| Literature DB >> 35312958 |
Huidan Deng1,2, Song Zhu1,2, Huiru Yang1, Hengmin Cui3,4,5, Hongrui Guo6,7, Junliang Deng1,2, Zhihua Ren1, Yi Geng1, Ping Ouyang1, Zhiwen Xu1, Youtian Deng1, Yanqiu Zhu1.
Abstract
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.Entities:
Keywords: Copper; Inflammation; JAK-STAT pathway; MAPKs pathway; NF-κB pathway; NLRP3 inflammasome
Year: 2022 PMID: 35312958 DOI: 10.1007/s12011-022-03171-0
Source DB: PubMed Journal: Biol Trace Elem Res ISSN: 0163-4984 Impact factor: 3.738