scholarly journals The effect of cannabinoids on APP, BACE1, and ApoE mRNA expression

SURG Journal ◽  
2014 ◽  
Vol 7 (1) ◽  
pp. 47-55
Author(s):  
Navjit Brar

Alzheimer's disease (AD) is an age-related neurodegenerative condition associated with cognitive decline. The pathological hallmark of this disease is the deposition of β-amyloid protein plaques (Aβ) in the brain, which evoke neuronal cell death and impair inter-neuronal communication. Past studies have suggested that cannabinoids reduce the levels of Aβ in the brain; however, little is known about the mechanisms involved in this process. In this study, the SH-SY5Y cell line was first examined for expression of amyloid precursor protein (APP), beta-site APP cleaving enzyme 1 (BACE1), and apolipoprotein E (ApoE), genes involved in Aβ production and clearance. All three genes were expressed and detected in the cell line. We then observed the effects of the endocannabinoid anandamide, a CB1 receptor agonist, on the mRNA expression of APP, BACE1, and ApoE in SH-SY5Y cells. After 48h exposure to anandamide, mRNA levels of APP and BACE1 significantly decreased, which could contribute to reduced Aβ levels. The mechanism of action by which anandamide reduces mRNA levels of APP and BACE1 should be further investigated. ApoE mRNA levels were not found to be significantly changed, suggesting that anandamide does not affect mRNA expression of this gene. The effects of cannabinoids on ApoE levels should be further studied as the effects may occur at a level different from mRNA expression and may even occur via a pathway unrelated to CB1 receptor activation. Keywords: Alzheimer’s disease; β-amyloid; anandamide; amyloid precursor protein; beta-site APP cleaving enzyme 1; apolipoprotein E

2005 ◽  
Vol 65 (1) ◽  
pp. 69-75 ◽  
Author(s):  
Maria Luiza Nunes Mamede Rosa ◽  
Francisco Silveira Guimarães ◽  
Rubia Maria Welfort de Oliveira ◽  
Cláudia Maria Padovan ◽  
Ronald Carl Alan Pearson ◽  
...  

1995 ◽  
Vol 2 (3) ◽  
pp. 177-187 ◽  
Author(s):  
Anja Leona Biere ◽  
Beth Ostaszewski ◽  
Hongwei Zhao ◽  
Susan Gillespie ◽  
Steven G. Younkin ◽  
...  

Biomedicines ◽  
2020 ◽  
Vol 8 (8) ◽  
pp. 272
Author(s):  
Anaïs Bécot ◽  
Charlotte Volgers ◽  
Guillaume van Niel

In Alzheimer′s disease (AD), endolysosomal dysfunctions are amongst the earliest cellular features to appear. Each organelle of the endolysosomal system, from the multivesicular body (MVB) to the lysosome, contributes to the homeostasis of amyloid precursor protein (APP) cleavage products including β-amyloid (Aβ) peptides. Hence, this review will attempt to disentangle how changes in the endolysosomal system cumulate to the generation of toxic amyloid species and hamper their degradation. We highlight that the formation of MVBs and the generation of amyloid species are closely linked and describe how the molecular machineries acting at MVBs determine the generation and sorting of APP cleavage products towards their degradation or release in association with exosomes. In particular, we will focus on AD-related distortions of the endolysomal system that divert it from its degradative function to favour the release of exosomes and associated amyloid species. We propose here that such an imbalance transposed at the brain scale poses a novel concept of transmissible endosomal intoxication (TEI). This TEI would initiate a self-perpetuating transmission of endosomal dysfunction between cells that would support the propagation of amyloid species in neurodegenerative diseases.


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