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Photostable Fluorescent Organic Dots with Aggregation-induced Emission (AIE Dots) for Noninvasive Long-term Cell Tracing

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Journal Sci Rep
Specialty Science
Date 2013 Jan 30
PMID 23359649
Citations 41
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Abstract

Long-term noninvasive cell tracing by fluorescent probes is of great importance to life science and biomedical engineering. For example, understanding genesis, development, invasion and metastasis of cancerous cells and monitoring tissue regeneration after stem cell transplantation require continual tracing of the biological processes by cytocompatible fluorescent probes over a long period of time. In this work, we successfully developed organic far-red/near-infrared dots with aggregation-induced emission (AIE dots) and demonstrated their utilities as long-term cell trackers. The high emission efficiency, large absorptivity, excellent biocompatibility, and strong photobleaching resistance of the AIE dots functionalized by cell penetrating peptides derived from transactivator of transcription proteins ensured outstanding long-term noninvasive in vitro and in vivo cell tracing. The organic AIE dots outperform their counterparts of inorganic quantum dots, opening a new avenue in the development of fluorescent probes for following biological processes such as carcinogenesis.

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References
1.
Fotos J, Patel V, Karin N, Temburni M, Koh J, Galileo D . Automated time-lapse microscopy and high-resolution tracking of cell migration. Cytotechnology. 2008; 51(1):7-19. PMC: 3449480. DOI: 10.1007/s10616-006-9006-7. View

2.
Lin S, Xie X, Patel M, Yang Y, Li Z, Cao F . Quantum dot imaging for embryonic stem cells. BMC Biotechnol. 2007; 7:67. PMC: 2174930. DOI: 10.1186/1472-6750-7-67. View

3.
Piantavigna S, McCubbin G, Boehnke S, Graham B, Spiccia L, Martin L . A mechanistic investigation of cell-penetrating Tat peptides with supported lipid membranes. Biochim Biophys Acta. 2011; 1808(7):1811-7. DOI: 10.1016/j.bbamem.2011.03.002. View

4.
Kaplan I, Wadia J, Dowdy S . Cationic TAT peptide transduction domain enters cells by macropinocytosis. J Control Release. 2005; 102(1):247-53. DOI: 10.1016/j.jconrel.2004.10.018. View

5.
Jin Y, Jia C, Huang S, ODonnell M, Gao X . Multifunctional nanoparticles as coupled contrast agents. Nat Commun. 2010; 1:41. PMC: 3205955. DOI: 10.1038/ncomms1042. View