when actin and tubulin were stained with tubulin tracker and rhodamine-phalloidin demonstrating actin and tubulin colocalization/interaction. In control cells, no FRET was observed. Our data demonstrate quantitative changes in actin and tubulin, and modified interactions between actin and tubulin in SK-N-BE cells treated with C24:0. They also show that FRET confocal imaging microscopy is an interesting method for specifying the impact of cytotoxic compounds on cytoskeleton proteins. |
نوع الوثيقة: | article in journal/newspaper |
وصف الملف: | text |
اللغة: | English |
العلاقة: | http://eprints.bice.rm.cnr.it/12535/1/portiere.php.pdfTest; Zarrouk, Amira and Nury, Thomas and Dauphin, Aurélien and Frère, Perrine and Riedinger, Jean-Marc and Bachelet, Claude-Marie and Frouin, Frédérique and Moreau, Thibault and Hammami, Mohamed and Kahn, Edmond and Lizard, Gérard (2015) Impact of C24:0 on actin-microtubule interaction in human neuronal SK-N-BE cells: evaluation by FRET confocal spectral imaging microscopy after dual staining with rhodamine-phalloidin and tubulin tracker green. Functional Neurology, 30 (1). pp. 33-46. ISSN 1971-3274 |
الإتاحة: | http://eprints.bice.rm.cnr.it/12535Test/ http://eprints.bice.rm.cnr.it/12535/1/portiere.php.pdfTest http://www.functionalneurology.com/index.php?PAGE=articolo_dett&ID_ISSUE=833&id_article=6980Test |
رقم الانضمام: | edsbas.99E1AEC9 |
قاعدة البيانات: | BASE |
الوصف غير متاح. |