Transcriptional and Proteomic Analysis Revealed a Synergistic Effect of Aflatoxin M1 and Ochratoxin A Mycotoxins on the Intestinal Epithelial Integrity of Differentiated Human Caco-2 Cells.
Yanan GaoSongli LiXiaoyu BaoChaochao LuoHuaigu YangJiaqi WangShengguo ZhaoNan ZhengPublished in: Journal of proteome research (2018)
Aflatoxin M1 (AFM1) is a common mycotoxin in dairy milk, and it is typically concurrently present with other mycotoxins that may represent a threat to food safety. However, knowledge of how AFM1, alone or in combination with other mycotoxins, may affect human intestinal epithelial integrity remain to be established. We employed transcriptome and proteome analysis integrated with biological validation to reveal the molecular basis underlining the effect of exposure to AFM1, ochratoxin A (OTA), or both on the intestinal epithelial integrity of differentiated Caco-2 cells. Exposure to 4 μg/mL of OTA was found to disrupt human gut epithelial integrity, whereas 4 μg/mL of AFM1 did not. The integrated transcriptome and proteome analysis of AFM1 and OTA, alone or in combination, indicate the synergistic effect of the two mycotoxins in disrupting intestinal integrity. This effect was mechanistically linked to a broad range of pathways related to intestinal integrity enriched by down-regulated genes and proteins, associated with focal adhesion, adheren junction, and gap junction pathways. Furthermore, the cross-omics analysis of mixed AFM1 and OTA compared to OTA alone suggest that kinase family members, including myosin light-chain kinase, mitogen-activated protein kinases, and protein kinase C, are the potential key regulators in modulating intestinal epithelial integrity. These findings provide novel insight into the synergistic detrimental role of multiple mycotoxins in disrupting intestinal integrity and, therefore, identify potential targets to improve milk safety related to human health.
Keyphrases
- human health
- endothelial cells
- high speed
- atomic force microscopy
- protein kinase
- single cell
- gene expression
- risk assessment
- genome wide
- induced apoptosis
- transcription factor
- healthcare
- rna seq
- induced pluripotent stem cells
- dna methylation
- signaling pathway
- cell cycle arrest
- escherichia coli
- pluripotent stem cells
- climate change
- cystic fibrosis
- drug delivery
- oxidative stress
- staphylococcus aureus
- cancer therapy
- drug induced
- genome wide identification