Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/109482
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Title: Nanomanipulation of ligand nanogeometry modulates integrin/clathrin-mediated adhesion and endocytosis of stem cells
Authors: Yin, B 
Zhang, Q 
Yan, J 
Huang, Y 
Li, C 
Chen, J 
Wen, C 
Wong, SHD 
Yang, M 
Issue Date: 11-Oct-2023
Source: Nano letters, 11 Oct. 2023, v. 23, no. 19, p. 9160-9169
Abstract: Nanosubstrate engineering can be a biomechanical approach for modulating stem cell differentiation in tissue engineering. However, the study of the effect of clathrin-mediated processes on manipulating this behavior is unexplored. Herein, we develop integrin-binding nanosubstrates with confined nanogeometries that regulate clathrin-mediated adhesion- or endocytosis-active signaling pathways for modulating stem fates. Isotropically presenting ligands on the nanoscale enhances the expression of clathrin in cells, thereby facilitating uptake of dexamethasone-loaded nanoparticles (NPs) to boost osteogenesis of stem cells. In contrast, anisotropic ligand nanogeometry suppresses this clathrin-mediated NP entry by strengthening the association between clathrin and adhesion spots to reinforce mechanotransduced signaling, which can be abrogated by the pharmacological inhibition of clathrin. Meanwhile, inhibiting focal adhesion formation hinders cell spreading and enables a higher endocytosis efficiency. Our findings reveal the crucial roles of clathrin in both endocytosis and mechanotransduction of stem cells and provide the parameter of ligand nanogeometry for the rational design of biomaterials for tissue engineering.
Keywords: Cell-substrate interaction
Endocytosis
Ligand nanogeometry
Nanosubstrate engineering
Stem cell differentiation
Publisher: American Chemical Society
Journal: Nano letters 
ISSN: 1530-6984
EISSN: 1530-6992
DOI: 10.1021/acs.nanolett.3c01757
Rights: © 2023 American Chemical Society
This document is the Accepted Manuscript version of a Published Work that appeared in final form in Nano letters, copyright © 2023 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.nanolett.3c01757.
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