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Involvement of prostaglandin E2 in production of amyloid-beta peptides both in vitro and in vivo.

Involvement of prostaglandin E2 in production of amyloid-beta peptides both in vitro and in vivo. Research Abstract Details 

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  • Involvement of prostaglandin E2 in production of amyloid-beta peptides both in vitro and in vivo. Abstract Text:

    tatsuya hoshinoTatsuya Hoshino,tadashi nakayaTadashi Nakaya,takashi homanTakashi Homan,ken-ichiro tanakaKen-ichiro Tanaka,yukihiko sugimotoYukihiko Sugimoto,wataru arakiWataru Araki,masami naritaMasami Narita,shuh narumiyaShuh Narumiya,toshiharu suzukiToshiharu Suzuki,tohru mizushimaTohru Mizushima,tatsuya hoshinoTatsuya Hoshino,tadashi nakayaTadashi Nakaya,takashi homanTakashi Homan,ken-ichiro tanakaKen-ichiro Tanaka,yukihiko sugimotoYukihiko Sugimoto,wataru arakiWataru Araki,masami naritaMasami Narita,shuh narumiyaShuh Narumiya,toshiharu suzukiToshiharu Suzuki,tohru mizushimaTohru Mizushima,

    Amyloid-beta peptides (Abeta), generated by proteolysis of the beta-amyloid precursor protein (APP) by beta- and gamma-secretases, play an important role in the pathogenesis of Alzheimer disease (AD). Inflammation is also believed to be integral to the pathogenesis of AD. Here we show that prostaglandin E(2) (PGE(2)), a strong inducer of inflammation, stimulates the production of Abeta in cultured human embryonic kidney (HEK) 293 or human neuroblastoma (SH-SY5Y) cells, both of which express a mutant type of APP. We have demonstrated using subtype-specific agonists that, of the four main subtypes of PGE(2) receptors (EP(1-4)), EP(4) receptors alone or EP(2) and EP(4) receptors together are responsible for this PGE(2)-stimulated production of Abeta in HEK293 or SH-SY5Y cells, respectively. An EP(4) receptor antagonist suppressed the PGE(2)-stimulated production of Abeta in HEK293 cells. This stimulation was accompanied by an increase in cellular cAMP levels, and an analogue of cAMP stimulated the production of Abeta, demonstrating that increases in the cellular level of cAMP are responsible for the PGE(2)-stimulated production of Abeta. Immunoblotting experiments and direct measurement of gamma-secretase activity suggested that PGE(2)-stimulated production of Abeta is mediated by activation ofgamma-secretase but not of beta-secretase. Transgenic mice expressing the mutant type of APP showed lower levels of Abeta in the brain, when they were crossed with mice lacking either EP(2) or EP(4) receptors, suggesting that PGE(2)-mediated activation of EP(2) and EP(4) receptors is involved in the production of Abeta in vivo and in the pathogenesis of AD.

    Involvement of prostaglandin E2 in production of amyloid-beta peptides both in vitro and in vivo. Publishing Authors By Initials

    t hoshinoT Hoshino,t nakayaT Nakaya,t homanT Homan,k tanakaK Tanaka,y sugimotoY Sugimoto,w arakiW Araki,m naritaM Narita,s narumiyaS Narumiya,t suzukiT Suzuki,t mizushimaT Mizushima,t hoshinoT Hoshino,t nakayaT Nakaya,t homanT Homan,k tanakaK Tanaka,y sugimotoY Sugimoto,w arakiW Araki,m naritaM Narita,s narumiyaS Narumiya,t suzukiT Suzuki,t mizushimaT Mizushima,

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    Involvement of prostaglandin E2 in production of amyloid-beta peptides both in vitro and in vivo. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: The Journal of biological chemistry

    VOLUME: 282

    Page Numbers: 32676-88

    Journal Abbreviation: J. Biol. Chem.

    ISSN: 0021-9258

    DAY: 2

    MONTH: 09

    YEAR: 2007

    Involvement of prostaglandin E2 in production of amyloid-beta peptides both in vitro and in vivo. Information

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    LANGUAGE: eng

    NlmUniqueID: 2985121

    Involvement of prostaglandin E2 in production of amyloid-beta peptides both in vitro and in vivo. Keywords Mesh Terms:

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    Grant and Affiliation Information for Involvement of prostaglandin E2 in production of amyloid-beta peptides both in vitro and in vivo.

    AFFILIATION: Graduate School of Medical and Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto 862-0973, Japan.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Biol Chem

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