4.8 Article

Remote Control of Heterodimeric Magnetic Nanoswitch Regulates the Adhesion and Differentiation of Stem Cells

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 140, 期 18, 页码 5909-5913

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.8b03001

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资金

  1. National Natural Science Foundation of China [31570979]
  2. Research Grants Council of Hong Kong [14202215, 14220716]
  3. Health and Medical Research Fund
  4. Food and Health Bureau
  5. Government of the Hong Kong Special Administrative Region [04152836, 03140056]
  6. Shun Hing Institute of Advanced Engineering, The Chinese University of Hong Kong [BME-p3-15]
  7. Chow Yuk Ho Technology Centre for Innovative Medicine, The Chinese University of Hong Kong
  8. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource [NSF ECCS-1542205]
  9. MRSEC program at the Materials Research Center [NSF DMR-1720139]
  10. International Institute for Nanotechnology (IIN)
  11. Keck Foundation
  12. State of Illinois, through the IIN

向作者/读者索取更多资源

Remote, noninvasive, and reversible control over the nanoscale presentation of bioactive ligands, such as Arg-Gly-Asp (RGD) peptide, is highly desirable for temporally regulating cellular functions in vivo. Herein, we present a novel strategy for physically uncaging RGD using a magnetic field that allows safe and deep tissue penetration. We developed a heterodimeric nanoswitch consisting of a magnetic nanocage (MNC) coupled to an underlying RGD-coated gold nanoparticle (AuNP) via a long flexible linker. Magnetically controlled movement of MNC relative to AuNP allowed reversible uncaging and caging of RGD that modulate physical accessibility of RGD for integrin binding, thereby regulating stem cell adhesion, both in vitro and in vivo. Reversible RGD uncaging by the magnetic nanoswitch allowed temporal regulation of stem cell adhesion, differentiation, and mechanosensing. This physical and reversible RGD uncaging utilizing heterodimeric magnetic nanoswitch is unprecedented and holds promise in the remote control of cellular behaviors in vivo.

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