Author(s) |
Taylor, Jack
Patio, Kevin
De Rubis, Gabriele
Morris, Micheal B
Evenhuis, Christian
Johnson, Michael
Bebawy, Mary
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Publication Date |
2021-07
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Abstract |
<p>Spectrin is a ubiquitous cytoskeletal protein that provides structural stability and supports membrane integrity. In erythrocytes, spectrin proteolysis leads to the biogenesis of plasma membrane extracellular vesicles (EVs). However, its role in non-erythroid or cancer-derived plasma membrane EVs biogenesis is unknown. This study aims to examine the role of αII-spectrin in malignant and non-malignant plasma membrane vesiculation. We developed a custom, automated cell segmentation plugin for the image processor, Fiji, that provides an unbiased assessment of high resolution confocal microscopy images of the subcellular distribution of αII-spectrin. We show that, in low vesiculating non-malignant MBE-F breast cells, prominent cortical spectrin localises to the cell periphery at rest. In comparison, cortical spectrin is diminished in high vesiculating malignant MCF-7 breast cells at rest. A cortical distribution of spectrin correlates with increased biomechanical stiffness as measured by Atomic Force Microscopy. Furthermore, cortical spectrin can be induced in malignant MCF-7 cells by treatment with known vesiculation modulators including the calcium chelator, BAPTA-AM or the calpain inhibitor II (ALLM). These results demonstrate that the subcellular localisation of spectrin is distinctly different in malignant and non-malignant cells at rest and shows that the redistribution of cortical αII-spectrin to the cytoplasm supports plasma membrane-derived EV biogenesis in malignant cells.</p>
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Citation |
Proteomics, 21(13-14), p. 1-13
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ISSN |
1615-9861
1615-9853
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Link | |
Publisher |
Wiley-VCH Verlag GmbH & Co KGaA
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Title |
Membrane to cytosol redistribution of αII-spectrin drives extracellular vesicle biogenesis in malignant breast cells
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Type of document |
Journal Article
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Entity Type |
Publication
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