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全氟辛酸诱导鸡胚发育性心脏毒性:miR-490-5p 的作用。

Perfluorooctanoic acid-induced developmental cardiotoxicity in chicken embryo: Roles of miR-490-5p.

机构信息

Department of Toxicology, School of Public Health, Qingdao University, China.

Department of Special Medicine, School of Basic Medicine, Qingdao University, China.

出版信息

Environ Pollut. 2022 Nov 1;312:120022. doi: 10.1016/j.envpol.2022.120022. Epub 2022 Aug 23.

Abstract

Perfluorooctanoic acid (PFOA) could induce developmental toxicities, affecting various organs, including the heart. Although peroxisome-proliferation activated receptor alpha (PPARα) had been identified as a major target of PFOA, PPARα-independent effects are frequently reported. To further elucidate the mechanism of toxicity in PFOA-induced developmental cardiotoxicity, RNA-seq analysis was performed in hatchling chicken hearts developmentally exposed to vehicle or 2 mg/kg (egg weight) PFOA. RT-PCR and western blotting were then performed to confirm the identified potential targets. Furthermore, lentivirus was designed to overexpress and silence identified target miRNA in developing chicken embryo, and the resulting phenotypes were investigated. 21 miRNAs and 1142 mRNAs were identified to be affected by developmental exposure to PFOA in chicken embryo hearts. Among the identified differentially expressed miRNAs, miR-490-5p was confirmed to be significantly affected by PFOA exposure, along with its downstream targets, Synaptosome associated protein 91 (SNAP91) and LY6/PLAUR domain containing 6 (LYPD6), as indicated by RT-PCR and western blotting results. Lentivirus overexpressing miR-490-5p mimicked the phenotype induced by PFOA exposure, while lentivirus silencing miR-490-5p alleviated PFOA-induced changes. Similar patterns were also observed in the expression of downstream target genes, SNAP91 and LYPD6. In summary, miR-490-5p and its downstream genes, SNAP91 and LYPD6 are associated with PFOA-induced developmental cardiotoxicity in chicken embryo, which might help to further elucidate the mechanism of PFOA-induced developmental cardiotoxicity.

摘要

全氟辛酸(PFOA)可诱导发育毒性,影响包括心脏在内的各种器官。虽然过氧化物酶体增殖物激活受体α(PPARα)已被确定为 PFOA 的主要靶标,但经常报道其存在非依赖性效应。为了进一步阐明 PFOA 诱导的发育性心脏毒性的毒性机制,对发育过程中暴露于载体或 2mg/kg(卵重)PFOA 的雏鸡心脏进行了 RNA-seq 分析。然后进行 RT-PCR 和 Western blot 以验证鉴定的潜在靶标。此外,设计了慢病毒在发育中的鸡胚中过表达和沉默鉴定的靶标 miRNA,并研究了由此产生的表型。在鸡胚心脏中,有 21 个 miRNA 和 1142 个 mRNA 因胚胎发育暴露于 PFOA 而受到影响。在所鉴定的差异表达 miRNA 中,miR-490-5p 被证实受 PFOA 暴露的显著影响,其下游靶标突触相关蛋白 91(SNAP91)和 LY6/PLAUR 结构域包含 6(LYPD6)也通过 RT-PCR 和 Western blot 结果得到证实。过表达 miR-490-5p 的慢病毒模拟了 PFOA 暴露引起的表型,而沉默 miR-490-5p 的慢病毒减轻了 PFOA 诱导的变化。下游靶基因 SNAP91 和 LYPD6 的表达也观察到类似的模式。总之,miR-490-5p 及其下游基因 SNAP91 和 LYPD6 与鸡胚中 PFOA 诱导的发育性心脏毒性有关,这可能有助于进一步阐明 PFOA 诱导的发育性心脏毒性的机制。

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