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不饱和脂肪酸诱导的α-乳白蛋白细胞毒性聚集体可诱导肿瘤细胞凋亡。

Cytotoxic aggregates of alpha-lactalbumin induced by unsaturated fatty acid induce apoptosis in tumor cells.

作者信息

Zhang Min, Yang Fang, Yang Fang, Chen Jie, Zheng Cong-Yi, Liang Yi

机构信息

State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China.

出版信息

Chem Biol Interact. 2009 Jul 15;180(2):131-42. doi: 10.1016/j.cbi.2009.03.019. Epub 2009 Apr 5.

Abstract

The effects of three fatty acids on cytotoxic aggregate formation of Ca(2+)-depleted bovine alpha-lactalbumin (apo-BLA) have been studied by UV absorbance spectroscopy and transmission electron microscopy. The experimental results demonstrate that two unsaturated fatty acids, oleic acid and linoleic acid, and one saturated fatty acid, stearic acid, induce the intermediate of apo-BLA at pH 4.0-4.5 to form amorphous aggregates in time- and concentration-dependent manners. These aggregates are dissolved under physiological conditions at 37 degrees C and further characterized by fluorescence spectroscopy, circular dichroism and time-of-flight mass spectrometry. Our data here indicate that the structural characteristics of these aggregates are similar to those of HAMLET/BAMLET (human/bovine alpha-lactalbumin made lethal to tumor cells), a complex of the partially unfolded alpha-lactalbumin with oleic acid. Cell viability experiments indicate the aggregates of apo-BLA induced by oleic acid and linoleic acid show significant dose-dependent cytotoxicity to human lung tumor cells of A549 but those induced by stearic acid have no toxicity to tumor cells. Furthermore, the cytotoxic aggregates of apo-BLA induced by both unsaturated fatty acids induce apoptosis of human lung cancer cell line A549, suggesting that such cytotoxic aggregates of apo-BLA could be potential antitumor drugs. The present study provides insight into the mechanism of fatty acid-dependent oligomerization and cytotoxicity of alpha-lactalbumin, and will be helpful in the understanding of the molecular mechanism of HAMLET/BAMLET formation.

摘要

通过紫外吸收光谱和透射电子显微镜研究了三种脂肪酸对钙离子耗尽的牛α-乳白蛋白(脱辅基BLA)细胞毒性聚集体形成的影响。实验结果表明,两种不饱和脂肪酸油酸和亚油酸以及一种饱和脂肪酸硬脂酸,在pH 4.0 - 4.5条件下诱导脱辅基BLA中间体以时间和浓度依赖性方式形成无定形聚集体。这些聚集体在37℃生理条件下溶解,并通过荧光光谱、圆二色性和飞行时间质谱进一步表征。我们的数据表明,这些聚集体的结构特征与HAMLET/BAMLET(对肿瘤细胞具有致死性的人/牛α-乳白蛋白)相似,后者是部分展开的α-乳白蛋白与油酸的复合物。细胞活力实验表明,油酸和亚油酸诱导的脱辅基BLA聚集体对A549人肺肿瘤细胞具有显著的剂量依赖性细胞毒性,而硬脂酸诱导的聚集体对肿瘤细胞无毒性。此外,两种不饱和脂肪酸诱导的脱辅基BLA细胞毒性聚集体均可诱导人肺癌细胞系A549凋亡,表明这种脱辅基BLA细胞毒性聚集体可能是潜在的抗肿瘤药物。本研究为α-乳白蛋白脂肪酸依赖性寡聚化和细胞毒性机制提供了见解,并将有助于理解HAMLET/BAMLET形成的分子机制。

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