Methylmercury induces acute oxidative stress, altering Nrf2 protein level in primary microglial cells

Mingwei Ni, Xin Li, Zhaobao Yin, Haiyan Jiang, Marta Sidoryk-Wegrzynowicz, Dejan Milatovic, Jiyang Cai, Michael Aschner

Research output: Contribution to journalArticle

69 Citations (Scopus)

Abstract

The neurotoxicity of methylmercury (MeHg) is well documented in both humans and animals. MeHg causes acute and chronic damage to multiple organs, most profoundly the central nervous system (CNS). Microglial cells are derived from macrophage cell lineage, making up ~12% of cells in the CNS, yet their role in MeHg-induced neurotoxicity is not well defined. The purpose of the present study was to characterize microglial vulnerability to MeHg and their potential adaptive response to acute MeHg exposure. We examined the effects of MeHg on microglial viability, reactive oxygen species (ROS) generation, glutathione (GSH) level, redox homeostasis, and Nrf2 protein expression. Our data showed that MeHg (1-5μM) treatment caused a rapid (within 1 min) concentration and time-dependent increase in ROS generation, accompanied by a statistically significant decrease in the ratio of GSH and its oxidized form glutathione disulfide (GSSG) (GSH:GSSG ratio). MeHg increased the cytosolic Nrf2 protein level within 1 min of exposure, followed by its nuclear translocation after 10 min of treatment. Consistent with the nuclear translocation of Nrf2, quantitative real-time PCR revealed a concentration-dependent increase in the messenger RNA level of Ho-1, Nqo1, and xCT 30 min post MeHg exposure, whereas Nrf2 knockdown greatly reduced the upregulation of these genes. Furthermore, we observed increased microglial death upon Nrf2 knockdown by the small hairpin RNA approach. Taken together, our study has demonstrated that microglial cells are exquisitely sensitive to MeHg and respond rapidly to MeHg by upregulating the Nrf2-mediated antioxidant response.

Original languageEnglish (US)
Pages (from-to)590-603
Number of pages14
JournalToxicological Sciences
Volume116
Issue number2
DOIs
StatePublished - Apr 26 2010
Externally publishedYes

Fingerprint

Oxidative stress
Glutathione Disulfide
Neurology
Reactive Oxygen Species
Oxidative Stress
Macrophages
Central Nervous System
Small Interfering RNA
Glutathione
Animals
Proteins
Antioxidants
Genes
Cell Lineage
Messenger RNA
Oxidation-Reduction
Real-Time Polymerase Chain Reaction
Homeostasis
Up-Regulation

Keywords

  • Glutathione
  • Methylmercury
  • Microglial cells
  • Nrf2
  • Reactive oxygen species

ASJC Scopus subject areas

  • Toxicology
  • Medicine(all)

Cite this

Ni, M., Li, X., Yin, Z., Jiang, H., Sidoryk-Wegrzynowicz, M., Milatovic, D., ... Aschner, M. (2010). Methylmercury induces acute oxidative stress, altering Nrf2 protein level in primary microglial cells. Toxicological Sciences, 116(2), 590-603. https://doi.org/10.1093/toxsci/kfq126

Methylmercury induces acute oxidative stress, altering Nrf2 protein level in primary microglial cells. / Ni, Mingwei; Li, Xin; Yin, Zhaobao; Jiang, Haiyan; Sidoryk-Wegrzynowicz, Marta; Milatovic, Dejan; Cai, Jiyang; Aschner, Michael.

In: Toxicological Sciences, Vol. 116, No. 2, 26.04.2010, p. 590-603.

Research output: Contribution to journalArticle

Ni, M, Li, X, Yin, Z, Jiang, H, Sidoryk-Wegrzynowicz, M, Milatovic, D, Cai, J & Aschner, M 2010, 'Methylmercury induces acute oxidative stress, altering Nrf2 protein level in primary microglial cells', Toxicological Sciences, vol. 116, no. 2, pp. 590-603. https://doi.org/10.1093/toxsci/kfq126
Ni, Mingwei ; Li, Xin ; Yin, Zhaobao ; Jiang, Haiyan ; Sidoryk-Wegrzynowicz, Marta ; Milatovic, Dejan ; Cai, Jiyang ; Aschner, Michael. / Methylmercury induces acute oxidative stress, altering Nrf2 protein level in primary microglial cells. In: Toxicological Sciences. 2010 ; Vol. 116, No. 2. pp. 590-603.
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