journal article·2022-06

Combined Effect of Matrix Topography and Stiffness on Neutrophil Shape and Motility

Baeckkyoung Sung, Deok‐Ho Kim, Min‐Ho Kim, Daniele Vigolo

Advanced Biology· Volume 6· Issue 6
Publisher page

Abstract

Abstract The crawling behavior of leukocytes is driven by the cell morphology transition, which is a direct manifestation of molecular motor machinery. The topographical anisotropy and mechanical stiffness of the substrates are the main physical cues that affect leukocytes’ shape generation and migratory responses. However, their combined effects on the cell morphology and motility have been poorly understood, particularly for neutrophils, which are the fastest reacting leukocytes against infections and wounds. Here, spatiotemporally correlated physical parameters are shown, which determine the neutrophil shape change during migratory processes, in response to surface topography and elasticity. Guided crawling and shape generation of individual neutrophils, activated by a uniform concentration of a chemoattractant, are analyzed by adopting elasticity‐tunable micropatterning and live cell imaging techniques. Whole cell‐level image analysis is performed based on a planar geometric quantification of cell shape and motility. The findings show that the pattern anisotropy and elastic modulus of the substrate induce synergic effects on the shape anisotropy, deformability, and polarization/alignment of crawling neutrophils. How the morphology–motility relationship is affected by different surface microstructures and stiffness is demonstrated. These results imply that the neutrophil shape‐motility correlations can be utilized for controlling the immune cell functions with predefined physical microenvironments.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Cellular Mechanics and Interactions · Cell Adhesion Molecules Research · 3D Printing in Biomedical Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

KIST Europe Forschungsgesellschaft mbH 66123 Saarbrücken Germany

Division of Energy & Environment Technology University of Science & Technology Daejeon 34113 Republic of Korea

Department of Bioengineering Johns Hopkins University Baltimore MD 21205 USA

Department of Biological Sciences Kent State University Kent OH 44242 USA

School of Chemical Engineering University of Birmingham Birmingham B15 2TT UK

School of Biomedical Engineering The University of Sydney Sydney NSW 2006 Australia

The University of Sydney Nano Institute University of Sydney Sydney NSW 2006 Australia

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