Uranyl nitrate-exposed rat alveolar macrophages cell death: Influence of superoxide anion and TNF α mediators
Creators
- 1. School of Science and Technology, National University of General Martín, Avda Gral Paz 5445 (1650) San Martín, Buenos Aires (Argentina)
- 2. School of Dentistry, University of Buenos Aires, M. T. de Alvear 2142 (1122), Buenos Aires (Argentina)
Description
Uranium compounds are widely used in the nuclear fuel cycle, military and many other diverse industrial processes. Health risks associated with uranium exposure include nephrotoxicity, cancer, respiratory, and immune disorders. Macrophages present in body tissues are the main cell type involved in the internalization of uranium particles. To better understand the pathological effects associated with depleted uranium (DU) inhalation, we examined the metabolic activity, phagocytosis, genotoxicity and inflammation on DU-exposed rat alveolar macrophages (12.5–200 μM). Stability and dissolution of DU could differ depending on the dissolvent and in turn alter its biological action. We dissolved DU in sodium bicarbonate (NaHCO3 100 mM) and in what we consider a more physiological vehicle resembling human internal media: sodium chloride (NaCl 0.9%). We demonstrate that uranyl nitrate in NaCl solubilizes, enters the cell, and elicits its cytotoxic effect similarly to when it is diluted in NaHCO3. We show that irrespective of the dissolvent employed, uranyl nitrate impairs cell metabolism, and at low doses induces both phagocytosis and generation of superoxide anion (O2−). At high doses it provokes the secretion of TNFα and through all the range of doses tested, apoptosis. We herein suggest that at DU low doses O2− may act as the principal mediator of DNA damage while at higher doses the signaling pathway mediated by O2− may be blocked, prevailing damage to DNA by the TNFα route. The study of macrophage functions after uranyl nitrate treatment could provide insights into the pathophysiology of uranium‐related diseases. -- Highlights: ► Uranyl nitrate effect on cultured macrophages is linked to the doses and independent of its solubility. ► At low doses uranyl nitrate induces generation of superoxide anion. ► At high doses uranyl nitrate provokes secretion of TNFα. ► Uranyl nitrate induces apoptosis through all the range of doses tested.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.taap.2012.04.022Additional details
Identifiers
- DOI
- 10.1016/j.taap.2012.04.022;
- PII
- S0041-008X(12)00158-5;
Publishing Information
- Journal Title
- Toxicology and Applied Pharmacology
- Journal Volume
- 261
- Journal Issue
- 3
- Journal Page Range
- p. 309-316
- ISSN
- 0041-008X
- CODEN
- TXAPA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45036304
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ANIMAL TISSUES; ANIONS; APOPTOSIS; DEPLETED URANIUM; DNA; DNA DAMAGES; DOSES; HEALTH HAZARDS; INFLAMMATION; INHALATION; MACROPHAGES; METABOLISM; NEOPLASMS; NUCLEAR FUELS; PHAGOCYTOSIS; RATS; SODIUM CARBONATES; SODIUM CHLORIDES; URANYL NITRATES
- Descriptors DEC
- ACTINIDE COMPOUNDS; ACTINIDES; ALKALI METAL COMPOUNDS; ANIMAL CELLS; ANIMALS; BODY; CARBON COMPOUNDS; CARBONATES; CHARGED PARTICLES; CHLORIDES; CHLORINE COMPOUNDS; CONNECTIVE TISSUE CELLS; DISEASES; ELEMENTS; ENERGY SOURCES; FUELS; HALIDES; HALOGEN COMPOUNDS; HAZARDS; INTAKE; IONS; MAMMALS; MATERIALS; METALS; NITRATES; NITROGEN COMPOUNDS; NUCLEIC ACIDS; ORGANIC COMPOUNDS; OXYGEN COMPOUNDS; PATHOLOGICAL CHANGES; PHAGOCYTES; REACTOR MATERIALS; RODENTS; SODIUM COMPOUNDS; SODIUM HALIDES; SOMATIC CELLS; SYMPTOMS; URANIUM; URANIUM COMPOUNDS; URANYL COMPOUNDS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.