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(-)-表没食子儿茶素没食子酸酯通过抑制成骨细胞中的p44/p42丝裂原活化蛋白激酶途径来抑制前列腺素D2刺激的热休克蛋白27诱导。

(-)-epigallocatechin gallate inhibits prostaglandin D2-stimulated HSP27 induction via suppression of the p44/p42 MAP kinase pathway in osteoblasts.

作者信息

Yamauchi Junichi, Takai Shinji, Matsushima-Nishiwaki Rie, Hanai Yoshiteru, Doi Tomoaki, Kato Hisaaki, Ogura Shinji, Kato Kanefusa, Tokuda Haruhiko, Kozawa Osamu

机构信息

Department of Pharmacology, Gifu University Graduate School of Medicine, Gifu 501-1194, Japan.

出版信息

Prostaglandins Leukot Essent Fatty Acids. 2007 Oct-Nov;77(3-4):173-9. doi: 10.1016/j.plefa.2007.09.001. Epub 2007 Oct 18.

Abstract

We previously reported that prostaglandin D2 (PGD2) stimulates heat shock protein 27 (HSP27) induction through p38 mitogen-activated protein (MAP) kinase, stress-activated protein kinase (SAPK)/c-Jun N-terminal kinase (JNK) and p44/p42 MAP kinase in osteoblast-like MC3T3-E1 cells. In the present study, we investigated whether (-)-epigallocatechin gallate (EGCG), the major polyphenol found in green tea, affects the induction of HSP27 in these cells and the mechanism. EGCG significantly reduced the HSP27 induction stimulated by PGD2 without affecting the levels of HSP70. The PGD2-induced phosphorylation of p38 MAP kinase or SAPK/JNK was not affected by EGCG. On the contrary, EGCG markedly suppressed the PGD2-induced phosphorylation of p44/p42 MAP kinase and MEK1/2. However, the PGD2-induced phosphorylation of Raf-1 was not inhibited by EGCG. These results strongly suggest that EGCG suppresses the PGD2-stimulated induction of HSP27 at the point between Raf-1 and MEK1/2 in osteoblasts.

摘要

我们之前报道过,前列腺素D2(PGD2)通过p38丝裂原活化蛋白(MAP)激酶、应激激活蛋白激酶(SAPK)/c-Jun氨基末端激酶(JNK)和p44/p42 MAP激酶,刺激成骨样MC3T3-E1细胞中热休克蛋白27(HSP27)的诱导。在本研究中,我们调查了绿茶中主要的多酚成分(-)-表没食子儿茶素没食子酸酯(EGCG)是否影响这些细胞中HSP27的诱导及其机制。EGCG显著降低了PGD2刺激的HSP27诱导,而不影响HSP70的水平。EGCG不影响PGD2诱导的p38 MAP激酶或SAPK/JNK的磷酸化。相反,EGCG显著抑制了PGD2诱导的p44/p42 MAP激酶和MEK1/2的磷酸化。然而,EGCG不抑制PGD2诱导的Raf-1的磷酸化。这些结果强烈表明,EGCG在成骨细胞中Raf-1和MEK1/2之间的位点抑制PGD2刺激的HSP27诱导。

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