The potential toxic effects of cerium on organism: cerium prolonged the developmental time and induced the expression of Hsp70 and apoptosis in Drosophila melanogaster

被引:11
作者
Wu, Bin [1 ,2 ]
Zhang, Di [1 ]
Wang, Dan [1 ]
Qi, Chunyan [1 ]
Li, Zongyun [1 ]
机构
[1] Jiangsu Normal Univ, Inst Cellular & Mol Biol, Sch Life Sci, Xuzhou 221116, Jiangsu, Peoples R China
[2] Peking Union Med Coll, Grad Sch, Beijing 100730, Peoples R China
基金
中国国家自然科学基金;
关键词
Apoptosis; Cerium; Developmental time; D; melanogaster; DNA damage; RARE-EARTH ELEMENTS; DNA-DAMAGE; TRANSGENIC DROSOPHILA; P53; STRESS; ACTIVATION; PATHWAYS; METALLOTHIONEIN; INDUCTION; CASPASE-3;
D O I
10.1007/s10646-012-0960-x
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Due to the widespread application of cerium, a rare earth element, the risk of exposure to cerium has increased. Therefore, understanding the physiological effects of cerium is of great importance. Our previous work showed that cerium caused significant lifespan shortening accompanied by oxidative damage in Drosophila melanogaster, however, little is known about the detailed mechanism of cerium-induced cytotoxicity. Thus, we examined the developmental time during metamorphosis, and assessed the toxic effects of cerium by evaluating heat shock protein 70 (Hsp70), DNA damage markers and apoptosis in D. melanogaster. We found that cerium extended the developmental time of D. melanogaster and up-regulated the expression of Hsp70 when the concentration of cerium was increased (especially concentrations over 26.3 mu g/g). Up-regulation of the cell cycle checkpoint p53 and cell signaling protein p38 were also observed when the concentration of cerium was over 104 mu g/g. In addition, the activities of caspase-3 and caspase-9, markers of apoptosis, were significantly higher when the larvae were exposed to ceric sulfate. These results suggest that high concentrations of cerium may result in DNA damage and ultimately apoptosis in D. melanogaster, and strongly indicate that cerium should be applied with caution and the potential toxic effects in humans should also be taken into consideration.
引用
收藏
页码:2068 / 2077
页数:10
相关论文
共 36 条
  • [31] HSP70 attenuates compression-induced apoptosis of nucleus pulposus cells by suppressing mitochondrial fission via upregulating the expression of SIRT3
    Hu, Binwu
    Wang, Peng
    Zhang, Shuo
    Liu, Weijian
    Lv, Xiao
    Shi, Deyao
    Zhao, Lei
    Liu, Hongjian
    Wang, Baichuan
    Chen, Songfeng
    Shao, Zengwu
    [J]. EXPERIMENTAL AND MOLECULAR MEDICINE, 2022, 54 (03) : 309 - 323
  • [32] Curcumin Increases HSP70 Expression in Primary Rat Cortical Neuronal Apoptosis Induced by gp120 V3 Loop Peptide
    Chenglai Xia
    Yantao Cai
    Shuhua Li
    Jie Yang
    Guohong Xiao
    [J]. Neurochemical Research, 2015, 40 : 1996 - 2005
  • [33] Hsp70 expression induced by Co-Enzyme Q10 protected chicken myocardial cells from damage and apoptosis under in vitro heat stress
    Xu, J.
    Tang, S.
    Song, E.
    Yin, B.
    Wu, D.
    Bao, E.
    [J]. POULTRY SCIENCE, 2017, 96 (05) : 1426 - 1437
  • [34] Effects of Taurine on ACE, ACE2 and HSP70 Expression of Hypothalamic-Pituitary-Adrenal Axis in Stress-Induced Hypertensive Rats
    Lv, Qiufeng
    Yang, Qunhui
    Cui, Yiqing
    Yang, Jiancheng
    Wu, Gaofeng
    Liu, Mei
    Ning, Zhili
    Cao, Shuang
    Dong, Gonglin
    Hu, Jianmin
    [J]. TAURINE 10, 2017, 975 : 871 - 886
  • [35] Concentration-dependent differential effects of N-acetyl-L-cysteine on the expression of HSP70 and metallothionein genes induced by cadmium in human amniotic cells
    Abe, T
    Yamamura, K
    Gotoh, S
    Kashimura, M
    Higashi, K
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1998, 1380 (01): : 123 - 132
  • [36] Suppression of HSP70 expression sensitizes NSCLC cell lines to TRAIL-induced apoptosis by upregulating DR4 and DR5 and downregulating c-FLIP-L expressions
    Zhuang, Hongqin
    Jiang, Weiwei
    Zhang, Xiangyu
    Qiu, Fan
    Gan, Ziyi
    Cheng, Wei
    Zhang, Jing
    Guan, Shengwen
    Tang, Bo
    Huang, Qilai
    Wu, Xinhua
    Huang, Xiaofeng
    Jiang, Wenhui
    Hu, Qingang
    Lu, Min
    Hua, Zi-Chun
    [J]. JOURNAL OF MOLECULAR MEDICINE-JMM, 2013, 91 (02): : 219 - 235