Magnetic Control and Real-Time Monitoring of Stem Cell Differentiation by the Ligand Nanoassembly

Sungkyu Lee, Myeong Soo Kim, Kapil D. Patel, Hyojun Choi, Ramar Thangam, Jinho Yoon, Thomas Myeongseok Koo, Hee Joon Jung, Sunhong Min, Gunhyu Bae, Yuri Kim, Seong Beom Han, Nayeon Kang, Minjin Kim, Na Li, Hong En Fu, Yoo Sang Jeon, Jae Jun Song, Dong Hwee Kim, Steve ParkJeong Woo Choi, Ramasamy Paulmurugan, Yun Chan Kang, Heon Lee, Qiang Wei, Vinayak P. Dravid, Ki Bum Lee*, Young Keun Kim*, Heemin Kang*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

31 Citations (Scopus)

Abstract

Native extracellular matrix (ECM) exhibits dynamic change in the ligand position. Herein, the ECM-emulating control and real-time monitoring of stem cell differentiation are demonstrated by ligand nanoassembly. The density of gold nanoassembly presenting cell-adhesive Arg-Gly-Asp (RGD) ligand on Fe3O4 (magnetite) nanoparticle in nanostructures flexibly grafted to material is changed while keeping macroscale ligand density invariant. The ligand nanoassembly on the Fe3O4 can be magnetically attracted to mediate rising and falling ligand movements via linker stretching and compression, respectively. High ligand nanoassembly density stimulates integrin ligation to activate the mechanosensing-assisted stem cell differentiation, which is monitored via in situ real-time electrochemical sensing. Magnetic control of rising and falling ligand movements hinders and promotes the adhesion-mediated mechanotransduction and differentiation of stem cells, respectively. These rising and falling ligand states yield the difference in the farthest distance (≈34.6 nm) of the RGD from material surface, thereby dynamically mimicking static long and short flexible linkers, which hinder and promote cell adhesion, respectively. Design of cytocompatible ligand nanoassemblies can be made with combinations of dimensions, shapes, and biomimetic ligands for remotely regulating stem cells for offering novel methodologies to advance regenerative therapies.

Original languageEnglish
Article number2102892
JournalSmall
Volume17
Issue number41
DOIs
Publication statusPublished - 14 Oct 2021
Externally publishedYes

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