TY - JOUR
T1 - Dynamic Ligand Screening by Magnetic Nanoassembly Modulates Stem Cell Differentiation
AU - Hong, Hyunsik
AU - Min, Sunhong
AU - Koo, Sagang
AU - Lee, Yunjung
AU - Yoon, Jinho
AU - Jang, Woo Young
AU - Kang, Nayeon
AU - Thangam, Ramar
AU - Choi, Hyojun
AU - Jung, Hee Joon
AU - Han, Seong Beom
AU - Wei, Qiang
AU - Yu, Seung Ho
AU - Kim, Dong Hwee
AU - Paulmurugan, Ramasamy
AU - Jeong, Woong-Kyo
AU - Lee, Ki Bum
AU - Hyeon, Taeghwan
AU - Kim, Dokyoon
AU - Kang, Heemin
N1 - Funding Information:
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (No. 2020R1C1C1011038 and 2019R1F1A1060107). This work was also supported by a Korea University Grant. HAADF-STEM imaging was conducted with the support of the Seoul Center in Korea Basic Science Institute (KBSI). This work made use of the EPIC facility of Northwestern University's NUANCE Center, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205), the MRSEC IRG2 program (NSF DMR-1720139) at the Materials Research Center, the International Institute for Nanotechnology (IIN), the Keck Foundation, and the State of Illinois, through the IIN.
Funding Information:
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (No. 2020R1C1C1011038 and 2019R1F1A1060107). This work was also supported by a Korea University Grant. HAADF‐STEM imaging was conducted with the support of the Seoul Center in Korea Basic Science Institute (KBSI). This work made use of the EPIC facility of Northwestern University's NUANCE Center, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS‐1542205), the MRSEC IRG2 program (NSF DMR‐1720139) at the Materials Research Center, the International Institute for Nanotechnology (IIN), the Keck Foundation, and the State of Illinois, through the IIN.
Publisher Copyright:
© 2021 Wiley-VCH GmbH
PY - 2022/1/13
Y1 - 2022/1/13
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85119294794&partnerID=8YFLogxK
U2 - 10.1002/adma.202105460
DO - 10.1002/adma.202105460
M3 - Article
C2 - 34655440
AN - SCOPUS:85119294794
SN - 0935-9648
VL - 34
JO - Advanced Materials
JF - Advanced Materials
IS - 2
M1 - 2105460
ER -