Recent in vitro transcriptomic analyses for short-chain per- and polyfluoroalkyl substances HFPO-DA (ammonium, 2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)-propanoate) added to the weight of evidence supporting the peroxisome proliferator-activated receptor alpha (PPARα) activator-induced hepatocarcinogenesis mode of action (MOA) for HFPO-DA-mediated liver effects in rodents. Importantly, PPARα-mediated key events (KEs) including hepatocellular hypertrophy and proliferation that have been shown to occur prior to tumor development in this MOA are rodent-specific and likely not human-relevant. To further inform the MOA of HFPO-DA and evaluate other hypothesized MOAs, phenotypic and transcriptomic responses in wild-type (WT) and Ppara-null mice were investigated following short-term exposure to HFPO-DA or prototypical agonists of PPARα (GW7647), PPARγ (rosiglitazone), or cytotoxicity (acetaminophen). Phenotypic and transcriptomic assessment of mouse livers demonstrated a general lack of response to HFPO-DA or GW7647 exposure in Ppara-null but not WT mice. Conversely, rosiglitazone or acetaminophen elicited similar phenotypic and transcriptomic responses between genotypes demonstrating a lack of PPARα-dependence. In WT mice, HFPO-DA-mediated responses were similar to GW7647 but different from rosiglitazone or acetaminophen. Dose-dependent increases in liver weight, karyomegaly, and mitosis, as well as increased transcriptomic signaling related to PPARα activation and cell proliferation were observed in HFPO-DA and GW7647-exposed WT mice. The consistent phenotypic and transcriptomic signaling patterns between HFPO-DA and GW7647 in WT mice, and the lack of changes in Ppara-null mice, provide further support that HFPO-DA-mediated early KEs in mouse liver are PPARα-dependent, occur via the rodent-specific PPARα MOA, and therefore are not appropriate for use in human health risk assessment.
Comparison of phenotypic and transcriptomic profiles between HFPO-DA and prototypical PPARα, PPARγ, and cytotoxic agents in wild-type and Ppara-null mouse livers.
比较 HFPO-DA 与原型 PPARα、PPARα³ 和细胞毒性药物在野生型和 Ppara 基因敲除小鼠肝脏中的表型和转录组特征
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作者:Heintz Melissa M, Buerger Amanda N, Haws Laurie C, Cullen John M, East Alexander W, Thompson Chad M
| 期刊: | Toxicological Sciences | 影响因子: | 4.100 |
| 时间: | 2025 | 起止号: | 2025 Jul 1; 206(1):183-201 |
| doi: | 10.1093/toxsci/kfaf049 | 种属: | Mouse |
| 研究方向: | 细胞生物学 | ||
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