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Matrix Biol. 2019 Jun 1. pii: S0945-053X(19)30064-2. doi: 10.1016/j.matbio.2019.05.006. [Epub ahead of print]

Covalent cross-linking of basement membrane-like matrices physically restricts invasive protrusions in breast cancer cells.

Author information

1
Department of Mechanical Engineering, Stanford University, Stanford, CA 94305, USA.
2
School of Mechanical Engineering, Purdue University, 585 Purdue Mall, West Lafayette, IN 47907, USA.
3
School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, USA.
4
Weldon School of Biomedical Engineering, Purdue University, 206 S. Martin Jischke Drive, West Lafayette, IN 47907, USA. Electronic address: kimty@purdue.edu.
5
Department of Mechanical Engineering, Stanford University, Stanford, CA 94305, USA. Electronic address: chaudhuri@stanford.edu.

Abstract

The basement membrane (BM) provides a physical barrier to invasion in epithelial tumors, and alterations in the molecular makeup and structural integrity of the BM have been implicated in cancer progression. Invadopodia are the invasive protrusions that enable cancer cells to breach the nanoporous basement membrane, through matrix degradation and generation of force. However, the impact of covalent cross-linking on invadopodia extension into the BM remains unclear. Here, we examine the impact of covalent cross-linking of extracellular matrix on invasive protrusions using biomaterials that present ligands relevant to the basement membrane and provide a nanoporous, confining microenvironment. We find that increased covalent cross-linking of reconstituted basement membrane (rBM) matrix diminishes matrix mechanical plasticity, or the ability of the matrix to permanently retain deformation due to force. Covalently cross-linked rBM matrices, and rBM-alginate interpenetrating networks (IPNs) with covalent cross-links and low plasticity, restrict cell spreading and protrusivity. The reduced spreading and reduced protrusivity in response to low mechanical plasticity occurred independent of proteases. Mechanistically, our computational model reveals that the reduction in mechanical plasticity due to covalent cross-linking is sufficient to mechanically prevent cell protrusions from extending, independent of the impact of covalent cross-linking or matrix mechanical plasticity on cell signaling pathways. These findings highlight the biophysical role of covalent cross-linking in regulating basement membrane plasticity, as well as cancer cell invasion of this confining tissue layer.

KEYWORDS:

Basement membrane; Biomaterials; Breast cancer; Cross-linking; Invadopodia; Invasion

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