Small-Molecule Fluorophores To Detect Cell-State Switching in the Context of High-Throughput Screening
EXPRESSION
0301 basic medicine
Time Factors
Muscle Fibers, Skeletal
Drug Evaluation, Preclinical
530
01 natural sciences
PROBES
Cell Line
MYOGENESIS
Myoblasts
Mice
03 medical and health sciences
Predictive Value of Tests
Animals
Enzyme Inhibitors
Fluorescent Dyes
MITOCHONDRIAL-MEMBRANE POTENTIALS
Phosphotransferases
Cell Differentiation
540
0104 chemical sciences
3. Good health
Enzyme Activation
Molecular Weight
DIFFERENTIATION
MAMMALIAN TARGET
Microscopy, Fluorescence
Molecular Probes
LIBRARY
RAPAMYCIN
DOI:
10.1021/ja077656d
Publication Date:
2008-03-08T10:00:35Z
AUTHORS (9)
ABSTRACT
A small molecule capable of distinguishing the distinct states resulting from cellular differentiation would be of enormous value, for example, in efforts aimed at regenerative medicine. We screened a collection of fluorescent small molecules for the ability to distinguish the differentiated state of a mouse skeletal muscle cell line. High-throughput fluorescence-based screening of C2C12 myoblasts and myotubes resulted in the identification of six compounds with the desired selectivity, which was confirmed by high-content screening in the same cell states. The compound that resulted in the greatest fluorescence intensity difference between the cell states was used as the screening agent in a pilot screen of 84 kinase inhibitors, each present in four doses, for inhibition of myogenesis. Of the kinase inhibitors, 17 resulted in reduction of fluorescence at one or more concentrations; among the "hits" included known inhibitors of myogenesis, confirming that this compound is capable of detecting the differentiated myotube state. We suggest that the strategy of screening for screening agents reported here may be extended more broadly in the future.
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CITATIONS (49)
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