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多囊肾病1基因产物介导转录因子AP-1的蛋白激酶Cα依赖性和c-Jun氨基末端激酶依赖性激活。

The polycystic kidney disease 1 gene product mediates protein kinase C alpha-dependent and c-Jun N-terminal kinase-dependent activation of the transcription factor AP-1.

作者信息

Arnould T, Kim E, Tsiokas L, Jochimsen F, Grüning W, Chang J D, Walz G

机构信息

Renal Division, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA.

出版信息

J Biol Chem. 1998 Mar 13;273(11):6013-8. doi: 10.1074/jbc.273.11.6013.

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is a common hereditary disorder that accounts for 8-10% of end stage renal disease. PKD1, one of two recently isolated ADPKD gene products, has been implicated in cell-cell and cell-matrix interactions. However, the signaling pathway of PKD1 remains undefined. We found that the C-terminal 226 amino acids of PKD1 transactivate an AP-1 promoter construct in human embryonic kidney cells (293T). PKD1-induced transcription is specific for AP-1; promoter constructs containing cAMP response element-binding protein, c-Fos, c-Myc, or NFkappaB-binding sites are unaffected by PKD1. In vitro kinase assays revealed that PKD1 triggers the activation of c-Jun N-terminal kinase (JNK), but not of mitogen-activated protein kinases p38 or p44. Dominant-negative Rac-1 and Cdc42 mutations abrogated PKD1-mediated JNK and AP-1 activation, suggesting a critical role for small GTP-binding proteins in PKD1-mediated signaling. Several protein kinase C (PKC) inhibitors decreased PKD1-mediated AP-1 activation. Conversely, expression of the C-terminal domain of PKD1 increased PKC activity in 293T cells. A dominant-negative PKC alpha, but not a dominant-negative PKC beta or delta, abrogated PKD1-mediated AP-1 activation. These findings indicate that small GTP-binding proteins and PKC alpha mediate PKD1-induced JNK/AP-1 activation, together comprising a signaling cascade that may regulate renal tubulogenesis.

摘要

常染色体显性遗传性多囊肾病(ADPKD)是一种常见的遗传性疾病,占终末期肾病的8 - 10%。PKD1是最近分离出的两种ADPKD基因产物之一,与细胞间和细胞与基质的相互作用有关。然而,PKD1的信号通路仍不明确。我们发现PKD1的C末端226个氨基酸在人胚肾细胞(293T)中可激活AP - 1启动子构建体。PKD1诱导的转录对AP - 1具有特异性;含有环磷酸腺苷反应元件结合蛋白、c - Fos、c - Myc或核因子κB结合位点的启动子构建体不受PKD1影响。体外激酶分析显示,PKD1可触发c - Jun氨基末端激酶(JNK)的激活,但不影响丝裂原活化蛋白激酶p38或p44。显性负性Rac - 1和Cdc42突变消除了PKD1介导的JNK和AP - 1激活,表明小GTP结合蛋白在PKD1介导的信号传导中起关键作用。几种蛋白激酶C(PKC)抑制剂降低了PKD1介导的AP - 1激活。相反,PKD1 C末端结构域的表达增加了293T细胞中的PKC活性。显性负性PKCα可消除PKD1介导的AP - 1激活,而显性负性PKCβ或δ则无此作用。这些发现表明,小GTP结合蛋白和PKCα介导PKD1诱导的JNK/AP - 1激活,共同构成一个可能调节肾小管生成的信号级联反应。

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