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桉油精和β-环柠檬醛诱导莱茵衣藻程序性细胞死亡的毒性机制。

Toxic mechanism of eucalyptol and β-cyclocitral on Chlamydomonas reinhardtii by inducing programmed cell death.

机构信息

State Key Laboratory of Subtropical Silviculture, Zhejiang A&F University, Hangzhou 311300, China; School of Forestry and Biotechnology, Zhejiang A&F University, Hangzhou 311300, China.

State Key Laboratory of Subtropical Silviculture, Zhejiang A&F University, Hangzhou 311300, China; School of Forestry and Biotechnology, Zhejiang A&F University, Hangzhou 311300, China.

出版信息

J Hazard Mater. 2020 May 5;389:121910. doi: 10.1016/j.jhazmat.2019.121910. Epub 2019 Dec 16.

DOI:10.1016/j.jhazmat.2019.121910
PMID:31879110
Abstract

Eucalyptol and β-cyclocitral are 2 main compounds in cyanobacterial volatile organic compounds and can poison other algae. To uncover the toxic mechanism of the 2 compounds, the cell growth, photosynthetic abilities, HO production, caspase-like activities, nuclear variation and DNA laddering were investigated in Chlamydomonas reinhardtii treated with eucalyptol and β-cyclocitral. Eucalyptol at ≥ 0.1 mM and β-cyclocitral at ≥ 0.05 mM showed toxic effects on C. reinhardtii cells, and 1.2 mM eucalyptol and 0.4 mM β-cyclocitral killed the whole of the cells during 24 h. During the death process, the photosynthetic pigment gradually degraded, and Fv/Fm gradually declined, indicating that the death is not a necrosis due to the gradual disappearance of the physiological process. In the treatments with 1.2 mM eucalyptol and 0.4 mM β-cyclocitral, HO content burst at 10 min and 30 min, respectively. Caspase-9-like and caspase-3-like were activated, and cell nucleuses concentrated firstly and then broke with prolonging the treatment time. Meanwhile, DNA showed laddering after 1 h, and was gradually cleaved by Ca-dependent endonucleases to mainly about 100-250 bp fragments. These hallmarks indicated that eucalyptol and β-cyclocitral may poison other algal cells by inducing programmed cell death triggered by the increased HO.

摘要

桉油精和β-环柠檬醛是蓝藻挥发性有机化合物中的 2 种主要化合物,可毒害其他藻类。为揭示这 2 种化合物的毒性机制,研究了桉油精和β-环柠檬醛处理莱茵衣藻后细胞生长、光合能力、HO 生成、半胱天冬酶样活性、核变异和 DNA 梯状带的变化。桉油精≥0.1mM 和β-环柠檬醛≥0.05mM 对莱茵衣藻细胞表现出毒性作用,1.2mM 桉油精和 0.4mM β-环柠檬醛在 24h 内杀死了全部细胞。在死亡过程中,光合色素逐渐降解,Fv/Fm 逐渐下降,表明死亡不是由于生理过程逐渐消失引起的坏死。在 1.2mM 桉油精和 0.4mM β-环柠檬醛处理中,HO 含量分别在 10min 和 30min 时爆发。半胱天冬酶-9 样和半胱天冬酶-3 样被激活,随着处理时间的延长,细胞核先浓缩,然后破裂。同时,1h 后 DNA 出现梯状带,随后被 Ca 依赖性核酸内切酶逐渐切割,主要产生 100-250bp 的片段。这些特征表明,桉油精和β-环柠檬醛可能通过诱导 HO 增加引发的程序性细胞死亡来毒害其他藻类细胞。

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