کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2130055 1086525 2015 14 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Active invadopodia of mesenchymally migrating cancer cells contain both β and γ cytoplasmic actin isoforms
کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی تحقیقات سرطان
پیش نمایش صفحه اول مقاله
Active invadopodia of mesenchymally migrating cancer cells contain both β and γ cytoplasmic actin isoforms
چکیده انگلیسی


• β- and γ-actin are present in invadopodia formed by breast cancer cells.
• Both actin isoforms are detected together in a single invadopodium.
• Cells with elevated level of β- or γ-actin form more invadopodia and migrate faster.

Invadopodia are actin-rich protrusions formed by mesenchymally migrating cancer cells. They are mainly composed of actin, actin-associated proteins, integrins and proteins of signaling machineries. These protrusions display focalized proteolytic activity towards the extracellular matrix. It is well known that polymerized (F-)actin is present in these structures, but the nature of the actin isoform has not been studied before. We here show that both cytoplasmic actin isoforms, β- and γ-actin, are present in the invadopodia of MDA-MB-231 breast cancer cells cultured on a 2D-surface, where they colocalize with the invadopodial marker cortactin. Invadopodial structures formed by the cells in a 3D-collagen matrix also contain β- and γ-actin. We demonstrate this using isoform-specific antibodies and expression of fluorescently-tagged actin isoforms. Additionally, using simultaneous expression of differentially tagged β- and γ-actin in cells, we show that the actin isoforms are present together in a single invadopodium. Cells with an increased level of β- or γ-actin, display a similar increase in the number and size of invadopodia in comparison to control cells. Moreover, increasing the level of either actin isoforms also increases invasion velocity.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Experimental Cell Research - Volume 339, Issue 2, 10 December 2015, Pages 206–219
نویسندگان
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