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氨基葡萄糖通过刺激人神经胶质瘤细胞内质网应激诱导自噬性细胞死亡。

Glucosamine induces autophagic cell death through the stimulation of ER stress in human glioma cancer cells.

机构信息

Chronic Disease Research Center, Keimyung University, Daegu, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2010 Aug 13;399(1):111-6. doi: 10.1016/j.bbrc.2010.07.050. Epub 2010 Jul 17.

Abstract

Autophagy can promote cell survival or death, but the molecular basis of its dual role in cancer is not well understood. Here, we report that glucosamine induces autophagic cell death through the stimulation of endoplasmic reticulum (ER) stress in U87MG human glioma cancer cells. Treatment with glucosamine reduced cell viability and increased the expression of LC3 II and GFP-LC3 fluorescence puncta, which are indicative of autophagic cell death. The glucosamine-mediated suppression of cell viability was reversed by treatment with an autophagy inhibitor, 3-MA, and interfering RNA against Atg5. Glucosamine-induced ER stress was manifested by the induction of BiP, IRE1alpha, and phospho-eIF2alpha expression. Chemical chaperon 4-PBA reduced ER stress and thereby inhibited glucosamine-induced autophagic cell death. Taken together, our data suggest that glucosamine induces autophagic cell death by inducing ER stress in U87MG glioma cancer cells and provide new insight into the potential anticancer properties of glucosamine.

摘要

自噬可以促进细胞存活或死亡,但自噬在癌症中双重作用的分子基础尚不清楚。在这里,我们报道了氨基葡萄糖通过刺激内质网(ER)应激诱导 U87MG 人神经胶质瘤癌细胞发生自噬性细胞死亡。氨基葡萄糖处理降低了细胞活力,并增加了 LC3 II 和 GFP-LC3 荧光斑点的表达,这表明发生了自噬性细胞死亡。自噬抑制剂 3-MA 和针对 Atg5 的干扰 RNA 逆转了氨基葡萄糖介导的细胞活力抑制。氨基葡萄糖诱导的 ER 应激表现为 BiP、IRE1alpha 和磷酸化 eIF2alpha 的表达诱导。化学伴侣 4-PBA 降低了 ER 应激,从而抑制了氨基葡萄糖诱导的自噬性细胞死亡。总之,我们的数据表明,氨基葡萄糖通过在 U87MG 神经胶质瘤癌细胞中诱导 ER 应激诱导自噬性细胞死亡,并为氨基葡萄糖的潜在抗癌特性提供了新的见解。

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