Differential inhibition of Smad6 and Smad7 on bone morphogenetic protein- and activin-mediated growth arrest and apoptosis in B cells

被引:195
作者
Ishisaki, A
Yamato, K
Hashimoto, S
Nakao, A
Tamaki, K
Nonaka, K
ten Dijke, P
Sugino, H
Nishihara, T
机构
[1] Nstl Inst Infect Dis, Dept Oral Sci, Shinjuku Ku, Tokyo 1628640, Japan
[2] Tokyo Med & Dent Univ, Fac Dent, Dept Mol Cellular Oncol Microbiol, Bunkyo Ku, Tokyo 1138549, Japan
[3] Tokyo Med & Dent Univ, Fac Dent, Dept Oral & Maxillofacial Surg 1, Bunkyo Ku, Tokyo 1138549, Japan
[4] Chiba Univ, Sch Med, Dept Med, Chuo Ku, Chiba 2600856, Japan
[5] Univ Tokushima, Inst Enzyme Res, Tokushima 770, Japan
[6] Biomed Ctr, Ludwig Inst Canc Res, S-75124 Uppsala, Sweden
关键词
D O I
10.1074/jbc.274.19.13637
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
Smad6 and Smad7 prevent ligand-induced activation of signal-transducing Smad proteins in the transforming growth factor-p family. Here we demonstrate that both Smad6 and Smad7 are human bone morphogenetic protein-2 (hBMP-2)-inducible antagonists of hBMP-2-induced growth arrest and apoptosis in mouse B cell hybridoma HS-72 cells. Moreover, we confirmed that the ectopic expressions of Smad6 and Smad7 inhibited the hBMP-2-induced Smad1/Smad5 phosphorylation. We previously reported that Smad7 is an activin A-inducible antagonist of activin A-induced growth arrest and apoptosis in HS-72 cells. Interestingly, although mRNA expression of Smad6 was induced by activin A in HS-72 cells, Smad6 showed no antagonistic effect on activin A-induced growth arrest and apoptosis, Moreover, we found that the ectopic expression of Smad7, but not Smad6, inhibited the activin A-induced Smad2 phosphorylation in HS-72 cells. Thus, Smad6 and Smad7 exhibit differential inhibitory effects in bone morphogenetic protein-2- and activin A-mediated signaling in B lineage cells.
引用
收藏
页码:13637 / 13642
页数:6
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