Hot-compressed-water decomposed products from bamboo manifest a selective cytotoxicity against acute lymphoblastic leukemia cells

被引:51
作者
Ando, H
Ohba, H
Sakaki, T
Takamine, K
Kamino, Y
Moriwaki, S
Bakalova, R
Uemura, Y
Hatate, Y
机构
[1] AIST, Single Mol Bioanal Lab, Takamatsu, Kagawa 7610395, Japan
[2] Kagoshima Prefecture Inst Ind Technol, Kagoshima 8995105, Japan
[3] Kyushu Univ, Biochem Lab, Fukuoka 8120053, Japan
[4] Kagoshima Univ, Dept Chem Engn & Appl Chem, Kagoshima 8900065, Japan
关键词
decomposed products from bamboo; cytotoxicity; leukemia cell; xylooligosaccharides;
D O I
10.1016/j.tiv.2004.03.011
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
We examined the effect of hot-compressed-water (HCW) extracted and fractionated bamboo products (named as fractions A and B) on the viability of human cultured cell lines, derived from leukemia patients and human peripheral blood lymphocytes, obtained from normal adults. Fraction A was composed of xylose, xylooligosaccharides and water-soluble lignin, determined by high-performance anion exchange chromatography and spectrophotometry. Fraction B was composed of glucose and celooligosaccharides. It was found that Fraction B expressed a negligible cytotoxic effect against leukemia cells, while Fraction A reduced markedly (in a dose-dependent manner) the viability of leukemia cell lines, derived from acute lymphoblastic leukemia (ALL)Jurkat and MOLT-4. Fraction A did not influence the viability of leukemia cells, derived from myelogenous leukemia (ML-2) or lymphoma (SupT-1), as well as the viability of normal lymphocytes. Furthermore, microscopic examination of ALL-derived cells treated with Fraction A showed typical apoptotic morphological changes such as a condensation of nucleus and membrane blebing, as well as phosphatidylserine (PSer) exposure on the cell surface. The effect of decomposed products of commercially available xylan against ALL-derived Jurkat cells was significantly lower than that of Fraction A. These results suggest that the cytotoxic effect of Fraction A may be attributed to apoptosis, induced by xylooligosaccharides and it is specific for ALL-derived cells. We speculate that the water-soluble lignin is an important factor, potentiating the cytotoxic effect of xylan in HCW-extracts from bamboo. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:765 / 771
页数:7
相关论文
共 33 条
  • [21] Biological activities of the lectin, abrin-a, against human lymphocytes and cultured leukemic cell lines
    Moriwaki, S
    Ohba, H
    Nakamura, O
    Sallay, I
    Suzuki, M
    Tsubouchi, H
    Yamasaki, N
    Itoh, K
    [J]. JOURNAL OF HEMATOTHERAPY & STEM CELL RESEARCH, 2000, 9 (01): : 47 - 53
  • [22] MEASUREMENT OF XYLANASE ACTIVITY WITH INSOLUBLE XYLAN SUBSTRATE
    NUMMI, M
    PERRIN, JM
    NIKUPAAVOLA, ML
    ENARI, TM
    [J]. BIOCHEMICAL JOURNAL, 1985, 226 (02) : 617 - 620
  • [23] Inhibitory effect of dideoxyforskolin on cell death induced by ricin, modeccin, diphtheria toxin, and Pseudomonas toxin in MDCK cells
    Oda, T
    Komatsu, N
    Muramatsu, T
    [J]. CELL STRUCTURE AND FUNCTION, 1997, 22 (05) : 545 - 554
  • [24] Relationships between degree of binding, cytotoxicity and cytoagglutinating activity of plant-derived agglutinins in normal lymphocytes and cultured leukemic cell lines
    Ohba, H
    Bakalova, R
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2003, 51 (06) : 451 - 458
  • [25] Cytoagglutination and cytotoxicity of Wheat Germ Agglutinin isolectins against normal lymphocytes and cultured leukemic cell lines -: relationship between structure and biological activity
    Ohba, H
    Bakalova, R
    Muraki, M
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2003, 1619 (02): : 144 - 150
  • [26] Okazaki M., 1990, Bifidobacteria and Microflora, V9, P77
  • [27] TOXIN-INDUCED CELL-LYSIS - PROTECTION BY 3-METHYLADENINE AND CYCLOHEXIMIDE
    SANDVIG, K
    VANDEURS, B
    [J]. EXPERIMENTAL CELL RESEARCH, 1992, 200 (02) : 253 - 262
  • [28] Satoh K, 1999, ANTICANCER RES, V19, P4177
  • [29] Satoh K, 1996, ANTICANCER RES, V16, P2981
  • [30] SHIMIZU N, 1993, BIOL PHARM BULL, V16, P434