Immunopotentiator separated from hot water extract of the seed of Benincasa cerifera Savi (Tohgashi) |
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Authors: | Yoshio Kumazawa Yoko Nakatsuru Akira Yamada Toshio Yadomae Chiaki Nishimura Yasuo Otsuka Kikuo Nomoto |
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Affiliation: | (1) School of Pharmaceutical Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, 108 Tokyo, Japan;(2) Department of Immunology, Medical Institute of Bioregulation, Kyushu University, 812 Fukuoka, Japan;(3) Department of Microbial Chemistry, Tokyo College of Pharmacy, 192-03 Hachi-Ohji, Japan;(4) Oriental Medicine Research Center of The Kitasato Institute, 108 Tokyo, Japan;(5) Present address: Department of Experimental Pathology, Cancer Institute, Kami-Ikebukuro, Toshima-ku, 170 Tokyo, Japan |
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Abstract: | Summary The separation and properties of a new immunopotentiator, Benincasa cerifera mitogen (BCM) fraction, were investigated. BCM fraction was separated from hot water extract of the seed of Benincasa cerifera Savi (Tohgashi) by gel filtration using Sepharose 4B. BCM fraction is a heteropolymer consisting of uronic acid, neutral sugars, protein, and phosphorus. The proliferation and differentiation of murine B cells were markedly stimulated by BCM fraction. The in vitro development of peritoneal macrophages into antitumor macrophages was also activated by the addition of BCM fraction to cultures. BCM fraction augmented the IgM and IgG antibody responses against sheep erythrocytes (SRBC) and the induction of delayed-type footpad reaction against SRBC. The antitumor activity of BCM fraction was observed in terms of prolongation of the survival period of mice bearing Meth A fibrosarcoma. After hydrolysis with 1% acetic acid at 100° C for 4 h, marked mitogenic activity was found in a precipitate composed of 29% neutral sugars, 50% uronic acid, 1% protein, and 0.1% phosphorus. The precipitate did not contain detectable amino sugar. The possibility that the biological activities of BCM fraction may be due to contamination by bacterial lipopoly-saccharide was ruled out on the basis of the results of chemical analysis and of marked mitogenicity noted in C3H/HeJ spleen cell cultures.Abbreviations used: BCM, Benincasa cerifera mitogen; SRBC, sheep erythrocytes; PFC, plaque-forming cells; TNP-HRBC, trinitrophenylated horse erythrocytes; PBA, polyclonal B-cell activation; SI, stimulation index |
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