Protein-tyrosine phosphatase PTPεC inhibits Jak-STAT signaling and differentiation induced by interleukin-6 and leukemia inhibitory factor in M1 leukemia cells

被引:0
|
作者
Tanuma, N [1 ]
Nakamura, K [1 ]
Shima, H [1 ]
Kikuchi, K [1 ]
机构
[1] Hokkaido Univ, Inst Med Genet, Div Biochem Oncol & Immunol, Kita Ku, Sapporo, Hokkaido 0600815, Japan
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中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We engineered and expressed bath a wild-type and mutant cytosolic isoform of PTP epsilon (PTP epsilon C) in murine M1 leukemic cells, which can be induced to growth arrest and monocytic differentiation by interleukin (IL)-6 and leukemia inhibitory factor (LIF). Forced expression of PTP epsilon C inhibited IL-6- and LIF-induced monocytic differentiation and apoptosis in M1 cells, whereas expression of PTP epsilon M, a transmembrane isoform of PTP epsilon, did not. PTP epsilon C expression resulted in lower levels of IL-6-induced tyrosine phosphorylation of Jak1, Tyk2, gp130, and Stat3 compared with parent cells. In MI transfectants expressing an inactive mutant of PTP epsilon C, both tyrosine phosphorylation and apoptosis induced by IL-6- and LIF were potentiated rather than inhibited. These results suggest an important role for PTP epsilon C in negative regulation of IL-6- and LIF-induced Jak-STAT signaling.
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页码:28216 / 28221
页数:6
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