Down-regulation of the amyloid protein precursor of Alzheimer's disease by antisense oligonucleotides reduces neuronal adhesion to specific substrata


Autoria(s): Coulson, EJ; Barrett, GL; Storey, E; Bartlett, PF; Beyreuther, K; Masters, CL
Data(s)

01/01/1997

Resumo

The hallmark of Alzheimer's disease is the cerebral deposition of amyloid which is derived from the amyloid precursor protein (APP). The function of APP is unknown but there is increasing evidence for the role of APP in cell-cell and/or cell-matrix interactions. Primary cultures of murine neurons were treated with antisense oligonucleotides to down-regulate APP. This paper presents evidence that APP mediates a substrate-specific interaction between neurons and extracellular matrix components collagen type I, laminin and heparan sulphate proteoglycan but not fibronectin or poly-L-lysine. It remains to be determined whether this effect is the direct result of APP-matrix interactions, or whether an intermediary pathway is involved. (C) 1997 Elsevier Science B.V.

Identificador

http://espace.library.uq.edu.au/view/UQ:57963

Idioma(s)

eng

Palavras-Chave #Neurosciences #Heparan Sulphate Proteoglycan #Collagen #Laminin #Fibronectin #Murine #Nerve Growth-factor #Heparan-sulfate Proteoglycan #Messenger-rna #Neurite Outgrowth #Cell-surface #Beta-protein #Extracellular-matrix #Differential Expression #Hippocampal-neurons #Cortical-neurons
Tipo

Journal Article