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1.
Endocrinology ; 141(12): 4457-65, 2000 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-11108255

RESUMO

Bacterial lipopolysaccharide (LPS) activates the immune system and induces increases in peripheral cytokines, which, in turn, affect the endocrine system. In particular, LPS-induced cytokines stimulate the hypothalamic-pituitary-adrenal axis to increase levels of antiinflammatory-acting glucocorticoids. In the present work, we show that LPS directly stimulates interleukin (IL)-6 release by mouse pituitary folliculostellate (FS) TtT/GF tumor cells and FS cells of mouse pituitary cell cultures. The stimulatory effect of LPS was strongly enhanced in the presence of serum, suggesting that LPS is only fully active as a complex with LPS-binding protein (LBP). Both TtT/GF cells and mouse pituitaries expressed CD14, which binds the LPS/LBP complex, and Toll-like receptor type 4, which induces LPS signals. LPS increased phospoinositol turnover in TtT/GF cells and induced phosphorylation of p38alpha mitogen-activated protein kinase and the inhibitor (IkappaB) of nuclear factor-kappa B. Nuclear factor-kappa B was activated by LPS in TtT/GF cells. Functional studies demonstrated that My4 (an antibody blocking the interaction between LPS/LBP and CD14), SB203580, (a specific inhibitor of p38alpha mitogen-activated protein kinase phosphorylation), dexamethasone, and the messenger RNA translation inhibitor cycloheximide all inhibited LPS-induced IL-6 production by TtT/GF cells and mouse pituitary FS cells. LPS-induced intrapituitary IL-6 may modulate the function of anterior pituitary cells during bacterial infection/inflammation.


Assuntos
Proteínas de Fase Aguda , Interleucina-6/biossíntese , Lipopolissacarídeos/farmacologia , Glicoproteínas de Membrana , Proteínas Quinases Ativadas por Mitógeno/metabolismo , NF-kappa B/metabolismo , Adeno-Hipófise/metabolismo , Animais , Anticorpos/farmacologia , Proteínas de Transporte/metabolismo , Proteínas de Transporte/farmacologia , Linhagem Celular , Células Cultivadas , AMP Cíclico/metabolismo , Cicloeximida/farmacologia , Dexametasona/farmacologia , Glucocorticoides/farmacologia , Imidazóis/farmacologia , Fosfatos de Inositol/metabolismo , Receptores de Lipopolissacarídeos/metabolismo , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Fosfatidilinositóis/metabolismo , Fosforilação , Piridinas/farmacologia , Transdução de Sinais
2.
Endocrinology ; 141(5): 1746-53, 2000 May.
Artigo em Inglês | MEDLINE | ID: mdl-10803585

RESUMO

Two of the most potent cytokines regulating anterior pituitary cell function are leukemia inhibitory factor and interleukin-6 (IL-6), which belong to the cytokine receptor family using the common gp130 signal transducer. We studied the actions of two other members of this family, IL-11 and ciliary neurotropic factor (CNTF), on folliculostellate (FS) cells (TtT/GF cell line) and lactosomatotropic cells (GH3 cell line). The messenger RNA (mRNA) for the alpha-chain specific for the IL-11 receptor (1.7 kb) and CNTF receptor (2 kb) are expressed on both cell types. In addition, we detected CNTF receptor mRNA in normal rat anterior pituitary cells. IL-11 (1.25-5 nM) dose dependently stimulated the proliferation of FS cells. CNTF, at doses from 0.4-2 nM, also significantly stimulated the growth of these cells. In addition, both cytokines significantly stimulated proliferation of lactosomatotropic GH3 cells, and CNTF stimulated hormone production (GH and PRL) at 24 h by these cells. At 16-72 h, IL-11 stimulates the secretion of the angiogenic factor vascular endothelial growth factor by FS cells. In addition, both GH3 and FS cells express CNTF mRNA. These data suggest that IL-11 and CNTF may act as growth and regulatory factors in anterior pituitary cells.


Assuntos
Fator Neurotrófico Ciliar/fisiologia , Interleucina-11/fisiologia , Lactação/fisiologia , Adeno-Hipófise/fisiologia , Receptor do Fator Neutrófico Ciliar/biossíntese , Receptores de Interleucina/biossíntese , Animais , Divisão Celular , Linhagem Celular , Fatores de Crescimento Endotelial/metabolismo , Feminino , Subunidade alfa de Receptor de Interleucina-11 , Linfocinas/metabolismo , Masculino , Adeno-Hipófise/citologia , Ratos , Ratos Sprague-Dawley , Receptor do Fator Neutrófico Ciliar/genética , Receptores de Interleucina/genética , Receptores de Interleucina-11 , Proteínas Recombinantes/farmacologia , Fator A de Crescimento do Endotélio Vascular , Fatores de Crescimento do Endotélio Vascular
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