* Department of Clinical Laboratory, Shanghai Putuo District People's Hospital, Shanghai, China.
† Department of Oncology, Clinical Research Institute, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, China.
Am J Chin Med. 2018;46(3):673-687. doi: 10.1142/S0192415X18500350. Epub 2018 Apr 4.
Curcumin is a hydrophobic polyphenol derived from turmeric: the rhizome of the herb Curcumalonga. Autophagy is an evolutionarily conserved process, in which cellular proteins and organelles are engulfed in autophagosome and then fuses with lysosome for degradation. Our previous study showed that Curcumin activates lysosome and induce autophagy through inhibition of AKT (protein kinase K, PKB)-mammalian target of rapamycin (mTOR) pathway. But whether Curucmin affects the fusion of autophagosome-lysosome is still not clear. Here, we used Curcumin-probe conjugation with an alkyne moiety to label mouse embryonic fibroblasts (MEFs) and found that Curcumin targets autophagy-related proteins, enhances autophagic flux and activates lysosome in cells. Moreover, Curcumin treatment promotes the fusion of autophasosome-lysosome in MEFs. Second, the enhanced fusion of autophagosome-lysosome is attributed to mTOR suppression. Third, blockage of the autophagosome-lysosome fusion leads to cell growth inhibition by Curcumin. Taken together, data from our study indicates the importance of the fusion of autophagosome-lysosome in Curcumin-induced autophagy, which may facilitate the development of Curcumin as a potential therapeutic agent for oxidative stress-related diseases.
姜黄的根茎。自噬是一种进化上保守的过程,其中细胞蛋白质和细胞器被自噬体吞噬,然后与溶酶体融合进行降解。我们之前的研究表明,姜黄素通过抑制 AKT(蛋白激酶 K,PKB)-雷帕霉素靶蛋白(mTOR)途径来激活溶酶体并诱导自噬。但是,姜黄素是否影响自噬体-溶酶体的融合仍然不清楚。在这里,我们使用带有炔基部分的姜黄素探针缀合来标记小鼠胚胎成纤维细胞(MEFs),发现姜黄素靶向自噬相关蛋白,增强自噬流并在细胞中激活溶酶体。此外,姜黄素处理可促进 MEFs 中自噬体-溶酶体的融合。其次,增强的自噬体-溶酶体融合归因于 mTOR 抑制。第三,自噬体-溶酶体融合的阻断导致姜黄素引起的细胞生长抑制。总之,我们的研究数据表明自噬体-溶酶体融合在姜黄素诱导的自噬中的重要性,这可能有助于将姜黄素开发为氧化应激相关疾病的潜在治疗剂。