Literature DB >> 10366748

The Alzheimer-related gene presenilin 1 facilitates notch 1 in primary mammalian neurons.

O Berezovska1, M Frosch, P McLean, R Knowles, E Koo, D Kang, J Shen, F M Lu, S E Lux, S Tonegawa, B T Hyman.   

Abstract

The normal functional neurobiology of the Alzheimer's disease (AD) related gene presenilin 1 (PS1) is unknown. One clue comes from a genetic screen of Caenorhabditis elegans, which reveals that the presenilin homologue sel-12 facilitates lin-12 function [D. Levitan, I. Greenwald, Facilitation of lin-12-mediated signalling by sel-12, a Caenorhabditis elegans S182 Alzheimer's disease gene, Nature 377 (1995) 351-355]. The mammalian homologue of lin-12, Notch1, is a transmembrane receptor that plays an important role in cell fate decisions during development, including neurogenesis, but does not have a known function in fully differentiated cells. To better understand the potential role of Notch1 in mammalian postmitotic neurons and to test the hypothesis that Notch and PS 1 interact, we studied the effect of Notch1 transfection on neurite outgrowth in primary cultures of hippocampal/cortical neurons. We demonstrate that Notch1 inhibits neurite extension, and thus has a function in postmitotic mature neurons in the mammalian CNS. Furthermore, we present evidence demonstrating that there is a functional interaction between PS1 and Notch1 in mammalian neurons, analogous to the sel-12/lin-12 interaction in vulval development in C. elegans [D. Levitan, T. Doyle, D. Brousseau, M. Lee, G. Thinakaran, H. Slunt, S. Sisodia, I. Greenwald, Assessment of normal and mutant human presenilin function in Caenorhabditis elegans, Proc. Natl. Acad. Sci. U.S.A. 93 (1996) 14940-14944; D. Levitan, I. Greenwald, Effect of Sel-12 presenilin on Lin-12 localization and function in Caenorhabditis elegans, Development, 125 (1998) 3599-3606]. The inhibitory effect of Notch1 on neurite outgrowth is markedly attenuated in neurons from PS1 knockout mice, and enhanced in neurons from transgenic mice overexpressing wild type PS1, but not mutant PS1. These data suggest that PS1 facilitates Notch1 function in mammalian neurons, and support the hypothesis that a functional interaction exists between PS1 and Notch1 in postmitotic mammalian neurons. Copyright 1999 Elsevier Science B.V.

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Year:  1999        PMID: 10366748     DOI: 10.1016/s0169-328x(99)00119-9

Source DB:  PubMed          Journal:  Brain Res Mol Brain Res        ISSN: 0169-328X


  15 in total

1.  Notch is required for long-term memory in Drosophila.

Authors:  Asaf Presente; Randy S Boyles; Christine N Serway; J Steven de Belle; Andrew J Andres
Journal:  Proc Natl Acad Sci U S A       Date:  2004-01-29       Impact factor: 11.205

Review 2.  An overview of notch signaling in adult tissue renewal and maintenance.

Authors:  Chihiro Sato; Guojun Zhao; Ma Xenia G Ilagan
Journal:  Curr Alzheimer Res       Date:  2012-02       Impact factor: 3.498

3.  Presenilin-1 mutations reduce cytoskeletal association, deregulate neurite growth, and potentiate neuronal dystrophy and tau phosphorylation.

Authors:  G Pigino; A Pelsman; H Mori; J Busciglio
Journal:  J Neurosci       Date:  2001-02-01       Impact factor: 6.167

4.  Familial Alzheimer's disease presenilin 1 mutations cause alterations in the conformation of presenilin and interactions with amyloid precursor protein.

Authors:  Oksana Berezovska; Alberto Lleo; Lauren D Herl; Matthew P Frosch; Edward A Stern; Brian J Bacskai; Bradley T Hyman
Journal:  J Neurosci       Date:  2005-03-16       Impact factor: 6.167

5.  Oxidative stress and lipid peroxidation are upstream of amyloid pathology.

Authors:  Muriel Arimon; Shuko Takeda; Kathryn L Post; Sarah Svirsky; Bradley T Hyman; Oksana Berezovska
Journal:  Neurobiol Dis       Date:  2015-06-21       Impact factor: 5.996

Review 6.  Presenilins and APP in neuritic and synaptic plasticity: implications for the pathogenesis of Alzheimer's disease.

Authors:  Sic L Chan; Katsutoshi Furukawa; Mark P Mattson
Journal:  Neuromolecular Med       Date:  2002       Impact factor: 3.843

7.  Presenilin-1 regulates the neuronal threshold to excitotoxicity both physiologically and pathologically.

Authors:  M Grilli; E Diodato; G Lozza; R Brusa; M Casarini; D Uberti; R Rozmahel; D Westaway; P St George-Hyslop; M Memo; E Ongini
Journal:  Proc Natl Acad Sci U S A       Date:  2000-11-07       Impact factor: 11.205

8.  Dendritic spine abnormalities in amyloid precursor protein transgenic mice demonstrated by gene transfer and intravital multiphoton microscopy.

Authors:  Tara L Spires; Melanie Meyer-Luehmann; Edward A Stern; Pamela J McLean; Jesse Skoch; Paul T Nguyen; Brian J Bacskai; Bradley T Hyman
Journal:  J Neurosci       Date:  2005-08-03       Impact factor: 6.167

9.  Presenilin-1 adopts pathogenic conformation in normal aging and in sporadic Alzheimer's disease.

Authors:  Lara Wahlster; Muriel Arimon; Navine Nasser-Ghodsi; Kathryn Leigh Post; Alberto Serrano-Pozo; Kengo Uemura; Oksana Berezovska
Journal:  Acta Neuropathol       Date:  2012-11-09       Impact factor: 17.088

10.  Hierarchical clustering of gene expression patterns in the Eomes + lineage of excitatory neurons during early neocortical development.

Authors:  David A Cameron; Frank A Middleton; Anjen Chenn; Eric C Olson
Journal:  BMC Neurosci       Date:  2012-08-01       Impact factor: 3.288

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