论文部分内容阅读
目的:确定与细胞内蛋白质酪氨酸磷酸化相关的激酶。方法:用粒-巨噬系集落刺激因子(GM-CSF)和红细胞生成素(Epo)依赖细胞株UT-7以及Epo依赖细胞株UT-7/Epo进行酪氨酸磷酸化的研究。结果:当GM-CSF或Epo刺激其生长依赖细胞时可快速诱导分子量为145000,130000,80000和40000等多种蛋白质酪氨酸磷酸化。鉴定了分子量为130000酪氨酸磷酸化的蛋白质为JAK2,一种非受体型酪氨酸激酶。同时,GM-CSF或Epo刺激亦可激活JAK2激酶活性。酪氨酸磷酸化和激活JAK2只发生在GM-CSF或Epo生长依赖细胞。结论:JAK2信号传导途径在GM-CSF和Epo诱导的细胞增殖中起重要作用。
Purpose: To identify kinases associated with intracellular protein tyrosine phosphorylation. Methods: The tyrosine phosphorylation of GM-CSF and erythropoietin-dependent cell line UT-7 and Epo-dependent cell line UT-7 / Epo were studied. Results: When GM-CSF or Epo stimulated their growth-dependent cells, they could rapidly induce a variety of protein tyrosine phosphorylation with molecular weights of 145,000, 130,000, 80,000 and 40,000. A protein of tyrosine phosphorylation at 130000 was identified as JAK2, a non-receptor tyrosine kinase. In the meantime, stimulation with GM-CSF or Epo also activates JAK2 kinase activity. Tyrosine phosphorylation and activation JAK2 occurs only in GM-CSF or Epo growth-dependent cells. Conclusion: The JAK2 signaling pathway plays an important role in GM-CSF and Epo-induced cell proliferation.