The epithelial-mesenchymal transition and the cytoskeleton in bioengineered systems

被引:75
|
作者
Leggett, Susan E. [1 ]
Hruska, Alex M. [2 ,3 ]
Guo, Ming [4 ]
Wong, Ian Y. [2 ,3 ]
机构
[1] Princeton Univ, Dept Chem & Biol Engn, William St, Princeton, NJ 08544 USA
[2] Brown Univ, Sch Engn, Ctr Bio Med Engn, 184 Hope St Box D, Providence, RI 02912 USA
[3] Brown Univ, Joint Program Canc Biol, 184 Hope St Box D, Providence, RI 02912 USA
[4] MIT, Dept Mech Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
Actin; Vimentin; Cytoskeleton; Collective migration; Extracellular matrix; BREAST-CANCER CELLS; VIMENTIN INTERMEDIATE-FILAMENTS; EXTRACELLULAR-MATRIX; EXPERIMENTAL COEXPRESSION; MECHANICAL-PROPERTIES; NONLINEAR ELASTICITY; COLLECTIVE INVASION; CONTACT GUIDANCE; TUMOR-METASTASIS; DIVALENT-CATIONS;
D O I
10.1186/s12964-021-00713-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The epithelial-mesenchymal transition (EMT) is intrinsically linked to alterations of the intracellular cytoskeleton and the extracellular matrix. After EMT, cells acquire an elongated morphology with front/back polarity, which can be attributed to actin-driven protrusion formation as well as the gain of vimentin expression. Consequently, cells can deform and remodel the surrounding matrix in order to facilitate local invasion. In this review, we highlight recent bioengineering approaches to elucidate EMT and functional changes in the cytoskeleton. First, we review transitions between multicellular clusters and dispersed individuals on planar surfaces, which often exhibit coordinated behaviors driven by leader cells and EMT. Second, we consider the functional role of vimentin, which can be probed at subcellular length scales and within confined spaces. Third, we discuss the role of topographical patterning and EMT via a contact guidance like mechanism. Finally, we address how multicellular clusters disorganize and disseminate in 3D matrix. These new technologies enable controlled physical microenvironments and higher-resolution spatiotemporal measurements of EMT at the single cell level. In closing, we consider future directions for the field and outstanding questions regarding EMT and the cytoskeleton for human cancer progression.
引用
收藏
页数:24
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