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苹果原花青素通过一种不依赖脂筏的机制激活人结肠腺癌细胞中的凋亡信号通路。

Apple procyanidins activate apoptotic signaling pathway in human colon adenocarcinoma cells by a lipid-raft independent mechanism.

作者信息

Maldonado-Celis Maria E, Bousserouel Souad, Gossé Francine, Lobstein Annelise, Raul Francis

机构信息

Université de Strasbourg Unit 4438, Faculté de Médecine, 67000 Strasbourg, France.

出版信息

Biochem Biophys Res Commun. 2009 Oct 16;388(2):372-6. doi: 10.1016/j.bbrc.2009.08.016. Epub 2009 Aug 8.

DOI:10.1016/j.bbrc.2009.08.016
PMID:19666002
Abstract

Flavonoids are polyphenolic compounds able to favour cholesterol-lipid-raft formation and control cell signaling pathways by targeting receptors at the cell surface. Procyanidins (Pcy) are oligomeric and polymeric flavonoids formed by catechins and epicatechins monomers trigger apoptosis by activating TRAIL-death receptors in human colon adenocarcinoma SW480 cells. Here, we investigated whether the apoptotic process triggered by apple procyanidins involving the up-regulation of TRAIL-death receptors DR4/DR5 at the cell surface was dependent on cell membrane lipid-raft formation. We report that Pcy-induced apoptosis was enhanced in presence of nystatin, a cholesterol-sequestering compound inhibiting lipid-raft formation, without changing DR4/DR5 receptor expression. Treatment of SW480 cells with TRAIL caused a 3.5-fold increased level of caveolin together with a 2- to 2.5-fold increased amount of DR4/DR5 proteins in lipid rafts. Pcy-treatment did not induce any alteration in the expression of DR4/DR5 proteins as well as of caveolin present in lipid-raft fractions. Pcy induced an activation of TRAIL-death receptor-mediated apoptosis by a mechanism independent of lipid-raft formation. These results highlight the potential of Pcy as a direct activator of TRAIL-death receptors in cell membrane even in the absence of lipid rafts.

摘要

黄酮类化合物是多酚类化合物,能够促进胆固醇 - 脂筏的形成,并通过靶向细胞表面的受体来控制细胞信号通路。原花青素(Pcy)是由儿茶素和表儿茶素单体形成的寡聚和聚合黄酮类化合物,通过激活人结肠腺癌SW480细胞中的TRAIL死亡受体来触发细胞凋亡。在这里,我们研究了苹果原花青素触发的凋亡过程,该过程涉及细胞表面TRAIL死亡受体DR4/DR5的上调,是否依赖于细胞膜脂筏的形成。我们报告说,在制霉菌素(一种抑制脂筏形成的胆固醇螯合化合物)存在的情况下,Pcy诱导的细胞凋亡增强,而DR4/DR5受体表达没有改变。用TRAIL处理SW480细胞导致脂筏中小窝蛋白水平增加3.5倍,同时DR4/DR5蛋白量增加2至2.5倍。Pcy处理不会诱导脂筏组分中存在的DR4/DR5蛋白以及小窝蛋白的表达发生任何改变。Pcy通过一种独立于脂筏形成的机制诱导TRAIL死亡受体介导的细胞凋亡激活。这些结果突出了Pcy作为细胞膜中TRAIL死亡受体直接激活剂的潜力,即使在没有脂筏的情况下也是如此。

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