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PMID: 10405175 Published · ppublish English Journal Article

Imaging of caspase-3 activation in HeLa cells stimulated with etoposide using a novel fluorescent probe.

FEBS letters ·Vol. 453 ·No. 3 ·1999-06-25 ·Pages 356-60

Mizukami S, Kikuchi K, Higuchi T, Urano Y, Mashima T, Tsuruo T, Nagano T

Abstract

Microscopic visualization of intracellular enzyme activity can provide information about the physiological role of the enzyme. Caspases are cysteine proteases that have critical roles in the execution of apoptosis. General fluorometric substrates of caspase-3, such as DEVD-MCA, are unsuitable for imaging because they are excited at short wavelength, so we designed and synthesized novel fluorescent probes that are excited at suitable wavelengths for detecting caspase-3 activity in living cells. Using one of these probes, we succeeded in microscopic visualization of caspase-3-like activity within HeLa cells treated with etoposide. The caspase-3-like activity was increased in the cytosol at first, then expanded to the whole cell.

MeSH Terms
Apoptosis Caspase 3 Caspases/isolation & purification,metabolism Enzyme Activation Etoposide/pharmacology Fluorescent Dyes HeLa Cells Humans Microscopy, Fluorescence/methods Topoisomerase II Inhibitors
Chemicals
Fluorescent Dyes Topoisomerase II Inhibitors Etoposide CASP3 protein, human Caspase 3 Caspases
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Mizukami S
Graduate School of Pharmaceutical Sciences, The University of Tokyo, Japan.
Kikuchi K
Higuchi T
Urano Y
Mashima T
Tsuruo T
Nagano T
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1999-06-25
Pages
356-60
Language
English
Region
England
NLM ID
0155157
Subset
IM
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