Transcriptomic response and perturbation of toxicity pathways in zebrafish larvae after exposure to graphene quantum dots (GQDs)

被引:44
|
作者
Deng, Shun [1 ,2 ]
Jia, Pan-Pan [2 ,3 ]
Zhang, Jing-Hui [2 ]
Junaid, Muhammad [2 ,3 ]
Niu, Aping [2 ]
Ma, Yan-Bo [2 ]
Fu, Ailing [1 ]
Pei, De-Sheng [1 ,2 ]
机构
[1] Southwest Univ, Coll Pharmaceut Sci, Chongqing 400715, Peoples R China
[2] Chinese Acad Sci, Chongqing Inst Green & Intelligent Technol, Chongqing 400714, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
GQDs; Signaling pathways; Transcriptome analysis; Zebrafish; WALLED CARBON NANOTUBES; TOLL-LIKE RECEPTORS; NF-KAPPA-B; IN-VITRO; MOLECULAR-MECHANISMS; OXIDE; WATER; EXPRESSION; RISKS; IDENTIFICATION;
D O I
10.1016/j.jhazmat.2018.05.063
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Graphene quantum dots (GQDs) are widely used for biomedical applications. Previously, the low-level toxicity of GQDs in vivo and in vitro has been elucidated, but the underlying molecular mechanisms remained largely unknown. Here, we employed the Illumina high-throughput RNA-sequencing to explore the whole-transcriptome profiling of zebrafish larvae after exposure to GQDs. Comparative transcriptome analysis identified 2116 differentially expressed genes between GQDs exposed groups and control. Functional classification demonstrated that a large proportion of genes involved in acute inflammatory responses and detoxifying process were significantly up-regulated by GQDs. The inferred gene regulatory network suggested that activator protein 1 (AP-1) was the early-response transcription factor in the linkage of a cascade of downstream (pro-) inflammatory signals with the apoptosis signals. Moreover, hierarchical signaling threshold determined the high sensitivity of complement system in zebrafish when exposed to the sublethal dose of GQDs. Further, 35 candidate genes from various signaling pathways were further validated by qPCR after exposure to 25, 50, and 100 mu g/mL of GQDs. Taken together, our study provided a valuable insight into the molecular mechanisms of potential bleeding risks and detoxifying processes in response to GQDs exposure, thereby establishing a mechanistic basis for the biosafety evaluation of GQDs.
引用
收藏
页码:146 / 158
页数:13
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