TY - JOUR
T1 - Polycystin-1 regulates amphiregulin expression through CREB and AP1 signalling
T2 - Implications in ADPKD cell proliferation
AU - Aguiari, Gianluca
AU - Bizzarri, Fabiana
AU - Bonon, Anna
AU - Mangolini, Alessandra
AU - Magri, Eros
AU - Pedriali, Massimo
AU - Querzoli, Patrizia
AU - Somlo, Stefan
AU - Harris, Peter C.
AU - Catizone, Luigi
AU - Del Senno, Laura
N1 - Funding Information:
Work supported by grants from CaRiFe, CaRiCe, Italian MIUR COFIN 2008, and Regione Emilia Romagna (Ricerca Regione-Università) 2007–2009. The English was edited by Dr. Anna Forster.
PY - 2012/11
Y1 - 2012/11
N2 - In autosomal dominant polycystic kidney disease (ADPKD), renal cyst development and enlargement, as well as cell growth, are associated with alterations in several pathways, including cAMP and activator protein 1 (AP1) signalling. However, the precise mechanism by which these molecules stimulate cell proliferation is not yet fully understood. We now show by microarray analysis, luciferase assay, mutagenesis, and chromatin immunoprecipitation that CREB and AP1 contribute to increased expression of the amphiregulin gene, which codifies for an epidermal growth factor-like peptide, in ADPKD cystic cells, thereby promoting their cell growth. Increased amphiregulin (AR) expression was associated with abnormal cell proliferation in both PKD1-depleted and -mutated epithelial cells, as well as primary cystic cell lines isolated from ADPKD kidney tissues. Consistently, normal AR expression and proliferation were re-established in cystic cells by the expression of a mouse full-length PC1. Finally, we show that anti-AR antibodies and inhibitors of AP1 are able to reduce cell proliferation in cystic cells by reducing AR expression and EGFR activity. AR can therefore be considered as one of the key activators of the growth of human ADPKD cystic cells and thus a new potential therapeutic target.
AB - In autosomal dominant polycystic kidney disease (ADPKD), renal cyst development and enlargement, as well as cell growth, are associated with alterations in several pathways, including cAMP and activator protein 1 (AP1) signalling. However, the precise mechanism by which these molecules stimulate cell proliferation is not yet fully understood. We now show by microarray analysis, luciferase assay, mutagenesis, and chromatin immunoprecipitation that CREB and AP1 contribute to increased expression of the amphiregulin gene, which codifies for an epidermal growth factor-like peptide, in ADPKD cystic cells, thereby promoting their cell growth. Increased amphiregulin (AR) expression was associated with abnormal cell proliferation in both PKD1-depleted and -mutated epithelial cells, as well as primary cystic cell lines isolated from ADPKD kidney tissues. Consistently, normal AR expression and proliferation were re-established in cystic cells by the expression of a mouse full-length PC1. Finally, we show that anti-AR antibodies and inhibitors of AP1 are able to reduce cell proliferation in cystic cells by reducing AR expression and EGFR activity. AR can therefore be considered as one of the key activators of the growth of human ADPKD cystic cells and thus a new potential therapeutic target.
KW - ADPKD
KW - AP1
KW - Amphiregulin
KW - CREB
KW - Cell proliferation
KW - cAMP
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U2 - 10.1007/s00109-012-0902-3
DO - 10.1007/s00109-012-0902-3
M3 - Article
C2 - 22570239
AN - SCOPUS:84868096068
SN - 0946-2716
VL - 90
SP - 1267
EP - 1282
JO - Journal of Molecular Medicine
JF - Journal of Molecular Medicine
IS - 11
ER -