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Immunobiology. 2013 Apr;218(4):620-7. doi: 10.1016/j.imbio.2012.07.030. Epub 2012 Aug 4.

Altered redox state and apoptosis in the pathogenesis of systemic lupus erythematosus.

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1
Department of Dermatology, Massachusetts General Hospital (MGH), Harvard Medical School (HMS), Boston, MA, USA.

Abstract

An altered redox status and increased lymphocyte apoptosis have been implicated in the development of systemic lupus erythematosus (SLE). In this study, we evaluated the relationship between glutathione (GSH) depletion, reactive oxygen species (ROS) and, the progression of apoptosis and their association with SLE severity. Significant low levels of intracellular glutathione, total thiol and altered redox state (GSH/GSSG) were found in SLE patients, in which lymphocyte apoptosis and activated caspase-3 expression in the lymphocytes were remarkably increased. The severity of disease was positively allied with the increased levels of lymphocyte apoptosis and caspase-3, but negatively with the decreased levels of total thiol, depleted intracellular glutathione and altered redox state (GSH/GSSG). The lymphocyte apoptosis and activated caspase-3 expression were negatively associated with intracellular levels of GSH and redox state and positively associated with the elevated levels of multiple oxidative stress markers; ROS and lipid peroxidation measured as malondialdehyde (MDA). These results suggest that GSH depletion and elevated oxidative stress trigger apoptosis and may be coupled with the severity of the disease.

PMID:
22940256
DOI:
10.1016/j.imbio.2012.07.030
[Indexed for MEDLINE]
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