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Search: WFRF:(Sandberg Mats 1953) > (2010-2014) > The Nrf2-inducible ...

The Nrf2-inducible antioxidant defense in astrocytes can be both up- and down-regulated by activated microglia:Involvement of p38 MAPK.

Correa, Fernando (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi,Institute of Biomedicine, Department of Medical Biochemistry and Cell Biology
Ljunggren, Elin (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för farmakologi,Institute of Neuroscience and Physiology, Department of Pharmacology
Mallard, Carina, 1963 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology
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Nilsson, Michael, 1962 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för klinisk neurovetenskap och rehabilitering,Institute of Neuroscience and Physiology, Department of Clinical Neuroscience and Rehabilitation
Weber, Stephen G (author)
Sandberg, Mats, 1953 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi,Institute of Biomedicine, Department of Medical Biochemistry and Cell Biology
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 (creator_code:org_t)
2011-02-23
2011
English.
In: Glia. - : Wiley. - 1098-1136 .- 0894-1491. ; 59:5, s. 785-99
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The effects of microglia-conditioned medium (MCM) on the inducible Nrf2 system in astrocyte-rich cultures were investigated by determination of glutathione (GSH) levels, γglutamylcysteine ligase (γGCL) activity, the protein levels of Nrf2, Keap1, the modulatory subunit of γGCL (γGCL-M) and activated MAP kinases (ERK1/2, JNK and p38). Microglia were either cultured for 24 h in serum-free culture medium to achieve microglia-conditioned medium from non-activated cells (MCM(0) ), used as control condition, or activated with different concentrations (0.1-1,000 ng mL(-1) ) of lipopolysaccharide (LPS) to produce MCM(0.1-1,000) . Acute exposure (24 h) to MCM(100) increased GSH, γGCL activity, the protein levels of γGCL-M, Nrf2, and activated JNK and ERK1/2 in astrocyte-rich cultures. In contrast, treatment with MCM(10) for 24 h decreased components of the Nrf2 system in parallel with activation of p38 MAPK. Stimulation of the Nrf2 system by tBHQ was partly intact after 24 h but blocked after 72 h treatment with MCM(10) and MCM(100) . This down-regulation after 72 h correlated with activation of p38 MAPK and lack of ERK1/2 and JNK activation. The negative effects were partly reversed by an inhibitor of p38 which restored tBHQ mediated protection against oxidative stress. In conclusion, the study showed a negative effect of MCM(10) on the inducible anti-oxidant defense in astrocyte-rich cultures at both 24 and 72 h that correlated with activation of p38 and was partly reversed by a p38 inhibitor. A transient protective effect of MCM(100) on astrocyte-rich cultures against H(2)O(2) toxicity was observed at 24 h which coincided with activation of JNK and ERK1/2.

Keyword

Analysis of Variance
Animals
Animals
Newborn
Astrocytes
cytology
drug effects
immunology
metabolism
Blotting
Western
Cell Survival
physiology
Cells
Cultured
Cerebral Cortex
cytology
drug effects
metabolism
Culture Media
Conditioned
Down-Regulation
drug effects
physiology
Extracellular Signal-Regulated MAP Kinases
metabolism
Glutathione
metabolism
Hydroquinones
pharmacology
JNK Mitogen-Activated Protein Kinases
metabolism
Microglia
cytology
drug effects
immunology
metabolism
NF-E2-Related Factor 2
metabolism
Oxidative Stress
drug effects
physiology
Rats
Rats
Sprague-Dawley
Up-Regulation
drug effects
physiology
p38 Mitogen-Activated Protein Kinases
metabolism

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