Csk-homologous kinase interacts with SHPS-1 and enhances neurite outgrowth of PC12 cells

Hiroaki Mitsuhashi, Eugene Futai, Noboru Sasagawa, Yukiko Hayashi, Ichizo Nishino, Shoichi Ishiura

研究成果: Article

10 引用 (Scopus)

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SHPS-1 is an immunoglobulin superfamily protein with four immunoreceptor tyrosine-based inhibitory motifs (ITIMs) in its cytoplasmic region. Various neurotrophic factors induce the tyrosine phosphorylation of SHPS-1 and the association of SHPS-1 with the protein tyrosine phosphatase SHP-2. Using a yeast two-hybrid screen, we identified a protein tyrosine kinase, Csk-homologous kinase (CHK), as an SHPS-1-interacting protein. Immunoprecipitation and pull-down assays using glutathione S-transferase (GST) fusion proteins containing the Src homology 2 (SH2) domain of CHK revealed that CHK associates with tyrosine-phosphorylated SHPS-1 via its SH2 domain. HIS3 assay in a yeast two-hybrid system using the tyrosine-to-phenylalanine mutants of SHPS-1 indicated that the first and second ITIMs of SHPS-1 are required to bind CHK. Over-expression of wild-type CHK, but not a kinase-inactive CHK mutant, enhanced the phosphorylation of SHPS-1 and its subsequent association with SHP-2. CHK phosphorylated each of four tyrosines in the cytoplasmic region of SHPS-1 in vitro. Co-expression of SHPS-1 and CHK enhanced neurite outgrowth in PC12 cells. Thus, CHK phosphorylates and associates with SHPS-1 and is involved in neural differentiation via SHP-2 activation.

元の言語English
ページ(範囲)101-112
ページ数12
ジャーナルJournal of Neurochemistry
105
発行部数1
DOI
出版物ステータスPublished - 2008 4 1
外部発表Yes

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience

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