Literature DB >> 8635535

Specific toxicity of tunicamycin in induction of programmed cell death of sympathetic neurons.

J Y Chang1, V V Korolev.   

Abstract

Tunicamycin belongs to a group of antibiotics which can cause severe a nd often fatal neurological malfunction in animals, commonly known as "annual ryegrass toxicity." At the cellular level, tunicamycin is a potent glycosylation inhibitor which is often used to elucidate the importance of glycosylation in protein functions. Earlier reports suggested that tunicamycin was able to interfere with the binding of nerve growth factor to its receptors. In this report, we showed that tunicamycin was able to kill sympathetic neurons in cultures. The mechanism of cell death was observed to be similar to that of "programmed cell death" in sympathetic neurons induced by nerve growth factor deprivation. Such tunicamycin-induced cell death could be prevented by the protein synthesis inhibitor cycloheximide, which was known to prevent the programmed cell death in sympathetic neurons. These results demonstrated that, in addition to the proven CNS neurotoxicity in animals, tunicamycin causes programmed cell death in peripheral (sympathetic) neurons.

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Year:  1996        PMID: 8635535     DOI: 10.1006/exnr.1996.0019

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  7 in total

1.  Activity-dependent augmentation of spontaneous neurotransmission during endoplasmic reticulum stress.

Authors:  Elena Nosyreva; Ege T Kavalali
Journal:  J Neurosci       Date:  2010-05-26       Impact factor: 6.167

2.  Morphological and biochemical changes during programmed cell death of rat cerebellar granule cells.

Authors:  J Y Chang; J Z Wang
Journal:  Neurochem Res       Date:  1997-01       Impact factor: 3.996

3.  CHOP is implicated in programmed cell death in response to impaired function of the endoplasmic reticulum.

Authors:  H Zinszner; M Kuroda; X Wang; N Batchvarova; R T Lightfoot; H Remotti; J L Stevens; D Ron
Journal:  Genes Dev       Date:  1998-04-01       Impact factor: 11.361

4.  Protection from ataxia-linked apoptosis by gap junction inhibitors.

Authors:  Dingbo Lin; Dolores J Takemoto
Journal:  Biochem Biophys Res Commun       Date:  2007-08-27       Impact factor: 3.575

5.  Tunicamycin-induced cell death in the trigeminal ganglion is suppressed by nerve growth factor in the mouse embryo.

Authors:  Hiroyuki Ichikawa; Bing-Ran Zhao; Mitsuhiro Kano; Yoshinaka Shimizu; Toshihiko Suzuki; Ruji Terayama; Saburo Matsuo; Tomosada Sugimoto
Journal:  Cell Mol Neurobiol       Date:  2009-10-17       Impact factor: 5.046

6.  Identification of novel stress-induced genes downstream of chop.

Authors:  X Z Wang; M Kuroda; J Sok; N Batchvarova; R Kimmel; P Chung; H Zinszner; D Ron
Journal:  EMBO J       Date:  1998-07-01       Impact factor: 11.598

Review 7.  Role of endoplasmic reticulum stress in drug-induced toxicity.

Authors:  Fabienne Foufelle; Bernard Fromenty
Journal:  Pharmacol Res Perspect       Date:  2016-02-04
  7 in total

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