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Effect of estrogens on the interferon-gamma producing cell population of mouse splenocytes.

Identifieur interne : 002D32 ( Main/Exploration ); précédent : 002D31; suivant : 002D33

Effect of estrogens on the interferon-gamma producing cell population of mouse splenocytes.

Auteurs : Mako Nakaya [Japon] ; Hirofumi Tachibana ; Koji Yamada

Source :

RBID : pubmed:16428820

Descripteurs français

English descriptors

Abstract

We examined the effect of 17beta-estradiol (E2) on the cytokine production by mouse splenocytes. The production of interferon-gamma (IFN-gamma) was enhanced by E2 stimulation. E2 increased the number of cells expressing IFN-gamma and the IFN-gamma mRNA expression level in the cells. There were low- and high-level cells expressing IFN-gamma in the population. The natural killer (NK) cells and NKT cells were the low-level cells expressing IFN-gamma, and the number of these cells was increased by E2 stimulation. In addition, it was suggested that the enhancing effect of IFN-gamma production by E2 was mediated through estrogen receptor (ER) alpha, and ERbeta agonist stimulated IFN-gamma production. ERs are expressed on plasma membrane as well as in nucleus. The ligand specific to plasma membrane-associated ER (mER) enhanced the IFN-gamma production. In conclusion, our results indicated that E2 up-regulated the IFN-gamma production by mediating ERalpha, ERbeta and mERs.

DOI: 10.1271/bbb.70.47
PubMed: 16428820


Affiliations:


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Le document en format XML

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<term>Animals</term>
<term>Cells, Cultured</term>
<term>Estradiol (pharmacology)</term>
<term>Estrogen Receptor alpha (agonists)</term>
<term>Estrogen Receptor alpha (metabolism)</term>
<term>Estrogen Receptor beta (agonists)</term>
<term>Estrogen Receptor beta (metabolism)</term>
<term>Gene Expression Regulation (drug effects)</term>
<term>Gene Expression Regulation (genetics)</term>
<term>Interferon-gamma (biosynthesis)</term>
<term>Interferon-gamma (genetics)</term>
<term>Male</term>
<term>Mice</term>
<term>Mice, Inbred C57BL</term>
<term>RNA, Messenger (genetics)</term>
<term>Spleen (drug effects)</term>
<term>Spleen (metabolism)</term>
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<term>ARN messager (génétique)</term>
<term>Animaux</term>
<term>Cellules cultivées</term>
<term>Interféron gamma (biosynthèse)</term>
<term>Interféron gamma (génétique)</term>
<term>Mâle</term>
<term>Oestradiol (pharmacologie)</term>
<term>Rate ()</term>
<term>Rate (métabolisme)</term>
<term>Récepteur alpha des oestrogènes (agonistes)</term>
<term>Récepteur alpha des oestrogènes (métabolisme)</term>
<term>Récepteur bêta des oestrogènes (agonistes)</term>
<term>Récepteur bêta des oestrogènes (métabolisme)</term>
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<term>Souris de lignée C57BL</term>
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<term>Estrogen Receptor alpha</term>
<term>Estrogen Receptor beta</term>
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<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en">
<term>Interferon-gamma</term>
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<term>Interferon-gamma</term>
<term>RNA, Messenger</term>
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<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Estrogen Receptor alpha</term>
<term>Estrogen Receptor beta</term>
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<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Estradiol</term>
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<term>Récepteur alpha des oestrogènes</term>
<term>Récepteur bêta des oestrogènes</term>
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<term>Gene Expression Regulation</term>
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<term>Récepteur bêta des oestrogènes</term>
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<term>Oestradiol</term>
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<front>
<div type="abstract" xml:lang="en">We examined the effect of 17beta-estradiol (E2) on the cytokine production by mouse splenocytes. The production of interferon-gamma (IFN-gamma) was enhanced by E2 stimulation. E2 increased the number of cells expressing IFN-gamma and the IFN-gamma mRNA expression level in the cells. There were low- and high-level cells expressing IFN-gamma in the population. The natural killer (NK) cells and NKT cells were the low-level cells expressing IFN-gamma, and the number of these cells was increased by E2 stimulation. In addition, it was suggested that the enhancing effect of IFN-gamma production by E2 was mediated through estrogen receptor (ER) alpha, and ERbeta agonist stimulated IFN-gamma production. ERs are expressed on plasma membrane as well as in nucleus. The ligand specific to plasma membrane-associated ER (mER) enhanced the IFN-gamma production. In conclusion, our results indicated that E2 up-regulated the IFN-gamma production by mediating ERalpha, ERbeta and mERs.</div>
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