| Literature DB >> 20360400 |
Tatsuaki Tsuruyama1, Yukiko Imai, Haruya Takeuchi, Takuya Hiratsuka, Yasuhiro Maruyama, Kazuya Kanaya, Richard Kaszynski, Guang Jin, Tomoko Okuno, Munetaka Ozeki, Takuro Nakamura, Tetsuya Takakuwa, Toshiaki Manabe, Keiji Tamaki, Hiroshi Hiai.
Abstract
IL-7R, FLT3, and CD43 are surface antigens expressed during the transition from pro-B to pre-B cells in BM. To understand interactions between their signaling pathways, we analyzed spontaneous mouse B-LBLs with dual MLV integration into Stat5a and Fiz1 or Stat5a and Hipk2. MLV integration resulted in up-regulation of these genes in lymphoma cells compared with normal pro-B cells from the BM. In lymphomas with both integrations into Stat5a and Fiz1, increases in phosphorylated STAT5A and expression of c-Myc, a target gene of STAT5A, were observed following stimulation of the FLT3. Clones with the dual integrations grew faster in IL-7 and FLT3L-supplemented medium than clones with Stat5a integration alone. On the other hand, in lymphomas with integrations into Stat5a and Hipk2, increases in phosphorylated STAT5A and expression of c-Myc were observed following cross-linking of CD43. In conclusion, FLT3 and CD43 signaling pathways involve STAT5A via Fiz1 and Hipk2 in B-LBLs. Identification of the dual MLV integration sites in B-LBLs, therefore, will provide an excellent tool for identification of the signaling pathways in B-LBLs.Entities:
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Year: 2010 PMID: 20360400 DOI: 10.1189/jlb.1109748
Source DB: PubMed Journal: J Leukoc Biol ISSN: 0741-5400 Impact factor: 4.962