Abstract

Cell adhesion is a crucial biological and biomedical parameter defining cell differentiation, cell migration, cell survival, and state of disease. Because of its importance in cellular function, several tools have been developed in order to monitor cell adhesion in response to various biochemical and mechanical cues. However, there remains a need to monitor cell adhesion and cell-substrate separation with a method that allows real-time measurements on accessible equipment. In this article, we present a method to monitor cell-substrate separation at the single cell level using a plasmonic extraordinary optical transmission substrate, which has a high sensitivity to refractive index changes at the metal-dielectric interface. We show how refractive index changes can be detected using intensity peaks in color channel histograms from RGB images taken of the device surface with a brightfield microscope. This allows mapping of the nonuniform refractive index pattern of a single cell cultured on the plasmonic substrate and therefore high-throughput detection of cell-substrate adhesion with observations in real time.

Highlights

  • Cell adhesion drives crucial cellular functions including differentiation, cell cycle, cell migration, cell survival, and angiogenesis [1,2,3]

  • When a cell binds to a surface, transmembrane proteins called integrins cluster into focal adhesion (FA) complexes that serve to connect the cell to the extracellular matrix (ECM) [6, 7]

  • The red shift of the localized surface plasmon resonance (LSPR) peak with increasing refractive index (RI) is minimal compared to the surface plasmon polariton (SPP)-BW peak and the focus of our analysis is on the longer wavelength SPP-Bloch wave (SPP-BW) peak

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Summary

Introduction

Cell adhesion drives crucial cellular functions including differentiation, cell cycle, cell migration, cell survival, and angiogenesis [1,2,3]. Changes in cell adhesion can define the presence of diseases such as cancer, arthritis, osteoporosis, and atherosclerosis [2]. Tumor cells often exhibit changes in adhesion to an extracellular matrix (ECM) determined by the cell and oncogene type [4, 5]. When a cell binds to a surface, transmembrane proteins called integrins cluster into focal adhesion (FA) complexes that serve to connect the cell to the ECM [6, 7]. Research has shown that chemical and mechanical cues both play crucial roles in determining cellular behavior based on adhesion changes [9,10,11]

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