Function of RSKS-1-AAK-2-DAF-16 signaling cascade in enhancing toxicity of multi-walled carbon nanotubes can be suppressed by mir-259 activation in Caenorhabditis elegans.

Autor: Zhuang Z; School of Pharmaceutical Engineering and Life Sciences, Changzhou University, Changzhou 213164, China.; Changzhou No. 7 People's Hospital, Changzhou 213011, China., Li M; School of Pharmaceutical Engineering and Life Sciences, Changzhou University, Changzhou 213164, China.; Key Laboratory of Environmental Medicine Engineering in Ministry of Education, Medical School, Southeast University, Nanjing 210009, China., Liu H; School of Pharmaceutical Engineering and Life Sciences, Changzhou University, Changzhou 213164, China., Luo L; Changzhou No. 7 People's Hospital, Changzhou 213011, China., Gu W; Changzhou No. 7 People's Hospital, Changzhou 213011, China., Wu Q; Key Laboratory of Environmental Medicine Engineering in Ministry of Education, Medical School, Southeast University, Nanjing 210009, China., Wang D; Key Laboratory of Environmental Medicine Engineering in Ministry of Education, Medical School, Southeast University, Nanjing 210009, China.
Jazyk: angličtina
Zdroj: Scientific reports [Sci Rep] 2016 Aug 30; Vol. 6, pp. 32409. Date of Electronic Publication: 2016 Aug 30.
DOI: 10.1038/srep32409
Abstrakt: Caenorhabditis elegans is an important non-mammalian alternative assay model for toxicological study. Previous study has indicated that exposure to multi-walled carbon nanotubes (MWCNTs) dysregulated the transcriptional expression of mir-259. In this study, we examined the molecular basis for mir-259 in regulating MWCNTs toxicity in nematodes. Mutation of mir-259 induced a susceptible property to MWCNTs toxicity, and MWCNTs exposure induced a significant increase in mir-259::GFP in pharyngeal/intestinal valve and reproductive tract, implying that mir-259 might mediate a protection mechanisms for nematodes against MWCNTs toxicity. RSKS-1, a putative ribosomal protein S6 kinase, acted as the target for mir-259 in regulating MWCNTs toxicity, and mutation of rsks-1 suppressed the susceptible property of mir-259 mutant to MWCNTs toxicity. Moreover, mir-259 functioned in pharynx-intestinal valve and RSKS-1 functioned in pharynx to regulate MWCNTs toxicity. Furthermore, RSKS-1 regulated MWCNTs toxicity by suppressing the function of AAK-2-DAF-16 signaling cascade. Our results will strengthen our understanding the microRNAs mediated protection mechanisms for animals against the toxicity from certain nanomaterials.
Databáze: MEDLINE