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MAP kinase activation by interleukin-9 in lymphoid and mast cell lines

机译:白细胞介素9在淋巴和肥大细胞系中激活MAP激酶

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摘要

Interleukin-9 (IL-9) stimulates the proliferation of mast cells and lymphocytes. In the present study, we showed that IL-9 induced a transient phosphorylation of MEK, ERK2 and p90/RSK in murine lymphoid and mast cell lines. ERK2 in vitro kinase activity was also increased upon IL-9 stimulation. Similar results were obtained with IL-4, which had not been previously reported to activate these kinases in hematopoietic cells. Analysis of IL-9 receptor mutants showed that activation of the pathway was correlated with proliferation and with phosphorylation of the adaptor protein SHC, but not IRS2 or GAB2. The MEK inhibitor PD98059 reduced the mitogenic response to IL-4 and IL-9. In addition, expression of a dominant-negative RAS variant blocked ERK phosphorylation and significantly decreased Ba/F3 cell growth in the presence of IL-9, but did not affect expression of pim-1, a STAT target gene. In summary, these results indicate that IL-9 can transiently activate the mitogen-activated protein kinase pathway, which contributes to growth stimulation of hematopoietic cell lines.
机译:白介素9(IL-9)刺激肥大细胞和淋巴细胞的增殖。在本研究中,我们显示IL-9在鼠淋巴和肥大细胞系中诱导了MEK,ERK2和p90 / RSK的瞬时磷酸化。 IL-9刺激后,ERK2体外激酶活性也增加。 IL-4获得了相似的结果,以前尚未报道过可以激活造血细胞中的这些激酶。对IL-9受体突变体的分析表明,该途径的激活与衔接蛋白SHC(而非IRS2或GAB2)的增殖和磷酸化相关。 MEK抑制剂PD98059降低了对IL-4和IL-9的促有丝分裂反应。此外,在IL-9存在下,显性阴性RAS变体的表达可阻断ERK磷酸化并显着降低Ba / F3细胞的生长,但不会影响STAT目标基因pim-1的表达。总之,这些结果表明IL-9可以瞬时激活促分裂原活化的蛋白激酶途径,这有助于造血细胞系的生长刺激。

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