Plasma Membrane Blebbing Is Controlled by Subcellular Distribution of Vimentin Intermediate Filaments

Author:

Chikina Aleksandra S.12ORCID,Zholudeva Anna O.1,Lomakina Maria E.1,Kireev Igor I.3ORCID,Dayal Alexander A.4,Minin Alexander A.4,Maurin Mathieu5,Svitkina Tatyana M.6,Alexandrova Antonina Y.1

Affiliation:

1. N.N. Blokhin National Medical Research Center of Oncology, 24 Kashirskoe Shosse, Moscow 115478, Russia

2. Dynamics of Immune Responses Team, INSERM-U1223 Institut Pasteur, 25-28 Rue du Dr Roux, 75015 Paris, France

3. Department of Biology and A.N. Belozersky Institute of Physico-Chemical Biology, M.V. Lomonosov Moscow State University, 1 Leninskie Gory, Moscow 119992, Russia

4. Institute of Protein Research, Department of Cell Biology, Russian Academy of Sciences, Moscow 119988, Russia

5. Institut Curie, PSL Research University, INSERM U932, 26 rue d’Ulm, 75248 Paris, France

6. Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA

Abstract

The formation of specific cellular protrusions, plasma membrane blebs, underlies the amoeboid mode of cell motility, which is characteristic for free-living amoebae and leukocytes, and can also be adopted by stem and tumor cells to bypass unfavorable migration conditions and thus facilitate their long-distance migration. Not all cells are equally prone to bleb formation. We have previously shown that membrane blebbing can be experimentally induced in a subset of HT1080 fibrosarcoma cells, whereas other cells in the same culture under the same conditions retain non-blebbing mesenchymal morphology. Here we show that this heterogeneity is associated with the distribution of vimentin intermediate filaments (VIFs). Using different approaches to alter the VIF organization, we show that blebbing activity is biased toward cell edges lacking abundant VIFs, whereas the VIF-rich regions of the cell periphery exhibit low blebbing activity. This pattern is observed both in interphase fibroblasts, with and without experimentally induced blebbing, and during mitosis-associated blebbing. Moreover, the downregulation of vimentin expression or displacement of VIFs away from the cell periphery promotes blebbing even in cells resistant to bleb-inducing treatments. Thus, we reveal a new important function of VIFs in cell physiology that involves the regulation of non-apoptotic blebbing essential for amoeboid cell migration and mitosis.

Funder

Russian Science Foundation

National Institutes of Health

Lomonosov Moscow State University Development Program

Publisher

MDPI AG

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