Abstract
Cell–cell adhesions are often subjected to mechanical strains of different rates and magnitudes in normal tissue function. However, the rate-dependent mechanical behavior of individual cell–cell adhesions has not been fully characterized due to the lack of proper experimental techniques and therefore remains elusive. This is particularly true under large strain conditions, which may potentially lead to cell–cell adhesion dissociation and ultimately tissue fracture. In this study, we designed and fabricated a single-cell adhesion micro tensile tester (SCAμTT) using two-photon polymerization and performed displacement-controlled tensile tests of individual pairs of adherent epithelial cells with a mature cell–cell adhesion. Straining the cytoskeleton–cell adhesion complex system reveals a passive shear-thinning viscoelastic behavior and a rate-dependent active stress-relaxation mechanism mediated by cytoskeleton growth. Under low strain rates, stress relaxation mediated by the cytoskeleton can effectively relax junctional stress buildup and prevent adhesion bond rupture. Cadherin bond dissociation also exhibits rate-dependent strengthening, in which increased strain rate results in elevated stress levels at which cadherin bonds fail. This bond dissociation becomes a synchronized catastrophic event that leads to junction fracture at high strain rates. Even at high strain rates, a single cell–cell junction displays a remarkable tensile strength to sustain a strain as much as 200% before complete junction rupture. Collectively, the platform and the biophysical understandings in this study are expected to build a foundation for the mechanistic investigation of the adaptive viscoelasticity of the cell–cell junction.
| Original language | English |
|---|---|
| Article number | e2019347118 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Volume | 118 |
| Issue number | 7 |
| DOIs | |
| State | Published - Feb 16 2021 |
Funding
ACKNOWLEDGMENTS. We acknowledge the funding support from the NSF (Awards 1826135 and 1936065), the NIH National Institutes of General Medical Sciences P20GM113126 (Nebraska Center for Integrated Biomolecular Communication), P20GM104320 (Nebraska Center for the Prevention of Obesity Diseases), P30GM127200 (Nebraska Center for Nanomedicine), 1U54GM115458-01 (Great Plains IDeA-CTR), and R15AR072959. We acknowledge funding support from the Nebraska Collaborative Initiative and EPSCoR FIRST award. Design and fabrication of the TPP structures were conducted at the Center for Nanophase Materials Sciences at Oak Ridge National Laboratory, which is a Department of Energy Office of Science User Facility. C.H. would also like to acknowledge financial support from Nanyang Technological University (Startup Grant M4082352.050) and the Ministry of Education, Singapore, under its Academic Research Fund Tier 1 (M4012229.050). M.D. acknowledges partial support from NIH R01HL154150. We are grateful for the technical assistance of Dr. You Zhou from Center of Biotechnology at University of Nebraska–Lincoln, Dr. Edward Nelson from Nanosurf, and Dr. Benjamin Richter from Nanoscribe.
Keywords
- Cell mechanics | cell–cell junction | stress–strain relationship | stress relaxation