Literature DB >> 32165495

A peroxisome deficiency-induced reductive cytosol state up-regulates the brain-derived neurotrophic factor pathway.

Yuichi Abe1, Masanori Honsho2, Ryoko Kawaguchi3, Takashi Matsuzaki4, Yayoi Ichiki5, Masashi Fujitani6, Kazushirou Fujiwara3, Masaaki Hirokane3, Masahide Oku5, Yasuyoshi Sakai5, Toshihide Yamashita7, Yukio Fujiki8.   

Abstract

The peroxisome is a subcellular organelle that functions in essential metabolic pathways, including biosynthesis of plasmalogens, fatty acid β-oxidation of very-long-chain fatty acids, and degradation of hydrogen peroxide. Peroxisome biogenesis disorders (PBDs) manifest as severe dysfunction in multiple organs, including the central nervous system (CNS), but the pathogenic mechanisms in PBDs are largely unknown. Because CNS integrity is coordinately established and maintained by neural cell interactions, we here investigated whether cell-cell communication is impaired and responsible for the neurological defects associated with PBDs. Results from a noncontact co-culture system consisting of primary hippocampal neurons with glial cells revealed that a peroxisome-deficient astrocytic cell line secretes increased levels of brain-derived neurotrophic factor (BDNF), resulting in axonal branching of the neurons. Of note, the BDNF expression in astrocytes was not affected by defects in plasmalogen biosynthesis and peroxisomal fatty acid β-oxidation in the astrocytes. Instead, we found that cytosolic reductive states caused by a mislocalized catalase in the peroxisome-deficient cells induce the elevation in BDNF secretion. Our results suggest that peroxisome deficiency dysregulates neuronal axogenesis by causing a cytosolic reductive state in astrocytes. We conclude that astrocytic peroxisomes regulate BDNF expression and thereby support neuronal integrity and function.
© 2020 Abe et al.

Entities:  

Keywords:  GSH; astrocyte; axon branching; brain-derived neurotrophic factor (BDNF); catalase; glia; glial cell; neurodegeneration; nicotinamide adenine dinucleotide (NADH); peroxisome biogenesis disorder (PBD); plasmalogen

Mesh:

Substances:

Year:  2020        PMID: 32165495      PMCID: PMC7170515          DOI: 10.1074/jbc.RA119.011989

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


  67 in total

1.  Two proteases, trypsin domain-containing 1 (Tysnd1) and peroxisomal lon protease (PsLon), cooperatively regulate fatty acid β-oxidation in peroxisomal matrix.

Authors:  Kanji Okumoto; Yukari Kametani; Yukio Fujiki
Journal:  J Biol Chem       Date:  2011-10-14       Impact factor: 5.157

2.  Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.

Authors:  S Tamura; N Matsumoto; A Imamura; N Shimozawa; Y Suzuki; N Kondo; Y Fujiki
Journal:  Biochem J       Date:  2001-07-15       Impact factor: 3.857

3.  Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency.

Authors:  Yuichi Abe; Masanori Honsho; Hiroki Nakanishi; Ryo Taguchi; Yukio Fujiki
Journal:  Biochim Biophys Acta       Date:  2014-01-10

4.  Tissue fractionation studies. 17. Intracellular distribution of monoamine oxidase, aspartate aminotransferase, alanine aminotransferase, D-amino acid oxidase and catalase in rat-liver tissue.

Authors:  P Baudhuin; H Beaufay; Y Rahman-Li; O Z Sellinger; R Wattiaux; P Jacques; C De Duve
Journal:  Biochem J       Date:  1964-07       Impact factor: 3.857

5.  The peroxin Pex14p. cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysis.

Authors:  N Shimizu; R Itoh; Y Hirono; H Otera; K Ghaedi; K Tateishi; S Tamura; K Okumoto; T Harano; S Mukai; Y Fujiki
Journal:  J Biol Chem       Date:  1999-04-30       Impact factor: 5.157

6.  Functional domains and dynamic assembly of the peroxin Pex14p, the entry site of matrix proteins.

Authors:  Ryota Itoh; Yukio Fujiki
Journal:  J Biol Chem       Date:  2006-02-02       Impact factor: 5.157

7.  A novel fluorescent sensor protein for visualization of redox states in the cytoplasm and in peroxisomes.

Authors:  Taisuke Yano; Masahide Oku; Natsuko Akeyama; Akinori Itoyama; Hiroya Yurimoto; Shusuke Kuge; Yukio Fujiki; Yasuyoshi Sakai
Journal:  Mol Cell Biol       Date:  2010-05-24       Impact factor: 4.272

8.  Multiple promoters direct stimulus and temporal specific expression of brain-derived neurotrophic factor in the somatosensory cortex.

Authors:  S Nanda; K J Mack
Journal:  Brain Res Mol Brain Res       Date:  1998-11-20

9.  Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder.

Authors:  P L Faust; M E Hatten
Journal:  J Cell Biol       Date:  1997-12-01       Impact factor: 10.539

10.  The VDAC2-BAK axis regulates peroxisomal membrane permeability.

Authors:  Ken-Ichiro Hosoi; Non Miyata; Satoru Mukai; Satomi Furuki; Kanji Okumoto; Emily H Cheng; Yukio Fujiki
Journal:  J Cell Biol       Date:  2017-02-07       Impact factor: 10.539

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  3 in total

Review 1.  Recent progresses in novel in vitro models of primary neurons: A biomaterial perspective.

Authors:  Jiangang Zhang; Huiyu Yang; Jiaming Wu; Dingyue Zhang; Yu Wang; Jiliang Zhai
Journal:  Front Bioeng Biotechnol       Date:  2022-08-17

Review 2.  Dysfunctional peroxisomal lipid metabolisms and their ocular manifestations.

Authors:  Chuck T Chen; Zhuo Shao; Zhongjie Fu
Journal:  Front Cell Dev Biol       Date:  2022-09-07

3.  The peroxisome counteracts oxidative stresses by suppressing catalase import via Pex14 phosphorylation.

Authors:  Kanji Okumoto; Mahmoud El Shermely; Masanao Natsui; Hidetaka Kosako; Ryuichi Natsuyama; Toshihiro Marutani; Yukio Fujiki
Journal:  Elife       Date:  2020-08-24       Impact factor: 8.140

  3 in total

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