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多囊蛋白-1 通过 CREB 和 AP1 信号通路调节 Amphiregulin 的表达:在 ADPKD 细胞增殖中的意义。

Polycystin-1 regulates amphiregulin expression through CREB and AP1 signalling: implications in ADPKD cell proliferation.

机构信息

Department of Biochemistry and Molecular Biology, University of Ferrara, via Fossato di Mortara, 74, 44121 Ferrara, Italy.

出版信息

J Mol Med (Berl). 2012 Nov;90(11):1267-82. doi: 10.1007/s00109-012-0902-3. Epub 2012 May 9.

Abstract

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.

摘要

在常染色体显性多囊肾病(ADPKD)中,肾脏囊肿的形成和增大以及细胞生长与几种途径的改变有关,包括 cAMP 和激活蛋白 1(AP1)信号通路。然而,这些分子刺激细胞增殖的确切机制尚未完全阐明。我们现在通过微阵列分析、荧光素酶测定、突变和染色质免疫沉淀表明,CREB 和 AP1 有助于增加 amphiregulin(编码表皮生长因子样肽)基因在 ADPKD 囊性细胞中的表达,从而促进其细胞生长。在 PKD1 耗尽和突变的上皮细胞以及从 ADPKD 肾脏组织中分离出的原发性囊性细胞系中,增加的 amphiregulin(AR)表达与异常细胞增殖相关。一致地,通过表达全长的 PC1,在囊性细胞中可以重新建立正常的 AR 表达和增殖。最后,我们表明,抗 AR 抗体和 AP1 抑制剂通过降低 AR 表达和 EGFR 活性能够减少囊性细胞的增殖。因此,AR 可以被认为是人类 ADPKD 囊性细胞生长的关键激活剂之一,也是一个新的潜在治疗靶点。

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