Detailed characterization of alterations in the lipid profiles during autophagic cell death of leukemia cells

被引:10
作者
Lee, Jae Won [1 ,2 ]
Shinohara, Haruka [3 ]
Jung, Jae Hun [1 ]
Mok, Hyuck Jun [1 ]
Akao, Yukihiro [3 ]
Kim, Kwang Pyo [1 ,4 ]
机构
[1] Kyung Hee Univ, Coll Appl Sci, Dept Appl Chem, Yongin 446701, South Korea
[2] RDA, Natl Inst Hort & Herbal Sci, Dept Herbal Crop Res, Eumseong 369873, South Korea
[3] Gifu Univ, United Grad Sch Drug Discovery & Med Informat Sci, 1-1 Yanagido, Gifu 5011193, Japan
[4] Kyung Hee Univ, Inst Nat Sci, Coll Appl Sci, Yongin 446701, South Korea
来源
RSC ADVANCES | 2016年 / 6卷 / 35期
基金
新加坡国家研究基金会;
关键词
ACID; METABOLISM; INDUCTION; SURVIVAL; DROPLETS; STORAGE; STORES;
D O I
10.1039/c6ra01965j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, a lipidomics approach based on UPLC-QqQ/MS was applied to profile various lipids in human leukemia cells undergoing autophagic cell death (ACD). Our previous study indicated that AIC-47, a 3-decenoic acid derivative, induced ACD in cancer cells that was associated with lipophagy. To understand the altered metabolism of lipids during ACD, 23 lipid classes were profiled in AIC-47 - treated cancer cells. Using the optimal UPLC conditions, individual lipid species were well separated in 30 min. By multiple reaction monitoring the 397 individual lipid species were successfully identified and quantified. 14 classes of lipid-TG, DG, PS, PG, PI, PA, LPC, LPE, LPS, LPG, LPI, Cer, Sa, and Cer1P-were upregulated and 3 classes-ChE, PC, and LPA-were downregulated in the ACD-induced cells compared to the control (P <= 0.05 by t-test). Other classes, such as PE, SM, dCer, So, So1P, and Sa1P, showed no changes. These results indicate that lipid metabolism of ACD is related to the mechanism of autophagy.
引用
收藏
页码:29512 / 29518
页数:7
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