Chronic early childhood exposure to arsenic is associated with a TNF-mediated proteomic signaling response

Lisa Smeester, Paige A. Bommarito, Elizabeth M. Martin, Rogelio Recio-Vega, Tania Gonzalez-Cortes, Edgar Olivas-Calderon, R. Clark Lantz, Rebecca C. Fry

Research output: Contribution to journalArticle

7 Scopus citations

Abstract

Exposure to inorganic arsenic (iAs) in drinking water is a global public health concern and is associated with a range of health outcomes, including immune dysfunction. Children are a particularly sensitive population to the effects of inorganic arsenic, yet the biological mechanisms underlying adverse health outcomes are understudied. Here we used a proteomic approach to examine the effects of iAs exposure on circulating serum protein levels in a cross-sectional children's cohort in Mexico. To identify iAs-associated proteins, levels of total urinary arsenic (U-tAs) and its metabolites were determined and serum proteins assessed for differences in expression. The results indicate an enrichment of Tumor Necrosis Factor-(TNF)-regulated immune and inflammatory response proteins that displayed decreased expression levels in relation to increasing U-tAs. Notably, when analyzed in the context of the proportions of urinary arsenic metabolites in children, the most robust response was observed in relation to the monomethylated arsenicals. This study is among the first serum proteomics assessment in children exposed to iAs.

Original languageEnglish (US)
Pages (from-to)183-187
Number of pages5
JournalEnvironmental Toxicology and Pharmacology
Volume52
DOIs
StatePublished - Jun 1 2017

Keywords

  • Arsenic
  • Arsenic metabolism
  • Early childhood exposure
  • Proteomics

ASJC Scopus subject areas

  • Toxicology
  • Pharmacology
  • Health, Toxicology and Mutagenesis

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    Smeester, L., Bommarito, P. A., Martin, E. M., Recio-Vega, R., Gonzalez-Cortes, T., Olivas-Calderon, E., Lantz, R. C., & Fry, R. C. (2017). Chronic early childhood exposure to arsenic is associated with a TNF-mediated proteomic signaling response. Environmental Toxicology and Pharmacology, 52, 183-187. https://doi.org/10.1016/j.etap.2017.04.007