Premium
Impact of endogenous nitric oxide on microglial cell energy metabolism and labile iron pool
Author(s) -
Chénais Benoît,
Morjani Hamid,
Drapier JeanClaude
Publication year - 2002
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.2002.00864.x
Subject(s) - nitric oxide , microglia , endogeny , biochemistry , microbiology and biotechnology , cellular respiration , lipopolysaccharide , respiratory chain , digitonin , chemistry , metabolism , respiration , bioenergetics , mitochondrion , biology , inflammation , enzyme , immunology , endocrinology , botany
Microglial activation is common in several neurodegenerative disorders. In the present study, we used the murine BV‐2 microglial cell line stimulated with γ‐interferon and lipopolysaccharide to gain new insights into the effects of endogenously produced NO on mitochondrial respiratory capacity, iron regulatory protein activity, and redox‐active iron level. Using polarographic measurement of respiration of both intact and digitonin‐permeabilized cells, and spectrophotometric determination of individual respiratory chain complex activity, we showed that in addition to the reversible inhibition of cytochrome‐c oxidase, long‐term endogenous NO production reduced complex‐I and complex‐II activities in an irreversible manner. As a consequence, the cellular ATP level was decreased in NO‐producing cells, whereas ATPase activity was unaffected. We show that NO up‐regulates RNA‐binding of iron regulatory protein 1 in microglial cells, and strongly reduces the labile iron pool. Together these results point to a contribution of NO derived from inflammatory microglia to the misregulation of energy‐producing reactions and iron metabolism, often associated with the pathogenesis of neurodegenerative disorders.