The NLRP3-Mediated Neuroinflammatory Responses to CdTe Quantum Dots and the Protection of ZnS Shell
The NLRP3-Mediated Neuroinflammatory Responses to CdTe Quantum Dots and the Protection of ZnS Shell
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NLRP3 介导的 CdTe 量子点神经炎症反应和 ZnS 壳的保护
DOI:
10.2147/ijn.s246578
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发表时间:
2020-05
影响因子:
8
通讯作者:
Meng Tang
中科院分区:
文献类型:
--
作者:
Tianshu Wu;Xue Liang;Keyu He;Xi Liu;Yimeng Li;Yutong Wang;Lu Kong;Meng Tang
Introduction Since CdTe quantum dots (QDs) are still widely considered as advanced fluorescent probes because of their far superior optical performance and fluorescence efficiency over non-cadmium QDs, it is important to find ways to control their toxicity. Methods In this study, the adverse effects of two cadmium-containing QDs, ie, CdTe QDs and CdTe@ZnS QDs, on the nervous system of nematode C. elegans, the hippocampus of mice, and cultured microglia were measured in order to evaluate the neuroinflammation caused by cadmium-containing QDs and the potential mechanisms. Results Firstly, we observed that cadmium-containing QD exposure-induced immune responses and neurobehavioral deficit in nematode C. elegans. In the mice treated with QDs, neuroinflammatory responses to QDs in the hippocampus, including microglial activation and IL-1ß release, occurred as well. When investigating the mechanisms of cadmium-containing QDs causing IL-1ß-mediated inflammation, the findings suggested that cadmium-containing QDs activated the NLRP3 inflammasome by causing excessive ROS generation, and resulted in IL-1ß release. Discussion Even though the milder immune responses and neurotoxicity of CdTe@ZnS QDs compared with CdTe QDs indicated the protective role of ZnS coating, the inhibitions of NLRP3 expression and ROS production completely reduced the IL-1ß-mediated inflammation. This provided valuable information that inhibiting target molecules is an effective and efficient way to alleviate the toxicity of cadmium-containing QDs, so it is important to evaluate QDs through a mechanism-based risk assessment.
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影响因子:
9.9
作者:
Bujnakova, Zdenka;Balaz, Matej;Psotka, Miroslav
通讯作者:
Psotka, Miroslav
影响因子:
8.9
作者:
Takafumi Kimura;T. Takanami;T. Sakashita;S. Wada;Y. Kobayashi;A. Higashitani
通讯作者:
Takafumi Kimura;T. Takanami;T. Sakashita;S. Wada;Y. Kobayashi;A. Higashitani
影响因子:
10.4
作者:
Patchin ES;Anderson DS;Silva RM;Uyeminami DL;Scott GM;Guo T;Van Winkle LS;Pinkerton KE
通讯作者:
Pinkerton KE
影响因子:
3.8
作者:
Park HH;Jung Y;Lee SV
通讯作者:
Lee SV
DOI:
10.1002/bio.3193
发表时间:
2017-05
期刊:
Luminescence : the journal of biological and chemical luminescence
影响因子:
--
作者:
D. Saikia;S. Chakravarty;N. S. Sarma;S. Bhattacharjee;P. Datta;N. C. Adhikary
通讯作者:
D. Saikia;S. Chakravarty;N. S. Sarma;S. Bhattacharjee;P. Datta;N. C. Adhikary