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Relaxin induces matrix-metalloproteinases-9 and-13 via RXFP1: Induction of MMP-9 involves the PI3K, ERK, Akt and PKC-ζ pathways
被引:55
作者:
Ahmad, Nisar
[1
]
Wang, Wei
[1
]
Nair, Remi
[1
]
Kapila, Sunil
[1
]
机构:
[1] Univ Michigan, Ann Arbor, MI 48109 USA
关键词:
Relaxin receptors;
Synovial joint fibrochondrocytes;
Matrix metalloproteinases;
ERK;
Akt;
Transcription factors;
FAMILY PEPTIDE RECEPTORS;
NF-KAPPA-B;
GENE-KNOCKOUT MOUSE;
RAT PUBIC SYMPHYSIS;
KINASE-C-ZETA;
SIGNALING PATHWAYS;
IN-VITRO;
CYCLIC ADENOSINE-3';
5'-MONOPHOSPHATE;
MATRIX METALLOPROTEINASES;
FIBROCARTILAGINOUS CELLS;
D O I:
10.1016/j.mce.2012.07.006
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
We determined the precise role of relaxin family peptide (RXFP) receptors-1 and -2 in the regulation of MMP-9 and -13 by relaxin, and delineated the signaling cascade that contributes to relaxin's modulation of MMP-9 in fibrocartilaginous cells. Relaxin treatment of cells in which RXFP1 was silenced resulted in diminished induction of MMP-9 and -13 by relaxin, whereas overexpression of RXFP1 potentiated the relaxin-induced expression of these proteinases. Suppression or overexpression of RXFP2 resulted in no changes in the relaxin-induced MMP-9 and -13. Studies using chemical inhibitors and siRNAs to signaling molecules showed that PI3K, Akt, ERK and PKC-zeta and the transcription factors EIk-1, c-fos and, to a lesser extent, NF-kappa B are involved in relaxin's induction of MMP-9. Our findings provide the first characterization of signaling cascade involved in the regulation of any MMP by relaxin and offer mechanistic insights on how relaxin likely mediates extracellular matrix turnover. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
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页码:46 / 61
页数:16
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