4.4 Article

ER and Golgi stresses increase ER-Golgi SNARE Syntaxin5: Implications for organelle stress and βAPP processing

Journal

NEUROSCIENCE LETTERS
Volume 604, Issue -, Pages 30-35

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2015.07.017

Keywords

ER stress; Golgi stress; Hippocampus; Neuron; SNARE; Syntaxin5

Categories

Funding

  1. Japan Society for the Promotion of Science [24300142, 19500327, 25430072, 24500462]
  2. Promotion and Mutual Aid Cooperation Program for Private Schools in Japan
  3. Kyorin University School of Medicine
  4. Grants-in-Aid for Scientific Research [25430072, 19500327, 24500462] Funding Source: KAKEN

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Unresolved endoplasmic reticulum (ER) stress causes neuronal death and has been implicated in neurodegenerative conditions such as Alzheimer's disease (AD). However, the mechanisms by which stress signals propagate from the ER through the Golgi apparatus and their effects on the transport and processing of AD-related proteins, such as beta-amyloid precursor protein (beta APP), are unknown. We recently found that in the NG108-15 cell line, ER stress upregulates ER-Golgi-soluble N-ethylmaleimide-sensitive factor-attachment protein receptors (ER-Golgi SNAREs) Syx5 and Bet1. In the present study, we examined the effects of apoptosis and ER stress inducers on the expression of ER Golgi SNARE proteins and cell viability in a primary culture of rat hippocampal neurons. An apoptosis inducer significantly downregulated the expression of ER Golgi SNARE Syx5. ER-stress inducers upregulated the expression of Syx5 isoforms and Bet1 proteins via de novo synthesis of their mRNA transcripts. Knockdown of Syx5 during apoptosis or ER stress induction enhanced vulnerability of neurons. Additionally, we examined the effects of Golgi stress on Syx5 expression and PAPP processing. Golgi stress also induced upregulation of ER Golgi SNARE Syx5, and concomitantly, suppressed amyloid-beta peptide secretion. These findings suggest that Syx5 is a potential stress responsive factor that participates in beta APP processing and the survival pathways of neuronal cells. (C) 2015 Elsevier Ireland Ltd. All rights reserved.

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