Tris(2-chloroethyl) phosphate (TCEP) exposure inhibits the epithelial-mesenchymal transition (EMT), mesoderm differentiation, and cardiovascular development in early chicken embryos

被引:2
|
作者
Kanda, Kazuki [1 ,2 ]
Iwata, Hisato [1 ]
机构
[1] Ehime Univ, Ctr Marine Environm Studies CMES, 2-5 Bunkyo Cho, Matsuyama, Ehime 7908577, Japan
[2] Natl Agr & Food Res Org, Natl Inst Anim Hlth, 3-1-5 Kannondai, Tsukuba, Ibaraki 3050856, Japan
基金
日本学术振兴会;
关键词
Ex ovo; OPFRs; OPEs; RNA-seq; Developmental toxicity; Adverse outcome pathway (AOP); ORGANOPHOSPHORUS FLAME RETARDANTS; CELL FATE SPECIFICATION; TRANSCRIPTION FACTORS; MOLECULAR-MECHANISMS; SIGNAL-TRANSDUCTION; EXPRESSION PATTERN; GENE; GROWTH; ENDOCRINE; ZEBRAFISH;
D O I
10.1016/j.scitotenv.2024.171242
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Tris(2-chloroethyl) phosphate (TCEP) is an organophosphorus flame retardant used worldwide and has been detected in the tissues and eggs of wild birds. Our previous study reported that exposure to TCEP induced developmental delay and cardiovascular dysfunction with attenuated heart rate and vasculogenesis in early chicken embryos. This study aimed to investigate the molecular mechanisms underlying the cardiovascular effects of TCEP on chicken embryos using cardiac transcriptome analysis and to examine whether TCEP exposure affects epithelial-mesenchymal transition (EMT) and mesoderm differentiation during gastrulation. Transcriptome analysis revealed that TCEP exposure decreased the expression of cardiac conduction -related genes and transcription factors on day 5 of incubation. In extraembryonic blood vessels, the expression levels of genes related to fibroblast growth factor (FGF) and vascular endothelial growth factor (VEGF) were significantly reduced by TCEP exposure and vasculogenesis was suppressed. TCEP exposure also attenuated Snail family transcriptional repressor 2 (SNAI2) and T -box transcription factor T (TBXT) signaling in the chicken primitive streak, indicating that TCEP inhibits EMT and mesoderm differentiation during gastrulation at the early developmental stage. These effects on EMT and mesoderm differentiation may be related to subsequent phenotypic defects, including suppression of heart development and blood vessel formation.
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页数:15
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