Title : Copper chelators promote nonamyloidogenic processing of AβPP via MT1/2 /CREB-dependent signaling pathways in AβPP/PS1 transgenic mice.

Pub. Date : 2018 Oct

PMID : 29710396






4 Functional Relationships(s)
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1 Second, TM and another copper chelator, bathocuproine sulfonate (BCS), promoted nonamyloidogenic processing of AbetaPP via inducing the expression of ADAM10 and the secretion of sAbetaPPalpha. Copper a disintegrin and metallopeptidase domain 10 Mus musculus
2 Third, the inducible ADAM10 production caused by copper chelators can be blocked by a melatonin receptor (MT1/2 ) antagonist (luzindole) and a MT2 inhibitor (4-P-PDOT), suggesting that the expression of ADAM10 depends on the activation of MT1/2 signaling pathways. Copper a disintegrin and metallopeptidase domain 10 Mus musculus
3 Third, the inducible ADAM10 production caused by copper chelators can be blocked by a melatonin receptor (MT1/2 ) antagonist (luzindole) and a MT2 inhibitor (4-P-PDOT), suggesting that the expression of ADAM10 depends on the activation of MT1/2 signaling pathways. Copper a disintegrin and metallopeptidase domain 10 Mus musculus
4 Based on these results, we conclude that copper chelators regulate the balance between amyloidogenic and nonamyloidogenic processing of AbetaPP via promoting ADAM10 expression through MT1/2 /CREB-dependent signaling pathways. Copper a disintegrin and metallopeptidase domain 10 Mus musculus