4.7 Article

Whole-Transcriptome Analysis of Non-Coding RNA Alteration in Porcine Alveolar Macrophage Exposed to Aflatoxin B1

Journal

TOXINS
Volume 14, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/toxins14060373

Keywords

aflatoxin B1; porcine; porcine alveolar macrophages; apoptosis; cell cycle

Funding

  1. High level talents research fund project of Qingdao Agricultural University in China [1120043]
  2. Science & Technology Fund Planning Projects of Qingdao City [21-1-4-ny-7-nsh]
  3. Natural Science Foundation of Shandong Province of China [ZR2021MC191]
  4. Taishan Scholar Construction Foundation of Shandong province of China [ts20190946]
  5. Cultivating Fund of Capital Medical University [PYZ2017002]
  6. Gene expression analysis of hormone receptor-negative breast cancer with low HER-2 expression and its potential influence on neoadjuvant chemotherapy [212102310658]

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The exposure to AFB1 impairs the proliferation of 3D4/2 cells and induces apoptosis through the non-coding RNA-mediated pathway.
Aflatoxin B1 (AFB1) is a type of mycotoxin produced by the fungi Aspergillus flavus and Aspergillus parasiticus and is commonly found in cereals, oils and foodstuffs. In order to understand the toxic effects of AFB1 exposure on Porcine alveolar macrophages (3D4/2 cell), the 3D4/2 cells were exposed to 40 mu g/mL AFB1 for 24 h in vitro, and several methods were used for analysis. Edu and TUNEL analysis showed that the proliferation of 3D4/2 cells was significantly inhibited and the apoptosis of 3D4/2 cells was significantly induced after AFB1 exposure compared with that of the control group. Whole-transcriptome analysis was performed to reveal the non-coding RNA alteration in 3D4/2 cells after AFB1 exposure. It was found that the expression of cell-cycle-related and apoptosis-related genes was altered after AFB1 exposure, and lncRNAs and miRNAs were also significantly different among the experimental groups. In particular, AFB1 exposure affected the expression of lncRNAs associated with cellular senescence signaling pathways, such as MSTRG.24315 and MSTRG.80767, as well as related genes, Cxcl8 and Gadd45g. In addition, AFB1 exposure affected the expression of miRNAs associated with immune-related genes, such as miR-181a, miR-331-3p and miR-342, as well as immune-related genes Nfkb1 and Rras2. Moreover, the regulation networks between mRNA-miRNAs and mRNA-lncRNAs were confirmed by the results of RT-qPCR and immunofluorescence. In conclusion, our results here demonstrate that AFB1 exposure impaired proliferation of 3D4/2 cells via the non-coding RNA-mediated pathway.

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