Pleiotrophin stimulates tyrosine phosphorylation of β-adducin through inactivation of the transmembrane receptor protein tyrosine phosphatase β/ζ
- 作者：Harold Pariser ; Pablo Perez-Pinera ; Laura Ezquerra ; Gonzalo Herradon and Thomas F. Deuel
- 关键词：Pleiotrophin ; β ; -Adducin ; Receptor protein tyrosine phosphatase β ; /ζ
- 刊名：Biochemical and Biophysical Research Communications
- 出版年：2005
- 期刊代码：159_0006291x
- 类别：bio
- 出版时间：2005
- 卷：335
- 期：1
- 页码：232-239
- 文件大小：294 K
摘要
Pleiotrophin (PTN the protein, Ptn the gene) signals through a unique mechanism; it inactivates the tyrosine phosphatase activity of its receptor, the transmembrane receptor protein tyrosine phosphatase (RPTP)β/ζ, and increases tyrosine phosphorylation of the substrates of RPTPβ/ζ through the continued activity of a yet to be described protein tyrosine kinase(s) in PTN-stimulated cells. We have now found that the cytoskeletal protein β-adducin interacts with the intracellular domain of RPTPβ/ζ in a yeast two-hybrid system, that β-adducin is a substrate of RPTPβ/ζ, that β-adducin is phosphorylated in tyrosine in cells not stimulated by PTN, and that tyrosine phosphorylation of β-adducin is sharply increased in PTN-stimulated cells, suggesting that β-adducin is a downstream target of and regulated by the PTN/RPTPβ/ζ signaling pathway. β-Catenin was the first downstream target of the PTN/RPTPβ/ζ signaling pathway to be identified; these data thus also suggest that PTN coordinately regulates steady state levels of tyrosine phosphorylation of the important cytoskeletal proteins β-adducin and β-catenin and, through PTN-stimulated tyrosine phosphorylation, β-adducin may contribute to the disruption of cytoskeletal structure, increased plasticity, and loss of homophilic cell–cell adhesion that are the consequences of PTN stimulation of cells and a characteristic feature of different malignant cells with mutations that activate constitutive expression of the endogenous Ptn gene.