Lifelong expression of apolipoprotein D in the human brainstem: correlation with reduced age-related neurodegeneration
Keywords: 
Materias Investigacion::Ciencias de la Salud::Neurología
Neuroprotective
Tissues
Neural damage
Apo D protein
Issue Date: 
2013
Publisher: 
Public Library of Science
OpenAIRE: 
Ministerio de Educación y Ciencia, Fondo Europeo de Desarrollo Regional (SAF2007-64076/), Principado de Asturias (SV-PA-13-ECOEMP-80).
ISSN: 
1932-6203
Citation: 
Navarro A, Méndez E, Diaz C, del Valle E, Martínez-Pinilla E, Ordóñez C, et al. Lifelong expression of apolipoprotein D in the human brainstem: correlation with reduced age-related neurodegeneration. PLoS One. 2013 Oct;8(10)
Abstract
The lipocalin apolipoprotein D (Apo D) is upregulated in peripheral nerves following injury and in regions of the central nervous system, such as the cerebral cortex, hippocampus, and cerebellum, during aging and progression of certain neurological diseases. In contrast, few studies have examined Apo D expression in the brainstem, a region necessary for survival and generally less prone to age-related degeneration. We measured Apo D expression in whole human brainstem lysates by slot-blot and at higher spatial resolution by quantitative immunohistochemistry in eleven brainstem nuclei (the 4 nuclei of the vestibular nuclear complex, inferior olive, hypoglossal nucleus, oculomotor nucleus, facial motor nucleus, nucleus of the solitary tract, dorsal motor nucleus of the vagus nerve, and Roller`s nucleus). In contrast to cortex, hippocampus, and cerebellum, apolipoprotein D was highly expressed in brainstem tissue from subjects (N = 26, 32−96 years of age) with no history of neurological disease, and expression showed little variation with age. Expression was significantly stronger in somatomotor nuclei (hypoglossal, oculomotor, facial) than visceromotor or sensory nuclei. Both neurons and glia expressed Apo D, particularly neurons with larger somata and glia in the periphery of these brainstem centers. Immunostaining was strongest in the neuronal perinuclear region and absent in the nucleus. We propose that strong brainstem expression of Apo D throughout adult life contributes to resistance against neurodegenerative disease and age-related degeneration, possibly by preventing oxidative stress and ensuing lipid peroxidation.

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