首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >The cyclopentenone 15-deoxy-Δ1214-prostaglandin J2 binds to and activates H-Ras
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The cyclopentenone 15-deoxy-Δ1214-prostaglandin J2 binds to and activates H-Ras

机译:环戊烯酮15-脱氧-Δ1214-前列腺素J2结合并激活H-Ras

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摘要

The cyclopentenone 15-deoxy-Δ12,14-prostaglandin J2 (15d-PGJ2) induces cell proliferation and mitogen-activated protein kinase activation. Here, we describe that these effects are mediated by 15d-PGJ2-elicited H-Ras activation. We demonstrate that this pathway is specific for H-Ras through the formation of a covalent adduct of 15d-PGJ2 with Cys-184 of H-Ras, but not with N-Ras or K-Ras. Mutation of C184 inhibited H-Ras modification and activation by 15d-PGJ2, whereas serum-elicited stimulation was not affected. These results describe a mechanism for the activation of the Ras signaling pathway, which results from the chemical modification of H-Ras by formation of a covalent adduct with cyclopentenone prostaglandins.
机译:环戊烯酮15-脱氧-Δ 12,14 -前列腺素J2(15d-PGJ2)诱导细胞增殖和丝裂原活化的蛋白激酶活化。在这里,我们描述了这些作用是由15d-PGJ2引起的H-Ras激活介导的。我们证明该途径是特定于H-Ras的,它通过与H-Ras的Cys-184形成15d-PGJ2的共价加合物形成,而不是与N-Ras或K-Ras形成。 C184的突变通过15d-PGJ2抑制H-Ras修饰和激活,而血清引起的刺激不受影响。这些结果描述了激活Ras信号通路的机制,该机制是通过与环戊烯酮前列腺素形成共价加合物对H-Ras进行化学修饰而产生的。

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