Mol. Hum. Reprod. Advance Access originally published online on March 6, 2006
Molecular Human Reproduction 2006 12(4):225-232; doi:10.1093/molehr/gal023
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Involvement of MAPK pathway in TNF-
-induced MMP-9 expression in human trophoblastic cells
Department of Obstetrics and Gynaecology, Maternity, Hormone Laboratory, University of Geneva, Boulevard de la Cluse, Geneva, Switzerland
1 To whom correspondence should be addressed at: Laboratoire dHormonologie, 32 bd de la Cluse, 1211 Genève 14, Switzerland. E-mail: paul.bischof{at}hcuge.ch
The aim of this article was to investigate the signalling pathways involved in metalloproteinase-9 (MMP-9) expression induced by tumour necrosis factor-
(TNF-
) in first-trimester trophoblastic cells. TNF-
-induced MMP-9 expression, secretion and activity were completely blocked by stress-activated protein kinase/jun kinase (SAPK/JNK) and Erk inhibitors (SP600 125 and U0126 respectively) but not by p38 mitogen-activated protein kinase (MAPK) inhibitors (SB203 580 and SB202 190). Stimulation of HIPEC 65 cells with TNF-
caused phosphorylation of JNK and extracellular signal-regulated kinase 1/2 (Erk1/2), with a peak after 20 min of treatment. Transcription factors nuclear factor-
B (NF-
B) and activator protein 1 (AP-1)-binding site were identified as the cis-elements involved in TNF-
activation as determined by electromobility shift assays. TNF-
-induced transactivation of NF-
B was inhibited by U0126, whereas TNF-
-induced transactivation of AP-1 was inhibited by SP600 125. Taken together, these results indicate that in trophoblastic cells, TNF-
probably activates two different pathways leading to MMP-9 expression: (a) Erk1/2 pathway which in turn initiates NF-
B activation and (b) SAPK/JNK pathway that activates AP-1.
Key words:
AP-1/cytotrophoblastic cells/Erk1/2/JNK/MMP-9/NF-
B/TNF-
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