Abstract:
:A protein-tyrosine phosphatase LC-PTP is preferentially expressed in hematopoietic cells and is an early response gene in lymphokine stimulated cells. Here, we found the LC-PTP mRNA induction by IL-2 was markedly inhibited by several tyrosine kinase inhibitors. The induction required both the acidic and serine-rich regions of the IL-2 receptor beta chain (IL-2R beta) in mouse IL-3-dependent pro-B BAF-B03 transfectants. This is strikingly different from the induction of c-myc gene expression, which requires the serine-rich region alone. In addition, overexpression of activated-Lck or -Raf kinases resulted in augmented LC-PTP mRNA expression in myeloid cell line 32D transfectants. Considering the previous findings that the acidic region of the IL-2R beta is responsible for association with Lck and activation of Raf kinase, IL-2-induced expression of LC-PTP mRNA may be primarily transduced through a Lck-Raf mediated signaling pathway.
journal_name
FEBS Lettjournal_title
FEBS lettersauthors
Adachi M,Torigoe T,Sekiya M,Minami Y,Taniguchi T,Hinoda Y,Yachi A,Reed JC,Imai Kdoi
10.1016/0014-5793(95)00952-6subject
Has Abstractpub_date
1995-09-18 00:00:00pages
113-8issue
1eissn
0014-5793issn
1873-3468pii
0014-5793(95)00952-6journal_volume
372pub_type
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