Literature DB >> 24895131

A novel suppressive effect of alcohol dehydrogenase 5 in neuronal differentiation.

Kaiyuan Wu1, Ruotong Ren1, Wenting Su1, Bo Wen1, Yuying Zhang1, Fei Yi2, Xinhua Qiao1, Tingting Yuan1, Jinhui Wang1, Limin Liu3, Juan Carlos Izpisua Belmonte4, Guang-Hui Liu5, Chang Chen6.   

Abstract

Alcohol dehydrogenase 5 (ADH5) is a conserved enzyme for alcohol and aldehyde metabolism in mammals. Despite dynamic expression throughout neurogenesis, its role in neuronal development remains unknown. Here we present the first evidence that ADH5 is a negative regulator of neuronal differentiation. Gene expression analyses identify a constant reduction of ADH5 levels throughout neuronal development. Overexpression of ADH5 reduces both development and adult neuronal differentiation of mouse neurons. This effect depends on the catalytic activity of ADH5 and involves ADH5-mediated denitrosation of histone deacetylase 2 (HDAC2). Our results indicate that ADH5 counteracts neuronal differentiation of human neural stem cells and that this effect can be reversed by pharmacological inhibition of ADH5. Based on these observations, we propose that ADH5 is a novel suppressor of neuronal differentiation and maturation. Inhibition of ADH5 may improve adult neurogenesis in a physiological or pathological setting.
© 2014 by The American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

Keywords:  Alcohol Dehydrogenase (ADH); Neural Stem Cell (NSC); Neurodifferentiation; Neurogenesis; S-Nitrosylation

Mesh:

Substances:

Year:  2014        PMID: 24895131      PMCID: PMC4106335          DOI: 10.1074/jbc.C114.561860

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  30 in total

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3.  Tissue- and species-specific expression patterns of class I, III, and IV Adh and Aldh 1 mRNAs in rodent embryos.

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4.  Lymphocyte development requires S-nitrosoglutathione reductase.

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5.  Characterization of green fluorescent protein-expressing retinal cells in CD 44-transgenic mice.

Authors:  V Sarthy; H Hoshi; S Mills; V J Dudley
Journal:  Neuroscience       Date:  2006-12-08       Impact factor: 3.590

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Authors:  J He; T Wang; P Wang; P Han; Q Yin; C Chen
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7.  SCFbeta-TRCP controls oncogenic transformation and neural differentiation through REST degradation.

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9.  The HDAC inhibitor, sodium butyrate, stimulates neurogenesis in the ischemic brain.

Authors:  Hyeon Ju Kim; Peter Leeds; De-Maw Chuang
Journal:  J Neurochem       Date:  2009-06-15       Impact factor: 5.372

10.  S-Nitrosylation of histone deacetylase 2 induces chromatin remodelling in neurons.

Authors:  Alexi Nott; P Marc Watson; James D Robinson; Luca Crepaldi; Antonella Riccio
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  9 in total

Review 1.  The role of S-nitrosoglutathione reductase (GSNOR) in human disease and therapy.

Authors:  Scott D Barnett; Iain L O Buxton
Journal:  Crit Rev Biochem Mol Biol       Date:  2017-04-10       Impact factor: 8.250

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3.  Increased GSNOR Expression during Aging Impairs Cognitive Function and Decreases S-Nitrosation of CaMKIIα.

Authors:  Yuying Zhang; Kaiyuan Wu; Wenting Su; Deng-Feng Zhang; Ping Wang; Xinhua Qiao; Qin Yao; Zengqiang Yuan; Yong-Gang Yao; Guanghui Liu; Chen Zhang; Limin Liu; Chang Chen
Journal:  J Neurosci       Date:  2017-09-07       Impact factor: 6.167

Review 4.  Modification of stem cell states by alcohol and acetaldehyde.

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Journal:  Chem Biol Interact       Date:  2019-12-14       Impact factor: 5.192

Review 5.  Formaldehyde and De/Methylation in Age-Related Cognitive Impairment.

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Review 6.  Current aging research in China.

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7.  TRPM7 maintains progenitor-like features of neuroblastoma cells: implications for metastasis formation.

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8.  Thallium stimulates ethanol production in immortalized hippocampal neurons.

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  9 in total

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