The Dysregulation of Inflammatory Pathways Triggered by Copper Exposure.
Huidan DengSong ZhuHuiru YangHengmin CuiHongrui GuoJunliang DengZhihua RenYi GengPing OuyangZhiwen XuYoutian DengYanqiu ZhuPublished in: Biological trace element research (2022)
Copper (Cu) is an essential micronutrient for both human and animals. However, excessive intake of copper will cause damage to organs and cells. Inflammation is a biological response that can be induced by various factors such as pathogens, damaged cells, and toxic compounds. Dysregulation of inflammatory responses are closely related to many chronic diseases. Recently, Cu toxicological and inflammatory effects have been investigated in various animal models and cells. In this review, we summarized the known effect of Cu on inflammatory responses and sum up the molecular mechanism of Cu-regulated inflammation. Excessive Cu exposure can modulate a huge number of cytokines in both directions, increase and/or decrease through a variety of molecular and cellular signaling pathways including nuclear factor kappa-B (NF-κB) pathway, mitogen-activated protein kinase (MAPKs) pathway, JAK-STAT (Janus Kinase- signal transducer and activator of transcription) pathway, and NOD-like receptor protein 3 (NLRP3) inflammasome. Underlying the molecular mechanism of Cu-regulated inflammation could help further understanding copper toxicology and copper-associated diseases.
Keyphrases
- nuclear factor
- oxidative stress
- induced apoptosis
- signaling pathway
- cell cycle arrest
- toll like receptor
- aqueous solution
- oxide nanoparticles
- transcription factor
- endoplasmic reticulum stress
- metal organic framework
- weight gain
- endothelial cells
- pi k akt
- cell death
- immune response
- mass spectrometry
- epithelial mesenchymal transition
- multidrug resistant
- small molecule
- gram negative
- protein protein