Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/140151
Title: Heme Oxygenase-1 and Brain Oxysterols Metabolism Are Linked to Egr-1 Expression in Aged Mice Cortex, but Not in Hippocampus
Author: Rosa, Paolo
Zerbinati, Chiara
Crestini, Alessio
Canudas Teixidó, Anna-Maria
Ragona, Giuseppe
Confaloni, Annamaria
Iuliano, Luigi
Calogero, Antonella
Keywords: Envelliment
Malalties neurodegeneratives
Envelliment cerebral
Aging
Neurodegenerative Diseases
Aging brain
Issue Date: 6-Nov-2018
Publisher: Frontiers Media
Abstract: Throughout life, stress stimuli act upon the brain leading to morphological and functional changes in advanced age, when it is likely to develop neurodegenerative disorders. There is an increasing need to unveil the molecular mechanisms underlying aging, in a world where populations are getting older. Egr-1 (early growth response 1), a transcriptional factor involved in cell survival, proliferation and differentiation - with a role also in memory, cognition and synaptic plasticity, can be implicated in the molecular mechanism of the aging process. Moreover, Heme Oxygenase-1a (HO), a 32 kDa heat-shock protein that converts heme to iron, carbon monoxide and biliverdin, is a key enzyme with neuroprotective properties. Several in vitro and in vivo studies reported that HO-1 could regulate the metabolism of oxysterols, oxidation products of cholesterol that include markers of oxidative stress. Recently, a link between Egr-1 and HO-1 has been demonstrated in mouse lung cells exposed to cigarette smoke. In view of these data, we wanted to investigate whether Egr-1 can be implicated also in the oxysterol metabolism during brain aging. Our results show that Egr-1 expression is differently expressed in the cortex and hippocampus of old mice, as well as the oxysterol profile between these two brain areas. In particular, we show that the cortex experiences in an age-dependent fashion increasing levels of the Egr-1 protein, and that these correlate with the level of HO-1 expression and oxysterol abundance. Such a situation was not observed in the hippocampus. These results are further strenghtened by our observations made with Egr-1 KO mice, confirming our hypothesis concerning the influence of Egr-1 on oxysterol production and accumulation via regulation of the expression of HO-1 in the cortex, but not the hippocampus, of old mice. It is important to notice that most of the oxysterols involved in this process are those usually stimulated by oxidative stress, which would then represent the triggering factor for this mechanism. Keywords: Egr-1, aging brain, oxysterols, HO-1, oxidative stress, cortex, hippocampus
Note: Reproducció del document publicat a: https://doi.org/10.3389/fnagi.2018.00363
It is part of: Frontiers in Aging Neuroscience, 2018, vol. 10, num. 363
URI: http://hdl.handle.net/2445/140151
Related resource: https://doi.org/10.3389/fnagi.2018.00363
ISSN: 1663-4365
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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