Tracking transplanted cells in live animal using upconversion fluorescent nanoparticles

• Published in: Biomaterials Vol. 30; no. 28; pp. 5104 - 5113
• Main Authors: Idris, Niagara Muhammad, Li, Zhengquan, Ye, Lei, Wei Sim, Eugene Kwang, Mahendran, Ratha, Ho, Paul Chi-Lui, Zhang, Yong
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Ltd 01.10.2009
• Subjects: Advanced Basic Science; Animals; Cells, Cultured; Confocal microscopy; Dentistry; Erbium - chemistry; Fluorescent Dyes - analysis; Fluorescent Dyes - chemistry; Fluorides - chemistry; Imaging, Three-Dimensional; Mice; Mice, Inbred C57BL; Microscopy, Confocal; Myoblasts, Skeletal - cytology; Myoblasts, Skeletal - transplantation; Nanoparticle; Nanoparticles - analysis; Nanoparticles - chemistry; Photochemistry; Silicon Dioxide - chemistry; Stem cell; Transplantation; Yttrium - chemistry; Confocal microscopy; Transplantation; Nanoparticle; Stem cell
• ISSN: 0142-9612; 1878-5905
• DOI: 10.1016/j.biomaterials.2009.05.062

Abstract With the emergence of cell transplant as an attractive treatment modality for various diseases, there is a parallel need to track the fate of these cells to assess their therapeutic effectiveness. Here, we report the use of upconversion fluorescent nanoparticles, silica/NaYF4 :Yb,Er, to dynamically track live myoblast cells in vitro and in a living mouse model of cryoinjured hind limb. Nanoparticles loaded into cells were confirmed for its intracellular uptake by confocal imaging, spectrophotometry and inductively coupled plasma analysis. Loaded nanoparticles demonstrated absolute resistance to photobleaching and were applied for dynamic imaging to real time track in vitro cell migratory activity for a continuous 5 h duration using a time-lapse confocal microscope. Direct observation on the direction, speed and cell–cell interaction of migrating cells was clearly visualized. In vivo confocal imaging of nanoparticle-loaded cells intravenously injected into a mouse tail vein showed them flowing in the ear blood vessels. Nanoparticle-loaded cells were also unambiguously identified with superior contrast against a negligible background at least 1300 μm deep in a fully vascularized living tissue upon intramuscular injection. Spatiotemporal migratory activity of the transplanted cells within the three-dimensional living tissue was captured for at least 7 days post-delivery. Direct in vivo visualization of cell dynamics in the native tissue was unobtrusively followed over a 4 h time course and revealed subtle migratory activity of the transplanted cells. With these unique optical properties, we present silica/NaYF4 :Yb,Er nanoparticles as a new fluorescent live cell tracker probe for superior in vitro and in vivo dynamic imaging.