Literature DB >> 24168199

The entorhinal cortex and neurotrophin signaling in Alzheimer's disease and other disorders.

Helen E Scharfman1, Moses V Chao.   

Abstract

A major problem in the field of neurodegeneration is the basis of selective vulnerability of subsets of neurons to disease. In aging, Alzheimer's disease (AD), and other disorders such as temporal lobe epilepsy, the superficial layers of the entorhinal cortex (EC) are an area of selective vulnerability. In AD, it has been suggested that the degeneration of these neurons may play a role in causing the disease because it occurs at an early stage. Therefore, it is important to define the distinctive characteristics of the EC that make this region particularly vulnerable. It has been shown that neurotrophins such as brain-derived neurotrophic factor (BDNF) are critical to the maintenance of the cortical neurons in the adult brain, and specifically the EC. Here we review the circuitry, distinctive functions, and neurotrophin-dependence of the EC that are relevant to its vulnerability. We also suggest that a protein that is critical to the actions of BDNF, the ARMS/Kidins220 scaffold protein, plays an important role in neurotrophic support of the EC.

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Year:  2013        PMID: 24168199      PMCID: PMC3836904          DOI: 10.1080/17588928.2013.826184

Source DB:  PubMed          Journal:  Cogn Neurosci        ISSN: 1758-8928            Impact factor:   3.065


  113 in total

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6.  The ARMS/Kidins220 scaffold protein modulates synaptic transmission.

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  17 in total

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Review 5.  Androgen Modulation of Hippocampal Structure and Function.

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6.  Model scenarios for cell cycle re-entry in Alzheimer's disease.

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Review 7.  Neuroinflammatory challenges compromise neuronal function in the aging brain: Postoperative cognitive delirium and Alzheimer's disease.

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8.  Entorhinal cortical defects in Tg2576 mice are present as early as 2-4 months of age.

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10.  Intracellular amyloid β oligomers impair organelle transport and induce dendritic spine loss in primary neurons.

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