SHP2 regulates IL-2 induced MAPK activation, but not Stat3 or Stat5 tyrosine phosphorylation, in cutaneous T cell lymphoma cells

被引:12
作者
Brockdorff, JL
Woetmann, A
Mustelin, T
Kaltoft, K
Zhang, Q
Wasik, MA
Röpke, C
Odum, N
机构
[1] Univ Copenhagen, Inst Med Microbiol & Immunol, Panum Inst, DK-2200 Copenhagen N, Denmark
[2] Burnham Inst, La Jolla, CA 92037 USA
[3] Univ Aarhus, Inst Human Genet, Aarhus, Denmark
[4] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[5] Sect A, Inst Med Anat, Copenhagen, Denmark
关键词
CTCL; IL-2; MAPK; SHP2; Stat;
D O I
10.1006/cyto.2002.1986
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
The phosphotyrosine phosphatase SHP2 has been suggested to regulate activation of MAPK, Stat3, and Stat5 in several experimental models. In this study we investigated the role of SHP2 in IL-2 induced activation of MAPK and the Stat proteins using the human CTCL cell line MyLa2059 derived from a cutaneous T cell lymphoma (CTCL). For this purpose, MyLa2059 cells were stably transfected with wild-type SHP2 or inactive SHP2. The cells transfected with inactive SHP2 showed reduced MAPK activation upon IL-2 stimulation, suggesting that SHP2 upregulates IL-2 induced MAPK activation in T cells. However, the constitutive tyrosine phosphorylation of Stat3 as well as IL-2 induced Stat5 tyrosine phosphorylation and DNA binding were unaffected by the stably transfected wild-type SHP2 as well as the inactive SHP2. In conclusion, we show for the first time that SHP2 positively regulates IL-2 induced MAPK activation in malignant T cells. Furthermore, the results indicate that SHP2 may not be involved in the activation of Stat3 or Stat5 in CTCL cells. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:141 / 147
页数:7
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