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| 9: Cytokine. 1998 Sep;10(9):645-53. |
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Activation of interleukin-1beta-converting enzyme by
nigericin is independent of apoptosis.
Watanabe N, Kawaguchi M, Kobayashi Y.
Department of Biomolecular Science, Faculty of Science, Toho University,
Chiba, Japan.
Interleukin-1beta-converting enzyme (ICE) is believed to be one of the key
proteases involved in apoptosis. Since the precursor form of interleukin-1beta
(pre-IL-1beta) is one of the well known substrates for ICE, and a
potassium/proton ionophore, nigericin, enhances IL-1beta processing, the
authors hypothesized that nigericin induces apoptosis through the activation
of ICE. In a lipopolysaccharide (LPS)-stimulated and nigericin-treated human
monocytic cell line, THP-1, apoptosis was induced, as assessed as to a
decrease in cell size, chromatin condensation, exposure of phosphatidylserine
and DNA fragmentation. Under exactly the same conditions, nigericin also
induced IL-1beta processing in these cells, which was significantly inhibited
by an ICE inhibitor, acetyl-Tyr-Val-Ala-Asp-CHO. On the contrary, treatment
with this inhibitor at the same concentration did not inhibit
nigericin-induced apoptosis, assessed as to the decrease in cell size,
chromatin condensation and DNA fragmentation. Although apoptosis induced by
nigericin was also observed for LPS-stimulated human peripheral blood
mononuclear cells and a mouse T lymphoma cell line, EL-4, the ICE inhibitor
did not inhibit the apoptosis in the cells. These results suggest that
activated ICE is not involved in the apoptosis induced by nigericin. Since
apopain activity was not augmented under the same conditions, neither ICE nor
apopain may play any role in the nigericin-induced apoptosis. Copyright 1998
Academic Press.
PMID: 9770325 [PubMed - indexed for MEDLINE]
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