Regulation of Hox and ParaHox genes by perfluorochemicals in mouse liver. (August 2020)

• Record Type: Journal Article
• Authors: Zhang, Yue; Le, Yuan; Bu, Pengli; Cheng, Xingguo
• Is Part Of: Toxicology. Volume 441(2020)
• Publication Date: 2020-08
• Subjects: CAR constitutive androstane receptor -- Cdx caudal-related homeobox -- DR direct repeat -- EMT epithelial-mesenchymal transition -- Gsx GS homeobox -- MMP matrix metallopeptidase -- Nrf2 nuclear factor erythroid 2-related factor 2 -- Pdx pancreatic and duodenal homeobox -- PFCs perfluorinated chemicals -- PFDA perfluorodecanoic acid -- PFNA perfluorononanoic acid -- PFOA perfluorooctanoic acid -- PPARα peroxisome proliferator-activated receptor alpha -- PPRE peroxisome proliferator-activated receptor response element -- TCPOBOP 1, 4-bis[2-(3, 5-dichloropyridyloxy)]benzene; Hox gene -- Perfluorinated chemicals -- PPARα; Toxicology -- Periodicals; Chemicals -- Physiological effect -- Periodicals; 615.9005
• DOI: 10.1016/j.tox.2020.152521
• Languages: English
• ISSNs: 0300-483X

Abstract

Abstract: Homeobox (Hox) genes encode homeodomain proteins, which play important roles in the development and morphological diversification of organisms including plants and animals. Perfluorinated chemicals (PFCs), which are well recognized industrial pollutants and universally detected in human and wildlife, interfere with animal development. In addition, PFCs produce a number of hepatic adverse effects, such as hepatomegaly and dyslipidemia. Homeodomain proteins profoundly contribute to liver regeneration. Hox genes serve as either oncogenes or tumor suppressor genes during target organ carcinogenesis. However, to date, no study investigated whether PFCs regulate expression of Hox genes. This study was designed to determine the regulation of Hox (including Hox-a to -d subfamily members) and paraHox [including GS homeobox (Gsx), pancreatic and duodenal homeobox (Pdx), and caudal-related homeobox (Cdx) family members] genes by PFCs including perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), and perfluorodecanoic acid (PFDA) in mouse liver. 46.4 mg/kg PFNA induced mRNA expression of Hoxa5, b7, c5, d10 and Pdx1 in wild-type and CAR-null mouse livers, but not in PPARα-null mouse livers, indicating a PPARα-dependent manner. PFOA, PFNA, and PFDA all induced mRNA expression of Hoxa5, b7, c5, d10, Pdx1 and Zeb2 in wild-type but not PPARα-null mouse livers. In addition, in Nrf2-null mouse livers, PFNA continued to increase mRNA expression of Hoxa5 and Pdx1, but not Hoxb7, c5 or d10. Furthermore, Wy14643, a classical PPARα agonist, induced mRNA expression of Hoxb7 and c5 in wild-type but not PPARα-null mouse livers. However, Wy14643 did not induce mRNA expression of Hoxa5, d10 or Pdx1 in either wild-type or PPARα-null mouse livers. TCPOBOP, a classical mouse CAR agonist, increased mRNA expression of Hoxb7, c5 and d10 but not Hoxa5 or Pdx1 in mouse livers. Moreover, PFNA decreased cytoplasmic and nuclear Hoxb7 protein levels in mouse livers. However, PFNA increased cytoplasmic Hoxc5 protein level but decreased nuclear Hoxc5 protein level in mouse livers. In conclusion, PFCs induced mRNA expression of several Hox genes such as Hoxb7, c5 and d10, mostly through the activation of PPARα and/or Nrf2 signaling.