A Novel Interaction between Pyk2 and MAP4K4 Is Integrated with Glioma Cell Migration. (15th September 2013)

• Record Type: Journal Article
• Authors: Loftus, Joseph C.; Yang, Zhongbo; Kloss, Jean; Dhruv, Harshil; Tran, Nhan L.; Riggs, Daniel L.
• Other Names: Gaestel Matthias Academic Editor.
• Is Part Of: Journal of signal transduction. Volume 2013(2013)
• Publication Date: 2013-09-15
• Subjects: Cellular signal transduction -- Periodicals; Signal Transduction; Cellular signal transduction; Periodical; Periodicals; Electronic journals; 616.0277
• DOI: 10.1155/2013/956580
• Languages: English
• ISSNs: 2090-1739

Abstract

Abstract : Glioma cell migration correlates with Pyk2 activity, but the intrinsic mechanism that regulates the activity of Pyk2 is not fully understood. Previous studies have supported a role for the N-terminal FERM domain in the regulation of Pyk2 activity as mutations in the FERM domain inhibit Pyk2 phosphorylation. To search for novel protein-protein interactions mediated by the Pyk2 FERM domain, we utilized a yeast two-hybrid genetic selection to identify the mammalian Ste20 homolog MAP4K4 as a binding partner for the Pyk2 FERM domain. MAP4K4 coimmunoprecipitated with Pyk2 and was a substrate for Pyk2 but did not coimmunoprecipitate with the closely related focal adhesion kinase FAK. Knockdown of MAP4K4 expression inhibited glioma cell migration and effectively blocked Pyk2 stimulation of glioma cell. Increased expression of MAP4K4 stimulated glioma cell migration; however, this stimulation was blocked by knockdown of Pyk2 expression. These data support that the interaction of MAP4K4 and Pyk2 is integrated with glioma cell migration and suggest that inhibition of this interaction may represent a potential therapeutic strategy to limit glioblastoma tumor dispersion.