Spatial distributions of pericellular stiffness in natural extracellular matrices are dependent on cell-mediated proteolysis and contractility. (15th July 2017)

• Record Type: Journal Article
• Authors: Keating, M.; Kurup, A.; Alvarez-Elizondo, M.; Levine, A.J.; Botvinick, E.
• Is Part Of: Acta biomaterialia. Volume 57(2017)
• Page Start: 304
• Page End: 312
• Publication Date: 2017-07-15
• Subjects: Microrheology -- Cellular remodeling -- Pericellular stiffness -- Tissue mechanics -- Extracellular matrix -- Hydrogel; Biomedical materials -- Periodicals; 610.28
• DOI: 10.1016/j.actbio.2017.05.008
• Languages: English
• ISSNs: 1742-7061

Abstract

Graphical abstract: Abstract: Bulk tissue stiffness has been correlated with regulation of cellular processes and conversely cells have been shown to remodel their pericellular tissue according to a complex feedback mechanism critical to development, homeostasis, and disease. However, bulk rheological methods mask the dynamics within a heterogeneous fibrous extracellular matrix (ECM) in the region proximal to a cell (pericellular region). Here, we use optical tweezers active microrheology (AMR) to probe the distribution of the complex material response function ( α = α ′ + α ″, in units of µm/nN) within a type I collagen ECM, a biomaterial commonly used in tissue engineering. We discovered cells both elastically and plastically deformed the pericellular material. α ′ is wildly heterogeneous, with 1/α ′ values spanning three orders of magnitude around a single cell. This was observed in gels having a cell-free 1/α′ of approximately 0.5 nN/µm. We also found that inhibition of cell contractility instantaneously softens the pericellular space and reduces stiffness heterogeneity, suggesting the system was strain hardened and not only plastically remodeled. The remaining regions of high stiffness suggest cellular remodeling of the surrounding matrix. To test this hypothesis, cells were incubated within the type I collagen gel for 24-h in a media containing a broad-spectrum matrix metalloproteinase (MMP) inhibitor. While pericellular material maintained stiffness asymmetry, stiffness magnitudes were reduced. Dual inhibition demonstrates that the combination of MMP activity and contractility is necessary to establish the pericellular stiffness landscape. This heterogeneity in stiffness suggests the distribution of pericellular stiffness, and not bulk stiffness alone, must be considered in the study of cell-ECM interactions and design of complex biomaterial scaffolds. Statement of Significance: Collagen is a fibrous extracellular matrix (ECM) protein widely used to study cell-ECM interactions. Stiffness of ECM has been shown to instruct cells, which can in turn modify their ECM, as has been shown in the study of cancer and regenerative medicine. Here we measure the stiffness of the collagen microenvironment surrounding cells and quantitatively measure the dependence of pericellular stiffness on MMP activity and cytoskeletal contractility. Competent cell-mediated stiffening results in a wildly heterogeneous micromechanical topography, with values spanning orders of magnitude around a single cell. We speculate studies must consider this notable heterogeneity generated by cells when testing theories regarding the role of ECM mechanics in health and disease.