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灰树花中的溶血磷脂酰乙醇胺通过激活丝裂原活化蛋白激酶作为神经营养激活剂。

Lysophosphatidylethanolamine in Grifola frondosa as a neurotrophic activator via activation of MAPK.

作者信息

Nishina Atsuyoshi, Kimura Hirokazu, Sekiguchi Akihiro, Fukumoto Ryo-hei, Nakajima Satoshi, Furukawa Shoei

机构信息

Gunma Industrial Technology Center, 884-1 Kamesato, Maebashi, Gunma 379-2147, Japan.

出版信息

J Lipid Res. 2006 Jul;47(7):1434-43. doi: 10.1194/jlr.M600045-JLR200. Epub 2006 Apr 13.

DOI:10.1194/jlr.M600045-JLR200
PMID:16614393
Abstract

We found that Grifola frondosa extracts induced the activation of mitogen-activated protein kinase (MAPK) in cultured PC12 cells, a line of rat pheochromocytoma cells. The active substance was isolated by a few chromatographic steps, including high-performance liquid chromatography, and was identified to be lysophosphatidylethanolamine (LPE) from various structural analyses. LPE from G. frondosa (GLPE) was confirmed to induce the activation of MAPK of cultured PC12 cells and was found to suppress cell condensation and DNA ladder generation evoked by serum deprivation, suggesting that the GLPE had antiapoptotic effects. Moreover, GLPE caused morphological changes in and upregulation of neurofilament M expression of PC12 cells, demonstrating that the GLPE could induce neuronal differentiation of these cells. The activation of MAPK by GLPE was suppressed by AG1478, an antagonist of epidermal growth factor receptor (EGFR), and by U0126, an inhibitor of MAPK kinase (MEK1/2), but not by K252a, an inhibitor of TrkA, or by pertussis toxin. These results demonstrate that GLPE induced the MAPK cascade [EGFR-MEK1/2-extracellular signal-regulated protein kinases (ERK1/2)] of PC12 cells, the activation of which induced neuronal differentiation and suppressed serum deprivation-induced apoptosis. This study has clarified for the first time the involvement of the MAPK signal cascade in LPE actions.

摘要

我们发现,灰树花提取物可诱导培养的PC12细胞(一种大鼠嗜铬细胞瘤细胞系)中丝裂原活化蛋白激酶(MAPK)的激活。通过包括高效液相色谱在内的几个色谱步骤分离出活性物质,并通过各种结构分析鉴定为溶血磷脂酰乙醇胺(LPE)。来自灰树花的LPE(GLPE)被证实可诱导培养的PC12细胞中MAPK的激活,并被发现可抑制血清剥夺引起的细胞浓缩和DNA梯带产生,这表明GLPE具有抗凋亡作用。此外,GLPE引起PC12细胞形态变化并上调神经丝M的表达,表明GLPE可诱导这些细胞的神经元分化。GLPE对MAPK的激活被表皮生长因子受体(EGFR)拮抗剂AG1478和MAPK激酶(MEK1/2)抑制剂U0126抑制,但未被TrkA抑制剂K252a或百日咳毒素抑制。这些结果表明,GLPE诱导了PC12细胞的MAPK级联反应[EGFR-MEK1/2-细胞外信号调节蛋白激酶(ERK1/2)],其激活诱导了神经元分化并抑制了血清剥夺诱导的细胞凋亡。本研究首次阐明了MAPK信号级联在LPE作用中的参与情况。

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