Cytotoxicity Induced byErythrina variegataSerine Proteinase Inhibitors in Tumor Hematopoietic Stem Cell Lines
Author(s) -
Hideki Ohba,
Masaaki Nishikawa,
Makoto Kimura,
Nobuyuki Yamasaki,
Sawako Moriwaki,
Kyogo Itoh
Publication year - 1998
Publication title -
bioscience biotechnology and biochemistry
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.509
H-Index - 116
eISSN - 1347-6947
pISSN - 0916-8451
DOI - 10.1271/bbb.62.1166
Subject(s) - cytotoxicity , jurkat cells , cytotoxic t cell , trypsin , biochemistry , cell culture , biology , microbiology and biotechnology , chemistry , enzyme , in vitro , immunology , t cell , genetics , immune system
Based on the soluble MTT tetrazolium/formazan assay, we evaluated the cytotoxicity of Erythrina variegata proteinase inhibitors in some tumor hematopoietic stem cell lines. Among the proteinase inhibitors, EBI, which belongs to the Bowman-Birk family of inhibitors, was cytotoxic in relatively differentiated cells such as Molt4 and Jurkat derived from acute T lymphoblastic leukemia (T-ALL) cells specifically, but ETIa and ECI, which are classified into Kunitz family inhibitors, did not. It was suggested that the differences in the cytotoxicity might be due to the molecular size of the inhibitors. The succinylation of lysine residue(s) of EBI led to about 50% loss of the trypsin inhibitory activity as compared with the authentic EBI. When Molt4 cells were incubated with this derivative, no significant cytotoxicity was observed. This suggests that the proteinase inhibitory activity might be involved in the cytotoxicity in human tumor cell lines.
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