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丝裂原活化蛋白激酶激酶的激活对于PC12细胞分化和NIH 3T3细胞转化而言是必要且充分的。

Activation of MAP kinase kinase is necessary and sufficient for PC12 differentiation and for transformation of NIH 3T3 cells.

作者信息

Cowley S, Paterson H, Kemp P, Marshall C J

机构信息

Section of Cell and Molecular Biology, Chester Beatty Laboratories, Institute of Cancer Research, London, England.

出版信息

Cell. 1994 Jun 17;77(6):841-52. doi: 10.1016/0092-8674(94)90133-3.

Abstract

The MAP kinase pathway is activated by a wide variety of external signals leading to cell proliferation or differentiation. However, it is not clear whether activation of this pathway is required for cellular responses or whether it is only one branch point in signal transduction. To investigate these questions, we generated constitutively activated and interfering mutants of MAP kinase kinase 1. The activated mutants stimulated PC12 cell neuronal differentiation and transformed NIH 3T3 cells. The interfering mutants inhibited growth factor-induced PC12 differentiation, growth factor stimulation of proliferation, and reverted v-src- and ras-transformed cells. These results therefore show that, depending on cellular context, activation of MAP kinase kinase is necessary and sufficient for cell differentiation or proliferation.

摘要

丝裂原活化蛋白激酶(MAP激酶)信号通路可被多种外部信号激活,从而导致细胞增殖或分化。然而,目前尚不清楚该信号通路的激活对于细胞反应是否必需,或者它是否仅仅是信号转导中的一个分支点。为了研究这些问题,我们构建了组成型激活和干扰性的丝裂原活化蛋白激酶激酶1(MAP激酶激酶1)突变体。激活型突变体刺激了PC12细胞的神经元分化并使NIH 3T3细胞发生转化。干扰性突变体抑制了生长因子诱导的PC12细胞分化、生长因子对增殖的刺激,并使v-src和ras转化的细胞回复正常。因此,这些结果表明,根据细胞环境的不同,丝裂原活化蛋白激酶激酶的激活对于细胞分化或增殖而言是必要且充分的。

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