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Mechano-responsiveness of Fibrillar Adhesions on Stiffness-gradient Gels

Overview
Journal J Cell Sci
Specialty Cell Biology
Date 2020 May 13
PMID 32393601
Citations 25
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Abstract

Fibrillar adhesions are important structural and adhesive components in fibroblasts, and are required for fibronectin fibrillogenesis. While nascent and focal adhesions are known to respond to mechanical cues, the mechanoresponsive nature of fibrillar adhesions remains unclear. Here, we used ratiometric analysis of paired adhesion components to determine an appropriate fibrillar adhesion marker. We found that active α5β1-integrin exhibits the most definitive fibrillar adhesion localization compared to other proteins, such as tensin-1, reported to be in fibrillar adhesions. To elucidate the mechanoresponsiveness of fibrillar adhesions, we designed a cost-effective and reproducible technique to fabricate physiologically relevant stiffness gradients on thin polyacrylamide (PA) hydrogels, embedded with fluorescently labelled beads. We generated a correlation curve between bead density and hydrogel stiffness, thus enabling a readout of stiffness without the need for specialized knowhow, such as atomic force microscopy (AFM). We find that stiffness promotes growth of fibrillar adhesions in a tensin-1-dependent manner. Thus, the formation of these extracellular matrix-depositing structures is coupled to the mechanical parameters of the cell environment and may enable cells to fine-tune their matrix environment in response to changing physical conditions.

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References
1.
Oudin M, Jonas O, Kosciuk T, Broye L, Guido B, Wyckoff J . Tumor Cell-Driven Extracellular Matrix Remodeling Drives Haptotaxis during Metastatic Progression. Cancer Discov. 2016; 6(5):516-31. PMC: 4854754. DOI: 10.1158/2159-8290.CD-15-1183. View

2.
Caliari S, Burdick J . A practical guide to hydrogels for cell culture. Nat Methods. 2016; 13(5):405-14. PMC: 5800304. DOI: 10.1038/nmeth.3839. View

3.
Elosegui-Artola A, Andreu I, Beedle A, Lezamiz A, Uroz M, Kosmalska A . Force Triggers YAP Nuclear Entry by Regulating Transport across Nuclear Pores. Cell. 2017; 171(6):1397-1410.e14. DOI: 10.1016/j.cell.2017.10.008. View

4.
Sottile J, Hocking D . Fibronectin polymerization regulates the composition and stability of extracellular matrix fibrils and cell-matrix adhesions. Mol Biol Cell. 2002; 13(10):3546-59. PMC: 129965. DOI: 10.1091/mbc.e02-01-0048. View

5.
Goreczny G, Forsythe I, Turner C . Hic-5 regulates fibrillar adhesion formation to control tumor extracellular matrix remodeling through interaction with tensin1. Oncogene. 2018; 37(13):1699-1713. PMC: 5876083. DOI: 10.1038/s41388-017-0074-2. View