TY - JOUR
T1 - Increased expression of RXRα in dementia
T2 - An early harbinger for the cholesterol dyshomeostasis?
AU - Akram, Afia
AU - Schmeidler, James
AU - Katsel, Pavel
AU - Hof, Patrick R.
AU - Haroutunian, Vahram
N1 - Funding Information:
This research was supported by NIH grants P01 AG02219 and AG05138.
PY - 2010
Y1 - 2010
N2 - Background. Cholesterol content of cerebral membranes is tightly regulated by elaborate mechanisms that balance the level of cholesterol synthesis, uptake and efflux. Among the conventional regulatory elements, a recent research focus has been nuclear receptors, a superfamily of ligand-activated transcription factors providing an indispensable regulatory framework in controlling cholesterol metabolism pathway genes. The mechanism of transcriptional regulation by nuclear receptors such as LXRs involves formation of heterodimers with RXRs. LXR/RXR functions as a sensor of cellular cholesterol concentration and mediates cholesterol efflux by inducing the transcription of key cholesterol shuffling vehicles namely, ATP-binding cassette transporter A1 (ABCA1) and ApoE. Results. In the absence of quantitative data from humans, the relevance of expression of nuclear receptors and their involvement in cerebral cholesterol homeostasis has remained elusive. In this work, new evidence is provided from direct analysis of human postmortem brain gene and protein expression suggesting that RXR, a key regulator of cholesterol metabolism is differentially expressed in individuals with dementia. Importantly, RXR expression showed strong association with ABCA1 and ApoE gene expression, particularly in AD vulnerable regions. Conclusions. These findings suggest that LXR/RXR-induced upregulation of ABCA1 and ApoE levels may be the molecular determinants of cholesterol dyshomeostasis and of the accompanying dementia observed in AD.
AB - Background. Cholesterol content of cerebral membranes is tightly regulated by elaborate mechanisms that balance the level of cholesterol synthesis, uptake and efflux. Among the conventional regulatory elements, a recent research focus has been nuclear receptors, a superfamily of ligand-activated transcription factors providing an indispensable regulatory framework in controlling cholesterol metabolism pathway genes. The mechanism of transcriptional regulation by nuclear receptors such as LXRs involves formation of heterodimers with RXRs. LXR/RXR functions as a sensor of cellular cholesterol concentration and mediates cholesterol efflux by inducing the transcription of key cholesterol shuffling vehicles namely, ATP-binding cassette transporter A1 (ABCA1) and ApoE. Results. In the absence of quantitative data from humans, the relevance of expression of nuclear receptors and their involvement in cerebral cholesterol homeostasis has remained elusive. In this work, new evidence is provided from direct analysis of human postmortem brain gene and protein expression suggesting that RXR, a key regulator of cholesterol metabolism is differentially expressed in individuals with dementia. Importantly, RXR expression showed strong association with ABCA1 and ApoE gene expression, particularly in AD vulnerable regions. Conclusions. These findings suggest that LXR/RXR-induced upregulation of ABCA1 and ApoE levels may be the molecular determinants of cholesterol dyshomeostasis and of the accompanying dementia observed in AD.
UR - https://www.scopus.com/pages/publications/77956526504
U2 - 10.1186/1750-1326-5-36
DO - 10.1186/1750-1326-5-36
M3 - Article
AN - SCOPUS:77956526504
SN - 1750-1326
VL - 5
JO - Molecular Neurodegeneration
JF - Molecular Neurodegeneration
IS - 1
M1 - 36
ER -