Abstract
Taurine chloramine (TauCl) is produced from taurine by the myeloperoxidase-halide system in activated neutrophils via a stoichiometric reaction between taurine and HOCl. TauCl has been shown to provide cytoprotection against inflammatory tissue injury by inhibiting the overproduction of inflammatory mediators and also by increasing the expression of antioxidant enzymes that are regulated by nuclear factor E2-related factor 2 in murine macrophages. In this study, primary murine macrophages were prepared after either by injection of 3% thioglycolate into mouse peritoneal cavity or by differentiation of the isolated bone marrow cells. TauCl increased HO-1, Prx-1, and Trx-1 expression in murine primary macrophages. Also, when TauCl was injected in combination with 3% thioglycolate, HO-1 expression in the peritoneal macrophages was increased. Our results suggest that TauCl plays a protective role against cytotoxicity of oxidative stress in macrophages by increasing the expression of antioxidant enzymes in vivo.
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Abbreviations
- ARE:
-
Antioxidant response element
- BMDM:
-
Bone marrow-derived macrophages
- GPx:
-
Glutathione peroxidase
- HO:
-
Heme oxygenase
- Keap:
-
Kelch-like ECH-associated protein
- LPS:
-
Lipopolysaccharide
- M-CSF:
-
Macrophage colony stimulating factor
- MMP:
-
Metalloproteinase
- MPO:
-
Myeloperoxidase
- Nrf2:
-
Nuclear factor E2-related factor
- Prx:
-
Peroxiredoxin
- TauCl:
-
Taurine chloramine
- TNF-α:
-
Tumor necrosis factor-α
- Trx:
-
Thioredoxin
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Acknowledgments
We thank Dr. Young-Nam Cha for discussions throughout the study and critical comments on the manuscript, and Mi Ran Cho for the technical support. This work was supported by the NRF of Korea grant funded by the Korea government MEST (2012R1A1A3007097) and Inha University research grant.
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Kang, I.S., Kim, C. (2013). Taurine Chloramine Administered In Vivo Increases NRF2-Regulated Antioxidant Enzyme Expression in Murine Peritoneal Macrophages. In: El Idrissi, A., L'Amoreaux, W. (eds) Taurine 8. Advances in Experimental Medicine and Biology, vol 775. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-6130-2_22
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DOI: https://doi.org/10.1007/978-1-4614-6130-2_22
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