Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/61214
Title: Membrane to cytosol redistribution of αII-spectrin drives extracellular vesicle biogenesis in malignant breast cells
Contributor(s): Taylor, Jack (author); Patio, Kevin (author); De Rubis, Gabriele (author); Morris, Micheal B (author); Evenhuis, Christian (author); Johnson, Michael (author); Bebawy, Mary  (author)orcid 
Publication Date: Jul-2021
Publisher: Wiley-VCH Verlag GmbH & Co KGaA
Place of Publication: Germany
DOI: 10.1002/pmic.202000091
Handle Link: https://hdl.handle.net/1959.11/61214
ISSN: 1615-9861
1615-9853
Source of Publication: Proteomics, 21(13-14), p. 1-13
Abstract: 

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.

Publication Type: Journal Article
Fields of Research (FoR) 2020: 3104 Evolutionary biology
Socio-Economic Objective (SEO) 2020: TBD
HERDC Category Description: C1 Refereed Article in a Scholarly Journal
Peer Reviewed: Yes
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