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Time-dependent intracellular trafficking of FITC-conjugated epigallocatechin-3-O-gallate in L-929 cells.

Bioorganic & medicinal chemistry (2008-10-28)
Dong-Wook Han, Kazuaki Matsumura, Bongju Kim, Suong-Hyu Hyon
RESUMEN

Many in vitro studies about green tea polyphenol, (-)-epigallocatechin-3-O-gallate (EGCG) focused on its pro-apoptotic and anti-proliferative effects on various types of cancer cells, while less attention has been paid to its incorporation into the cytoplasm and nuclear translocation. This study concentrated on the time-dependent intracellular trafficking of EGCG in L-929 cells. EGCG was conjugated with fluorescein-4-isothiocyanate (FITC) via the 3''-OH or 5''-OH group, as confirmed by NMR analysis, and then treated to either suspended or cultured cells. Confocal microscopic observations revealed that FITC-EGCG was clearly seen onto the membrane of suspended cells as well as into the cytoplasm and nucleus within 1h. As an increase in treatment time, it concentrated on the nucleus and then was located at any places of the cells. The cellular uptake of FITC-EGCG in cultured cells was not observed until 1h of culture, but started to be observed after at least 2h. These results imply that although the cellular sensitivity and response to EGCG would be different from those of FITC-EGCG, it would be incorporated into the cytoplasm of cells and further be translocated into the nucleus in a time-dependent manner.

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(−)-Epigallocatechin gallate, ≥95%
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Fluorescein isothiocyanate isomer I, suitable for protein labeling, ≥90% (HPLC), powder
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(−)-Epigallocatechin gallate, ≥80% (HPLC), from green tea
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Fluorescein isothiocyanate isomer I, ≥97.5% (HPLC)
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Fluorescein 5(6)-isothiocyanate, ≥90% (HPLC)
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Fluorescein isothiocyanate isomer I–Celite®, suitable for fluorescent labeling techniques