Please use this identifier to cite or link to this item: https://doi.org/10.1021/acsami.8b19391
Title: Visualize Embryogenesis and Cell Fate Using Fluorescent Probes with Aggregation-Induced Emission
Authors: Hu, Fang
Manghnani, Purnima Naresh
KENRY 
FENG GUANGXUE 
Wu, Wenbo
Teh, Cathleen
LIU BIN 
Keywords: Science & Technology
Technology
Nanoscience & Nanotechnology
Materials Science, Multidisciplinary
Science & Technology - Other Topics
Materials Science
aggregation-induced emission
small molecule
bright signals
embryonic cell
zebrafish lineage tracing
cell entrapped
INTRACELLULAR INJECTION
ANTIBACTERIAL ACTIVITY
LINEAGE ANALYSIS
LUMINOGENS
Issue Date: 30-Jan-2019
Publisher: American Chemical Society
Citation: Hu, Fang, Manghnani, Purnima Naresh, KENRY, FENG GUANGXUE, Wu, Wenbo, Teh, Cathleen, LIU BIN (2019-01-30). Visualize Embryogenesis and Cell Fate Using Fluorescent Probes with Aggregation-Induced Emission. ACS Applied Materials and Interfaces 11 (4) : 3737-3744. ScholarBank@NUS Repository. https://doi.org/10.1021/acsami.8b19391
Abstract: Horseradish peroxidase (HRP) and fluorogen-dextran conjugate are tracers extensively used for injection-based lineage tracing. However, HRP is sensitive to proteolytic digestion, whereas the high-molecular-weight dextran may have antigenicity. Small molecular tracers can overcome these problems, but they usually diffuse from labeled cells, causing inaccurate information. Herein, we developed a small-molecular-weight fluorogen with aggregation-induced emission (AIEgen) for embryonic cell tracing with strong signals against tracer dilution caused by cell division. Once injected into the ancestor cells, the AIEgen can be entrapped in the cells without leakage because of the two hydrophilic and neutral arms. Consequently, it can specifically trace the progenies of the treated ancestor cells. More importantly, the operating concentration of AIEgen can be much higher than that of fluorogens with aggregation-caused quenching, which provides bright signals in daughter cells during embryonic cell tracing, thus overcoming the problem of fast signal degradation typically encountered with the use of traditional cell tracers.
Source Title: ACS Applied Materials and Interfaces
URI: https://scholarbank.nus.edu.sg/handle/10635/170709
ISSN: 1944-8244
1944-8252
DOI: 10.1021/acsami.8b19391
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