Literature DB >> 12485401

Region-specific and epileptogenic-dependent expression of six subtypes of alpha2,3-sialyltransferase in the adult mouse brain.

Hitomi Matsuhashi1, Yoichiro Horii, Keiko Kato.   

Abstract

Sialylated glycoconjugates play important roles in various biological functions. The structures are also observed in brains and it has been proposed that sialylation may affect neural plasticity. To clarify the effects of sialylation in the brain, particular neurons that exhibit sialylation should first be determined. Using in situ hybridization, we performed systematic surveys of the localization of mRNAs encoding the six alpha2,3-sialyltransferases (ST3Gal I-VI) in the adult mouse brain with or without physiological stimulation. First, striking region-specific patterns of expression were observed: While ST3Gal II, III, and V mRNAs were in neuronal cells throughout the brain, ST3Gal I, IV, and VI mRNAs were in restricted brain regions. Next, to assess whether the expression of the six mRNAs can be regulated, we examined the effect of kindling epileptogenesis on the six mRNA levels. Of the six subtypes, upregulation in the ST3Gal IV level in the thalamus was most pronounced; the number of ST3Gal IV-expressing neurons in the anterior thalamic nuclei increased from 2% to 21% in a time-dependent manner during epileptogenesis. Western blot analysis evaluated the increase of the end-products in the thalamus. These findings provide a molecular basis to clarify when and where sialylated glycoconjugates function accompanied by neural plasticity.

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Year:  2003        PMID: 12485401     DOI: 10.1046/j.1471-4159.2003.01257.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.372


  6 in total

1.  Sialylation regulates brain structure and function.

Authors:  Seung-Wan Yoo; Mary G Motari; Keiichiro Susuki; Jillian Prendergast; Andrea Mountney; Andres Hurtado; Ronald L Schnaar
Journal:  FASEB J       Date:  2015-04-06       Impact factor: 5.191

2.  Reduced expression of the μ opioid receptor in some, but not all, brain regions in mice with OPRM1 A112G.

Authors:  Y-J Wang; P Huang; A Ung; J A Blendy; L-Y Liu-Chen
Journal:  Neuroscience       Date:  2012-01-03       Impact factor: 3.590

3.  A common single nucleotide polymorphism A118G of the μ opioid receptor alters its N-glycosylation and protein stability.

Authors:  Peng Huang; Chongguang Chen; Stephen D Mague; Julie A Blendy; Lee-Yuan Liu-Chen
Journal:  Biochem J       Date:  2012-01-01       Impact factor: 3.857

4.  Differential effects of dietary oils on emotional and cognitive behaviors.

Authors:  Keiko Kato
Journal:  PLoS One       Date:  2015-03-23       Impact factor: 3.240

Review 5.  Knock-In Mouse Models to Investigate the Functions of Opioid Receptors in vivo.

Authors:  Jade Degrandmaison; Samuel Rochon-Haché; Jean-Luc Parent; Louis Gendron
Journal:  Front Cell Neurosci       Date:  2022-01-31       Impact factor: 5.505

6.  Urinary volatilome analysis in a mouse model of anxiety and depression.

Authors:  Akiko Fujita; Takaya Okuno; Mika Oda; Keiko Kato
Journal:  PLoS One       Date:  2020-02-21       Impact factor: 3.240

  6 in total

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