Tris(1,3-dichloro-2-propyl) phosphate reduces longevity through a specific microRNA-mediated DAF-16/FoxO in an unconventional insulin/insulin-like growth factor‑1 signaling pathway

Tris(1,3-dichloro-2-propyl) phosphate (TDCPP) has received concerns due to its frequent detection in environmental media and biological samples. Our previous study has indicated TDCPP reduced the lifespan of Caenorhabditis elegans (C. elegans) by triggering an unconventional insulin/insulin-like gro...

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Veröffentlicht in:Journal of hazardous materials 2022-03, Vol.425, p.128043-128043, Article 128043
Hauptverfasser: Wang, Chen, Li, Yeyong, Zeng, Lingjun, Shi, Chongli, Peng, Yi, Li, Hui, Chen, Haibo, Yu, Jun, Zhang, Jin, Cheng, Biao, Pan, Ruolin, Wang, Xiaoli, Xiang, Minghui, Huang, Yuan, Liu, Yongdi
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Sprache:eng
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Zusammenfassung:Tris(1,3-dichloro-2-propyl) phosphate (TDCPP) has received concerns due to its frequent detection in environmental media and biological samples. Our previous study has indicated TDCPP reduced the lifespan of Caenorhabditis elegans (C. elegans) by triggering an unconventional insulin/insulin-like growth factor signaling (IIS) pathway. This study continued to investigate the possible deleterious effects of TDCPP relating to longevity regulation signal pathways and biological processes. Specifically, this study uniquely performed small RNA transcriptome sequencing (RNA-seq), focusing on the underlying mechanisms of TDCPP-reduced the longevity of C. elegans in-depth in microRNAs (miRNAs). Based on Small RNA-seq results and transcript levels of mRNA involved in the unconventional IIS pathway, a small interaction network of miRNAs-mRNAs following TDCPP exposure in C. elegans was preliminarily established. Among them, up-regulated miR-48 and miR-84 (let-7 family members) silence the mRNA of daf-16 (the crucial member of the FoxO family and pivotal regulator in longevity) via post-transcription and translation dampening abilities, further inhibit its downstream target metallothionein-1 (mtl-1), and ultimately contributed to the reduction of nematode longevity and locomotion behaviors. Meanwhile, the high binding affinities of TDCPP with miRNAs cel-miR-48–5p and cel-miR-84–5p strongly support their participation in the regulation of nematode mobility and longevity. These findings provide a comprehensive analysis of TDCPP-reduced longevity from the perspective of miRNAs. [Display omitted] •Small RNA-seq following TDCPP exposure were uniquely performed.•The prediction of miRNA was highly consistent with the unconventional IIS pathway.•An interactive network of miRNAs-mRNAs regulating longevity was established.•TDCPP specific bindings miR-48 and miR-84 with high docking score.•Up-regulated miR-48 and miR-84 silence the daf-16 and ultimately reduce longevity.
ISSN:0304-3894
1873-3336
DOI:10.1016/j.jhazmat.2021.128043