Literature DB >> 24011540

Comparison of frailty of primary neurons, embryonic, and aging mouse cortical layers.

Patrick Fugistier1, Philippe G Vallet, Geneviève Leuba, Françoise Piotton, Pascale Marin, Constantin Bouras, Armand Savioz.   

Abstract

Superficial layers I to III of the human cerebral cortex are more vulnerable toward Aβ peptides than deep layers V to VI in aging. Three models of layers were used to investigate this pattern of frailty. First, primary neurons from E14 and E17 embryonic murine cortices, corresponding respectively to future deep and superficial layers, were treated either with Aβ(1-42), okadaic acid, or kainic acid. Second, whole E14 and E17 embryonic cortices, and third, in vitro separated deep and superficial layers of young and old C57BL/6J mice, were treated identically. We observed that E14 and E17 neurons in culture were prone to death after the Aβ and particularly the kainic acid treatment. This was also the case for the superficial layers of the aged cortex, but not for the embryonic, the young cortex, and the deep layers of the aged cortex. Thus, the aged superficial layers appeared to be preferentially vulnerable against Aβ and kainic acid. This pattern of vulnerability corresponds to enhanced accumulation of senile plaques in the superficial cortical layers with aging and Alzheimer's disease.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Aging; Alzheimer's disease; Aβ amyloid; Cell death; Cell viability; Cerebral cortex; Cortical layers; Cortical vulnerability; Cux2; Kainic acid; Okadaic acid; PSD-95

Mesh:

Substances:

Year:  2013        PMID: 24011540     DOI: 10.1016/j.neurobiolaging.2013.08.005

Source DB:  PubMed          Journal:  Neurobiol Aging        ISSN: 0197-4580            Impact factor:   4.673


  4 in total

1.  Age-Related Gene Expression in the Frontal Cortex Suggests Synaptic Function Changes in Specific Inhibitory Neuron Subtypes.

Authors:  Leon French; TianZhou Ma; Hyunjung Oh; George C Tseng; Etienne Sibille
Journal:  Front Aging Neurosci       Date:  2017-05-29       Impact factor: 5.750

2.  Neuroprotection against Amyloid-β-Induced DNA Double-Strand Breaks Is Mediated by Multiple Retinoic Acid-Dependent Pathways.

Authors:  Julien Colas; Natacha Chessel; Allaeddine Ouared; Emmanuelle Gruz-Gibelli; Pascale Marin; François R Herrmann; Armand Savioz
Journal:  Neural Plast       Date:  2020-03-20       Impact factor: 3.599

3.  The Vitamin A Derivative All-Trans Retinoic Acid Repairs Amyloid-β-Induced Double-Strand Breaks in Neural Cells and in the Murine Neocortex.

Authors:  Emmanuelle Gruz-Gibelli; Natacha Chessel; Clélia Allioux; Pascale Marin; Françoise Piotton; Geneviève Leuba; François R Herrmann; Armand Savioz
Journal:  Neural Plast       Date:  2016-01-03       Impact factor: 3.599

4.  Lithium alters expression of RNAs in a type-specific manner in differentiated human neuroblastoma neuronal cultures, including specific genes involved in Alzheimer's disease.

Authors:  Bryan Maloney; Yokesh Balaraman; Yunlong Liu; Nipun Chopra; Howard J Edenberg; John Kelsoe; John I Nurnberger; Debomoy K Lahiri
Journal:  Sci Rep       Date:  2019-12-04       Impact factor: 4.379

  4 in total

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