Vimentin Intermediate Filament Rings Deform the Nucleus During the First Steps of Adhesion

被引:27
作者
Terriac, Emmanuel [1 ]
Schuetz, Susanne [2 ]
Lautenschlaeger, Franziska [1 ,2 ]
机构
[1] Leibniz Inst New Mat, Saarbrucken, Germany
[2] Saarland Univ, Fac Nat Sci & Technol, Saarbrucken, Germany
关键词
vimentin; adhesion; nuclear deformation; ring; cell spreading; MOLECULAR-MECHANISMS; CELL MECHANICS; RHOA ACTIVITY; PLECTIN; PHOSPHORYLATION; MICROTUBULES; INTEGRINS; DYNAMICS; DOMAIN; ACTIN;
D O I
10.3389/fcell.2019.00106
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
During cell spreading, cells undergo many changes to their architecture and their mechanical properties. Vimentin, as an integral part of the cell architecture, and its mechanical stability must adapt to the new state of the cell. This study focuses on the structures formed by vimentin during the first steps of cell adhesion. Very early, ball-like structures, or "knots," are seen and often vimentin filaments emerge in the shape of rings around the nucleus. Although intermediate filaments are not known to be associated to motor proteins to form contractile systems, these rings can nonetheless strongly deform the cell nucleus. In the first 6 to 12 h of adhesion, these vimentin knots and rings disappear, and the intermediate filament network returns to the state seen before detachment of the cells. As these vimentin structures are very transient in the early steps of cell spreading, they have rarely been described in the literature. However, they can also be seen during mitosis, which is an event that involves partial detachment and respreading of the cells. Interestingly, the turnover dynamics of vimentin are reduced in both the knots and rings, compared to vimentin in the lamellipodia. It remains to define how the force is transmitted from the ball-like structures to the rings, and to measure the impact of such strong nuclear deformation on gene expression during cell re-spreading and the rearrangement of the vimentin network.
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页数:10
相关论文
共 57 条
[11]   Vimentin Diversity in Health and Disease [J].
Danielsson, Frida ;
Peterson, McKenzie Kirsten ;
Araujo, Helena Caldeira ;
Lautenschlaeger, Franziska ;
Britt Gad, Annica Karin .
CELLS, 2018, 7 (10)
[12]  
Davies JA, 1996, ACTA ANAT, V156, P187
[13]  
Duarte S., 2018, BIORXIV, DOI [10.1101/356642, DOI 10.1101/356642]
[14]   Specific in vivo phosphorylation sites determine the assembly dynamics of vimentin intermediate filaments [J].
Eriksson, JE ;
He, T ;
Trejo-Skalli, AV ;
Härmälä-Braskén, AS ;
Hellman, J ;
Chou, YH ;
Goldman, RD .
JOURNAL OF CELL SCIENCE, 2004, 117 (06) :919-932
[15]   A direct interaction between actin and vimentin filaments mediated by the tail domain of vimentin [J].
Esue, Osigwe ;
Carson, Ashley A. ;
Tseng, Yiider ;
Wirtz, Denis .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (41) :30393-30399
[16]   Cell mechanics and the cytoskeleton [J].
Fletcher, Daniel A. ;
Mullins, Dyche .
NATURE, 2010, 463 (7280) :485-492
[17]   Distribution and ultrastructure of plectin arrays in subclones of rat glioma C-6 cells differing in intermediate filament protein (vimentin) expression [J].
Foisner, R ;
Bohn, W ;
Mannweiler, K ;
Wiche, G .
JOURNAL OF STRUCTURAL BIOLOGY, 1995, 115 (03) :304-317
[18]  
FUCHS E, 1994, ANNU REV BIOCHEM, V63, P345, DOI 10.1146/annurev.bi.63.070194.002021
[19]   Vimentin Intermediate Filaments Template Microtubule Networks to Enhance Persistence in Cell Polarity and Directed Migration [J].
Gan, Zhuo ;
Ding, Liya ;
Burckhardt, Christoph J. ;
Lowery, Jason ;
Zaritsky, Assaf ;
Sitterley, Karlyndsay ;
Mota, Andressa ;
Costigliola, Nancy ;
Starker, Colby G. ;
Voytas, Daniel F. ;
Tytell, Jessica ;
Goldman, Robert D. ;
Danuser, Gaudenz .
CELL SYSTEMS, 2016, 3 (03) :252-+
[20]   EPITHELIA SUSPENDED IN COLLAGEN GELS CAN LOSE POLARITY AND EXPRESS CHARACTERISTICS OF MIGRATING MESENCHYMAL CELLS [J].
GREENBURG, G ;
HAY, ED .
JOURNAL OF CELL BIOLOGY, 1982, 95 (01) :333-339