| Literature DB >> 29545881 |
Li Xue1,2, Yan Geng2, Ming Li3, Yao-Feng Jin4, Hui-Xun Ren1, Xia Li5, Feng Wu6, Biao Wang1, Wei-Ying Cheng1, Teng Chen7, Yan-Jiong Chen1.
Abstract
Previous studies have demonstrated that methamphetamine (MA) influences host immunity; however, the effect of MA on lipopolysaccharide (LPS)-induced immune responses remains unknown. Mast cells (MCs) are considered to serve an important role in the innate and acquired immune response, but it remains unknown whether MA modulates MC activation and LPS-stimulated cytokine production. The present study aimed to investigate the effect of MA on LPS-induced MC activation and the production of MC-derived cytokines in mice. Markers for MC activation, including cluster of differentiation 117 and the type I high affinity immunoglobulin E receptor, were assessed in mouse intestines. Levels of MC-derived cytokines in the lungs and thymus were also examined. The results demonstrated that cytokines were produced in the bone marrow-derived mast cells (BMMCs) of mice. The present study demonstrated that MA suppressed the LPS-mediated MC activation in mouse intestines. MA also altered the release of MC cytokines in the lung and thymus following LPS stimulation. In addition, LPS-stimulated cytokines were decreased in the BMMCs of mice following treatment with MA. The present study demonstrated that MA may regulate LPS-stimulated MC activation and cytokine production.Entities:
Keywords: chemokines; cytokines; lipopolysaccharide; mast cell; methamphetamine
Year: 2018 PMID: 29545881 PMCID: PMC5841010 DOI: 10.3892/etm.2018.5837
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447