Involvement of Prostaglandin E2 in Production of Amyloid-β Peptides Both in Vitro and in Vivo
| Autor: | Yukihiko Sugimoto, Shuh Narumiya, Ken Ichiro Tanaka, Toshiharu Suzuki, Tatsuya Hoshino, Masami Narita, Takashi Homan, Tohru Mizushima, Tadashi Nakaya, Wataru Araki |
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| Rok vydání: | 2007 |
| Předmět: |
medicine.medical_specialty
Prostaglandin E2 receptor EP4 Receptor Inflammation Stimulation Biology Biochemistry Dinoprostone Cell Line Mice Internal medicine Cyclic AMP medicine Animals Humans Receptors Prostaglandin E Phosphorylation Prostaglandin E2 Receptor Molecular Biology Mice Knockout Amyloid beta-Peptides HEK 293 cells P3 peptide Cell Biology Peptide Fragments Cell biology Enzyme Activation Endocrinology lipids (amino acids peptides and proteins) Amyloid Precursor Protein Secretases medicine.symptom medicine.drug |
| Zdroj: | Journal of Biological Chemistry. 282:32676-32688 |
| ISSN: | 0021-9258 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
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