4.7 Article

c-Jun-dependent sulfiredoxin induction mediates BDNF protection against mitochondrial inhibition in rat cortical neurons

Journal

NEUROBIOLOGY OF DISEASE
Volume 46, Issue 2, Pages 450-462

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2012.02.010

Keywords

Akt; ERK1/2; JNK; Neuroprotection; PI3-K; Primary cortical neurons; siRNA

Categories

Funding

  1. National Science Council of Taiwan [NSC97-2314-B-010-008MY3, NSC98-2314-B-010-020MY3]
  2. Ministry of Education of Taiwan [95A-C-P30, 99A-C-B6, 100A-C-B5]
  3. Department of Health of Taipei City Government [10001-62-025]
  4. Chang Gung Memorial Hospital [CMRPG880801, CMRPG880802]
  5. Cheng Hsin General Hospital [100F117CY17, 100-13]

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In current study, we tested the hypothesis that c-Jun-dependent sulfiredoxin expression mediates protective effects of brain-derived neurotrophic factor (BDNF) against neurotoxicity induced by 3-nitropropionic acid (3-NP), a mitochondrial complex II inhibitor, in primary rat cortical cultures. We found that BDNF-dependent c-Jun expression and nuclear translocation required prior phosphorylation of extracellular signal-regulated kinase (ERK)1/2, but not Akt. BDNF also transiently activated the expression of sulfiredoxin, an ATP-dependent antioxidant enzyme, at both mRNA and protein levels. Furthermore, both c-Jun siRNA and ERK1/2 inhibitor PD98059 suppressed BDNF-induced sulfiredoxin expression. Finally, PD98059, c-Jun siRNA, and sulfiredoxin siRNA all abrogated BDNF-mediated 3-NP resistance. Together, these results established a signaling cascade of BDNF -> ERK1/2-Pi -> c-Jun -> sulfiredoxin -> 3-NP resistance. We therefore conclude that c-Jun-induced sulfiredoxin mediates the BDNF-dependent neuroprotective effects against 3-NP toxicity in primary rat cortical neurons, at least in part. (C) 2012 Elsevier Inc. All rights reserved.

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