Publication

Labeling Human Mesenchymal Stem Cells with Gold Nanocages for in vitro and in vivo Tracking by Two-Photon Microscopy and Photoacoustic Microscopy

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Last modified
  • 05/23/2025
Type of Material
Authors
    Yu Shrike Zhang, Georgia Institute of TechnologyYu Wang, Washington University in St. LouisLidai Wang, Washington University in St. LouisYucai Wang, Georgia Institute of TechnologyXin Cai, Washington University in St. LouisChi Zhang, Washington University in St. LouisLihong V. Wang, Washington University in St. LouisYounan Xia, Emory University
Language
  • English
Date
  • 2013-01-01
Publisher
  • Ivyspring International Publisher
Publication Version
Copyright Statement
  • © Ivyspring International Publisher.
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 3
Issue
  • 8
Start Page
  • 532
End Page
  • 543
Grant/Funding Information
  • This work was supported in part by an NIH grant (R01 CA138527) and startup funds from Washington University in St. Louis (to Y.X.).
  • This work was also sponsored by NIH grants (R01 EB000712, R01 EB008085, R01 CA134539, U54 CA136398, R01 CA157277, and R01 CA159959, to L.V.W.).
  • Part of the research was performed at the Alafi Neuroimaging Laboratory of the Hope Center for Neurological Disorders, which was supported by the NIH Neuroscience Blueprint Center Core Grant P30 NS057105.
Supplemental Material (URL)
Abstract
  • Stem cell tracking is a highly important subject. Current techniques based on nanoparticle-labeling, such as magnetic resonance imaging, fluorescence microscopy, and micro-computed tomography, are plagued by limitations including relatively low sensitivity or penetration depth, involvement of ionizing irradiation, and potential cytotoxicity of the nanoparticles. Here we introduce a new class of contrast agents based on gold nanocages (AuNCs) with hollow interiors and porous walls to label human mesenchymal stem cells (hMSCs) for both in vitro and in vivo tracking using two-photon microscopy and photoacoustic microscopy. As demonstrated by the viability assay, the AuNCs showed negligible cytotoxicity under a reasonable dose, and did not alter the differentiation potential of the hMSCs into desired lineages. We were able to image the cells labeled with AuNCs in vitro for at least 28 days in culture, as well as to track the cells that homed to the tumor region in nude mice in vivo.
Author Notes
Keywords
Research Categories
  • Engineering, Biomedical
  • Biology, Cell
  • Biology, Microbiology

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