Subtoxic Doses of Cadmium Modulate Inflammatory Properties of Murine RAW 264.7 Macrophages

• Published in: BioMed research international 2015-01, Vol.2015 (2015), p.1-8
• Main Authors: Riemschneider, Sina, Lehmann, Jörg, Herzberg, Martin
• Format: Article
• Language: English
• Subjects: Animals; Antigens; Antigens, Bacterial - pharmacology; Bacterial infections; Cadmium; Cadmium - toxicity; Cell Line; Cell Survival - drug effects; Cell Survival - genetics; Chemokine CXCL1 - biosynthesis; Chemokines; Cytokines; Gene Expression Regulation - drug effects; Health aspects; Heavy metals; Humans; Immunomodulation - drug effects; Infections; Inflammation - chemically induced; Inflammation - genetics; Inflammation - pathology; Interleukin-10 - biosynthesis; Interleukin-1beta - biosynthesis; Interleukin-6 - biosynthesis; Interleukin-6 - metabolism; Ligands; Macrophages; Macrophages - drug effects; Macrophages - metabolism; Mass spectrometry; Mice; Nitric oxide; Nitric Oxide - metabolism; Reactive Oxygen Species - metabolism; Salmonella; Scientific imaging
• ISSN: 2314-6133; 2314-6141
• DOI: 10.1155/2015/295303

Cadmium (Cd) is a toxic heavy metal that exhibits various adverse effects in the human and animal organism. Its resemblance to essential metals such as calcium, iron, and zinc leads to an unintended uptake in cells after intake through inhalation and ingestion. In this study we investigated the toxicity and the immunomodulatory potential of Cd in nonactivated and activated murine macrophages (i.e., cell line RAW 264.7). Cadmium alone caused a dose-dependent decreased viability of exposed cells. Subtoxic Cd concentrations delayed cell death in macrophages, resulting from cytotoxic storm, producing reactive oxygen species (ROS) and nitric oxide (NO), in response to their stimulation by bacterial antigens via pattern-recognition receptors (PRRs). In addition, production of selected pro- and anti-inflammatory cytokines, the chemokine CXCL1 (KC), and NO was determined. We observed that proinflammatory IL-1β and also CXCL1 were highly upregulated whereas anti-inflammatory or regulatory cytokines IL-6 and IL-10 were suppressed by 10 µM Cd. Also production of antibacterial NO was significantly reduced through exposure to 10 µM Cd, maybe explaining better survival of macrophages. Additionally, we could show by analysis via ICP-MS that different effects of Cd in nonactivated and activated macrophages definitely did not result from different Cd uptake rates.