| Literature DB >> 34655440 |
Hyunsik Hong1, Sunhong Min1, Sagang Koo2,3, Yunjung Lee2,3, Jinho Yoon4, Woo Young Jang5, Nayeon Kang1, Ramar Thangam1, Hyojun Choi1, Hee Joon Jung6,7,8, Seong-Beom Han9, Qiang Wei10, Seung-Ho Yu11, Dong-Hwee Kim9, Ramasamy Paulmurugan12,13, Woong Kyo Jeong5, Ki-Bum Lee4, Taeghwan Hyeon2,3, Dokyoon Kim2,14, Heemin Kang1,15.
Abstract
In native microenvironment, diverse physical barriers exist to dynamically modulate stem cell recruitment and differentiation for tissue repair. In this study, nanoassembly-based magnetic screens of various sizes are utilized, and they are elastically tethered over an RGD ligand (cell-adhesive motif)-presenting material surface to generate various nanogaps between the screens and the RGDs without modulating the RGD density. Large screens exhibiting low RGD distribution stimulate integrin clustering to facilitate focal adhesion, mechanotransduction, and differentiation of stem cells, which are not observed with small screens. Magnetic downward pulling of the large screens decreases the nanogaps, which dynamically suppress the focal adhesion, mechanotransduction, and differentiation of stem cells. Conversely, magnetic upward pulling of the small screens increases the nanogaps, which dynamically activates focal adhesion, mechanotransduction, and differentiation of stem cells. This regulation mechanism is also shown to be effective in the microenvironment in vivo. Further diversifying the geometries of the physical screens can further enable diverse modalities of multifaceted and safe unscreening of the distributed RGDs to unravel and modulate stem cell differentiation for tissue repair.Entities:
Keywords: dynamic RGD screening; magnetic nanoassemblies; stem cell adhesion; stem cell differentiation
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Year: 2021 PMID: 34655440 DOI: 10.1002/adma.202105460
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849