IgM production of lymphocytes from C57BL/6N mice was stimulated by estrogen treated splenic adherent cells

被引:4
作者
Nakaya, M [1 ]
Yamasaki, M [1 ]
Tachibana, H [1 ]
Yamada, K [1 ]
机构
[1] Kyushu Univ, Fac Agr, Dept Biosci & Biotechnol, Div Appl Biol Chem,Lab Food Chem,Higashi Ku, Fukuoka 8128581, Japan
关键词
cell-cell interaction; estrogen receptor; immunoglobulin M; splenocytes;
D O I
10.1016/j.imlet.2004.11.023
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Estrogens have diverse effects on cell growth, differentiation and homeostatic functions, and have been shown to play an important role in regulating immune system. In this study, we examined the effect of 17 beta-estradiol (E2) on antibody production by splenocytes isolated from C57BL/6N mice. Our results suggest that the activation of immunoglobulin (Ig)M production by E2 requires direct cell-cell interaction between adherent and non-adherent cells in mouse splenocyte population, and the primary target of E2 is adherent cell population. In addition, we indicated that ER antagonist ICI 182780 suppressed this enhancing effect of E2. Both ER alpha agonist and ER alpha agonist enhanced IgM production of mouse splenocytes. ERs are expressed on plasma membrane as well as in nucleus. However, a plasma membrane-associated ER specific ligand has no stimulation effect on IgM production. In conclusion, our results indicate that adherent cells stimulated by E2 up-regulate IgM production of lymphocytes through the direct cell-cell interactions, and the enhancing effect of E2 is arouse through ER alpha and ER beta on these cells. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:225 / 231
页数:7
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