Takeuchi Kouichi, Koike Kenichi, Kamijo Takehiko, Ishida Shuichi, Nakazawa Yozo, Kurokawa Yumi, Sakashita Kazuo, Kinoshita Tatsuya, Matsuzawa Shigeyuki, Shiohara Masaaki, Yamashita Tetsuji, Nakajima Motowo, Komiyama Atsushi
Department of Pediatrics, Shinshu University School of Medicine, 3-1-1, Asahi, Matsumoto, 390-8621, Japan.
J Leukoc Biol. 2003 Dec;74(6):1026-34. doi: 10.1189/jlb.0602284. Epub 2003 Sep 2.
Stem cell factor (SCF)/c-kit system is critical for human mast cell development. We thus examined the effects of STI571, an inhibitor of the c-kit tyrosine kinase receptor, on the proliferation and function of human mast cells. STI571 at concentrations of 10(-6) M or higher almost completely abolished the SCF-dependent progeny generation from cord blood-derived cultured mast cells through an inhibition of the tyrosine phosphorylation of c-kit. The compound also suppressed the early phase of mast cell development. The extinction of mast cell growth induced by STI571 may be due largely to apoptosis according to the flow cytometric analysis and gel electrophoresis. Two-hour exposure to STI571 that failed to influence the total viable cell number suppressed adhesion of the cells to fibronectin in the presence of SCF without altering the expressions of integrin molecules. Our results may provide a fundamental insight for the clinical application of STI571 in allergic disorders.
干细胞因子(SCF)/c-kit系统对人肥大细胞的发育至关重要。因此,我们研究了c-kit酪氨酸激酶受体抑制剂STI571对人肥大细胞增殖和功能的影响。浓度为10^(-6) M或更高的STI571几乎完全抑制了脐带血来源的培养肥大细胞中SCF依赖性子代细胞的生成,其机制是抑制c-kit的酪氨酸磷酸化。该化合物还抑制了肥大细胞发育的早期阶段。根据流式细胞术分析和凝胶电泳结果,STI571诱导的肥大细胞生长停滞很大程度上可能是由于细胞凋亡。在不影响总活细胞数的情况下,暴露于STI571两小时可抑制细胞在SCF存在下与纤连蛋白的黏附,而不改变整合素分子的表达。我们的结果可能为STI571在过敏性疾病中的临床应用提供重要的见解。