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Enhancement of Ca(2+)‐dependent Endonuclease Activity in L1210 Cells during Apoptosis Induced by 1‐β‐D‐Arabinofuranosylcytosine: Possible Involvement of Activating Factor(s)

Internucleosomal DNA fragmentation and morphological changes in nuclei typical of apoptosis were observed in L1210 cells incubated with 1.0 μg/ml of 1‐β‐D‐arabinofuranosylcytosine (ara‐C). To investigate the mechanisms involved, we examined the activities of endogenous endonucleases in nuclei and cy...

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Detalles Bibliográficos
Autores principales: Takauji, Rumiko, Yoshida, Akira, Iwasaki, Hiromichi, Tohyama, Kaoru, Ueda, Takanori, Nakamura, Toru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920892/
https://www.ncbi.nlm.nih.gov/pubmed/7559086
http://dx.doi.org/10.1111/j.1349-7006.1995.tb02452.x
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author Takauji, Rumiko
Yoshida, Akira
Iwasaki, Hiromichi
Tohyama, Kaoru
Ueda, Takanori
Nakamura, Toru
author_facet Takauji, Rumiko
Yoshida, Akira
Iwasaki, Hiromichi
Tohyama, Kaoru
Ueda, Takanori
Nakamura, Toru
author_sort Takauji, Rumiko
collection PubMed
description Internucleosomal DNA fragmentation and morphological changes in nuclei typical of apoptosis were observed in L1210 cells incubated with 1.0 μg/ml of 1‐β‐D‐arabinofuranosylcytosine (ara‐C). To investigate the mechanisms involved, we examined the activities of endogenous endonucleases in nuclei and cytoplasm. Both fractions of control cells contained Ca(2+) ‐dependent endonuclease which was capable of mediating internucleosomal DNA fragmentation. The assay system using two kinds of target substrates, i.e., nuclear chromatin of CCRF‐CEM cells and naked DNA purified from the same cells, revealed that the activity of Ca(2+)‐dependent endonuclease was enhanced in the crude nuclear extracts of cells treated with 1.0 μg/ml of ara‐C for 24 h or 48 h. The activity was extracted more easily from ara‐C‐treated cells than control cells without sonication of the nuclear fraction. On the other hand, in the cytoplasmic fraction of the cells, the activity towards naked DNA was unchanged, whereas that towards nuclear chromatin was clearly enhanced. These results suggest that internucleosomal DNA fragmentation induced by ara‐C treatment is associated with enhancement and activation of constitutively expressed Ca(2+) ‐dependent endonuclease in L1210 cells.
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spelling pubmed-59208922018-05-11 Enhancement of Ca(2+)‐dependent Endonuclease Activity in L1210 Cells during Apoptosis Induced by 1‐β‐D‐Arabinofuranosylcytosine: Possible Involvement of Activating Factor(s) Takauji, Rumiko Yoshida, Akira Iwasaki, Hiromichi Tohyama, Kaoru Ueda, Takanori Nakamura, Toru Jpn J Cancer Res Article Internucleosomal DNA fragmentation and morphological changes in nuclei typical of apoptosis were observed in L1210 cells incubated with 1.0 μg/ml of 1‐β‐D‐arabinofuranosylcytosine (ara‐C). To investigate the mechanisms involved, we examined the activities of endogenous endonucleases in nuclei and cytoplasm. Both fractions of control cells contained Ca(2+) ‐dependent endonuclease which was capable of mediating internucleosomal DNA fragmentation. The assay system using two kinds of target substrates, i.e., nuclear chromatin of CCRF‐CEM cells and naked DNA purified from the same cells, revealed that the activity of Ca(2+)‐dependent endonuclease was enhanced in the crude nuclear extracts of cells treated with 1.0 μg/ml of ara‐C for 24 h or 48 h. The activity was extracted more easily from ara‐C‐treated cells than control cells without sonication of the nuclear fraction. On the other hand, in the cytoplasmic fraction of the cells, the activity towards naked DNA was unchanged, whereas that towards nuclear chromatin was clearly enhanced. These results suggest that internucleosomal DNA fragmentation induced by ara‐C treatment is associated with enhancement and activation of constitutively expressed Ca(2+) ‐dependent endonuclease in L1210 cells. Blackwell Publishing Ltd 1995-07 /pmc/articles/PMC5920892/ /pubmed/7559086 http://dx.doi.org/10.1111/j.1349-7006.1995.tb02452.x Text en
spellingShingle Article
Takauji, Rumiko
Yoshida, Akira
Iwasaki, Hiromichi
Tohyama, Kaoru
Ueda, Takanori
Nakamura, Toru
Enhancement of Ca(2+)‐dependent Endonuclease Activity in L1210 Cells during Apoptosis Induced by 1‐β‐D‐Arabinofuranosylcytosine: Possible Involvement of Activating Factor(s)
title Enhancement of Ca(2+)‐dependent Endonuclease Activity in L1210 Cells during Apoptosis Induced by 1‐β‐D‐Arabinofuranosylcytosine: Possible Involvement of Activating Factor(s)
title_full Enhancement of Ca(2+)‐dependent Endonuclease Activity in L1210 Cells during Apoptosis Induced by 1‐β‐D‐Arabinofuranosylcytosine: Possible Involvement of Activating Factor(s)
title_fullStr Enhancement of Ca(2+)‐dependent Endonuclease Activity in L1210 Cells during Apoptosis Induced by 1‐β‐D‐Arabinofuranosylcytosine: Possible Involvement of Activating Factor(s)
title_full_unstemmed Enhancement of Ca(2+)‐dependent Endonuclease Activity in L1210 Cells during Apoptosis Induced by 1‐β‐D‐Arabinofuranosylcytosine: Possible Involvement of Activating Factor(s)
title_short Enhancement of Ca(2+)‐dependent Endonuclease Activity in L1210 Cells during Apoptosis Induced by 1‐β‐D‐Arabinofuranosylcytosine: Possible Involvement of Activating Factor(s)
title_sort enhancement of ca(2+)‐dependent endonuclease activity in l1210 cells during apoptosis induced by 1‐β‐d‐arabinofuranosylcytosine: possible involvement of activating factor(s)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920892/
https://www.ncbi.nlm.nih.gov/pubmed/7559086
http://dx.doi.org/10.1111/j.1349-7006.1995.tb02452.x
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