Immunomodulating activities of polysaccharide fractions from dried safflower petals

被引:32
作者
Wakabayashi, T
Hirokawa, S
Yamauchi, N
Kataoka, T
Woo, JT
Nagai, K
机构
[1] Tokyo Inst Technol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 226, Japan
[2] Yamagata Univ, Fac Educ, Chem Lab, Yamagata 990, Japan
关键词
B cell; Carthamus tinctorius L; cytokine; lipopolysaccharides; macrophages; polysaccharide; safflower;
D O I
10.1023/A:1007947329496
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In the course of screening for immunomodulators, we found a significant blastogenic activity specific for splenic B cells in the extracts of safflower (Carthamus tinctorius L.). Active fractions termed SF1 and SF2 were purified from dried petals of safflower by boiling water extraction, ethanol precipitation and Sepharose CL-2B column chromatography. The elution profiles of the gel filtration indicated that the molecular weight of SF1 and SF2 was estimated to be more than 100 kD. Major components of SF1 and SF2 seem to be polysaccharides, and structural analysis of alditol acetate derivatives by GC-MS revealed some differences between SF1 and SF2 in the sugar component. Biological activities of SF1 and SF2 on B cells and macrophages were examined in comparison with lipopolysaccharides (LPS). SF1 and SF2 induced both the proliferation and the IgM production of B cells to the equivalent level as those induced by LPS. In macrophages, SF1 and SF2 effectively stimulated the production of NO. However, SF1 stimulated the production of IL-1, IL-6, and TNF as much as LPS, while SF2 induced them only weakly or not at all. Thus, these results suggest that SF1 and SF2 activate B cells and macrophages in different mechanisms.
引用
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页码:205 / 211
页数:7
相关论文
共 23 条
[1]  
Brander W.T., 1958, CANCER RES, V18, P347
[2]  
BRANDER WT, 1959, CANCER RES, V19, P673
[3]  
CHIHARA G, 1969, Nature (London), V222, P687
[4]  
CHIHARA G, 1970, CANCER RES, V30, P2776
[5]  
COHEN L, 1995, J IMMUNOL, V155, P5337
[6]   Resistance to endotoxin shock and reduced dissemination of gram-negative bacteria in CD14-deficient mice [J].
Haziot, A ;
Ferrero, E ;
Kontgen, F ;
Hijiya, N ;
Yamamoto, S ;
Silver, J ;
Stewart, CL ;
Goyert, SM .
IMMUNITY, 1996, 4 (04) :407-414
[7]   STIMULATION OF B-LYMPHOCYTES BY LIPOPOLYSACCHARIDES FROM ANAEROBIC-BACTERIA [J].
HOFSTAD, T ;
SKAUG, N ;
SVEEN, K .
CLINICAL INFECTIOUS DISEASES, 1993, 16 :S200-S202
[8]  
ITOH W, 1990, INT J IMMUNOPHARMACO, V12, P225
[9]  
Kalechman Y, 1996, J IMMUNOL, V156, P1101
[10]  
KALECHMAN Y, 1990, J IMMUNOL, V145, P1512