Unfolded protein response in hypothalamic cultures of wild-type and ATF6α-knockout mice. (26th January 2016)
- Record Type:
- Journal Article
- Title:
- Unfolded protein response in hypothalamic cultures of wild-type and ATF6α-knockout mice. (26th January 2016)
- Main Title:
- Unfolded protein response in hypothalamic cultures of wild-type and ATF6α-knockout mice
- Authors:
- Lu, Wenjun
Hagiwara, Daisuke
Morishita, Yoshiaki
Tochiya, Masayoshi
Azuma, Yoshinori
Suga, Hidetaka
Goto, Motomitsu
Banno, Ryoichi
Sugimura, Yoshihisa
Oyadomari, Seiichi
Mori, Kazutoshi
Arima, Hiroshi - Abstract:
- Highlights: Thapsigargin (TG) activated all the UPR arms similarly in mouse hypothalamic cultures. TG-induced upregulation of BiP and CHOP was attenuated in ATF6α −/− mouse hypothalamus. TG-induced upregulation of ERAD components was also attenuated in ATF6α −/− mouse hypothalamus. Abstract: Recent studies suggest that endoplasmic reticulum (ER) stress in the hypothalamus could affect systemic homeostatic regulation in areas such as energy and water balance. Activating transcription factor 6α (ATF6α) is an ER stress transducer which increases the expression of ER chaperones and ER-associated degradation (ERAD) components under ER stress. In the present study, we examined the regulation of the unfolding protein response (UPR) in mouse hypothalamic cultures of wild-type (WT) and ATF6α −/− mice. Thapsigargin (TG), an ER stressor, significantly increased the mRNA expression of immunoglobulin heavy chain binding protein (BiP), spliced X-box binding protein 1 (XBP1), activating transcription factor 4 (ATF4), C/EBP homologous protein (CHOP), and ERAD components, in hypothalamic cultures of WT mice with the same threshold (0.1 μM) and similar time courses. On the other hand, TG-induced upregulation of BiP and CHOP as well as most ERAD-related genes, but not spliced XBP1 or ATF4, was attenuated in ATF6α −/− mice compared with WT mice. Our data suggest that all the UPR arms are activated similarly in the mouse hypothalamus under ER stress conditions, where ATF6α regulates theHighlights: Thapsigargin (TG) activated all the UPR arms similarly in mouse hypothalamic cultures. TG-induced upregulation of BiP and CHOP was attenuated in ATF6α −/− mouse hypothalamus. TG-induced upregulation of ERAD components was also attenuated in ATF6α −/− mouse hypothalamus. Abstract: Recent studies suggest that endoplasmic reticulum (ER) stress in the hypothalamus could affect systemic homeostatic regulation in areas such as energy and water balance. Activating transcription factor 6α (ATF6α) is an ER stress transducer which increases the expression of ER chaperones and ER-associated degradation (ERAD) components under ER stress. In the present study, we examined the regulation of the unfolding protein response (UPR) in mouse hypothalamic cultures of wild-type (WT) and ATF6α −/− mice. Thapsigargin (TG), an ER stressor, significantly increased the mRNA expression of immunoglobulin heavy chain binding protein (BiP), spliced X-box binding protein 1 (XBP1), activating transcription factor 4 (ATF4), C/EBP homologous protein (CHOP), and ERAD components, in hypothalamic cultures of WT mice with the same threshold (0.1 μM) and similar time courses. On the other hand, TG-induced upregulation of BiP and CHOP as well as most ERAD-related genes, but not spliced XBP1 or ATF4, was attenuated in ATF6α −/− mice compared with WT mice. Our data suggest that all the UPR arms are activated similarly in the mouse hypothalamus under ER stress conditions, where ATF6α regulates the expression of ER chaperones, CHOP, and ERAD components. … (more)
- Is Part Of:
- Neuroscience letters. Volume 612(2016)
- Journal:
- Neuroscience letters
- Issue:
- Volume 612(2016)
- Issue Display:
- Volume 612, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 612
- Issue:
- 2016
- Issue Sort Value:
- 2016-0612-2016-0000
- Page Start:
- 199
- Page End:
- 203
- Publication Date:
- 2016-01-26
- Subjects:
- ER endoplasmic reticulum -- UPR unfolded protein response -- IRE1 inositol requiring enzyme 1 -- PERK protein kinase RNA-like ER kinase -- ATF6α activating transcription factor 6α -- XBP1 X-box binding protein 1 -- eIF2α eukaryotic translation initiation factor 2α -- ATF4 activating transcription factor 4 -- CHOP C/EBP homologous protein -- BiP immunoglobulin heavy chain binding protein -- ERAD ER-associated degradation -- ERAC ER-associated compartment -- FNDI familial neurohypophysial diabetes insipidus -- TG thapsigargin -- EDEM1 ER degradation-enhancing α–mannosidase-like protein 1 -- MEF mouse embryonic fibroblast
Activating transcription factor 6α (ATF6α) -- Hypothalamus -- Endoplasmic reticulum (ER) stress -- Unfolded protein response (UPR) -- Endoplasmic reticulum-associated degradation (ERAD)
Neurology -- Periodicals
Neurology -- Periodicals
Research -- Periodicals
Neurologie -- Périodiques
Neuroanatomie -- Périodiques
Neuropharmacologie -- Périodiques
Neurophysiologie -- Périodiques
Neurology
Periodicals
Electronic journals
617.48 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03043940 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neulet.2015.12.031 ↗
- Languages:
- English
- ISSNs:
- 0304-3940
- Deposit Type:
- Legaldeposit
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