The response of cells localized in the brain subventricular zone (SVZ) to growth factor stimulation has been largely described for development and adult life, whereas no information on their behavior during aging is available. To address the question of whether the cells in the SVZ of old mice respond to the intracerebroventricular administration of epidermal growth factor (EGF) and nerve growth factor (NGF), we studied the distribution of proliferating cells and the effects on ChAT and brain-derived neurotrophic factor (BDNF) synthesis in forebrain and SVZ. It was found that the conjoint administration of EGF + NGF produced a major increase in ChAT expression in both forebrain and SVZ. The ChAT mRNA levels and the number of ChAT positive cells localized in the ventricular border and in the parenchyma of SVZ area were also increased significantly in the mice receiving EGF + NGF. Enhanced numbers of SVZ cells expressing proliferative markers were also discovered in EGF + NGF treated mice and some of these cells expressed cholinergic markers, as demonstrated by double immunostaining. In addition, EGF and NGF treatments significantly upregulate BDNF protein and mRNA levels in this brain region. The present study demonstrates that cells localized in SVZ of aged mouse brain retain the capacity to respond to EGF and NGF and that after stimulation with these two growth factors, the synthesis of ChAT and BDNF also increases. The implication that cells of the SVZ remain a reservoir of cholinergic and BDNF-positive neurons in aged brain opens a new perspective for understanding the role of growth factors during neurodegenerative disorders associated with aging.

EGF and NGF injected into the brain of old mice enhance BDNF and ChAT in proliferating subventricular zone

Tirassa P;Amendola T;Fiore M;Aloe L
2003

Abstract

The response of cells localized in the brain subventricular zone (SVZ) to growth factor stimulation has been largely described for development and adult life, whereas no information on their behavior during aging is available. To address the question of whether the cells in the SVZ of old mice respond to the intracerebroventricular administration of epidermal growth factor (EGF) and nerve growth factor (NGF), we studied the distribution of proliferating cells and the effects on ChAT and brain-derived neurotrophic factor (BDNF) synthesis in forebrain and SVZ. It was found that the conjoint administration of EGF + NGF produced a major increase in ChAT expression in both forebrain and SVZ. The ChAT mRNA levels and the number of ChAT positive cells localized in the ventricular border and in the parenchyma of SVZ area were also increased significantly in the mice receiving EGF + NGF. Enhanced numbers of SVZ cells expressing proliferative markers were also discovered in EGF + NGF treated mice and some of these cells expressed cholinergic markers, as demonstrated by double immunostaining. In addition, EGF and NGF treatments significantly upregulate BDNF protein and mRNA levels in this brain region. The present study demonstrates that cells localized in SVZ of aged mouse brain retain the capacity to respond to EGF and NGF and that after stimulation with these two growth factors, the synthesis of ChAT and BDNF also increases. The implication that cells of the SVZ remain a reservoir of cholinergic and BDNF-positive neurons in aged brain opens a new perspective for understanding the role of growth factors during neurodegenerative disorders associated with aging.
2003
NEUROBIOLOGIA E MEDICINA MOLECOLARE
72
557
564
NGF
Stem cells
Aging
Learning
Neurogenesis
Questo studio ha riunito varie competenza all'interno del nostro istituto permettendo di dimostrare che sia la somministrazione esogena di fattori di crescita che la loro induzione endogena risultano in un contemporeano miglioramento delle capacità cognitive e una attivazione di processi di plasticità neuronale nel cervello di roditori anziani. Una delle principali inmplicazioni di questi risultati riguarda il ruolo delle neurotrofine negli eventi associati alla disfunzione e/o degenerazione dei circuiti nervosi durante lo sviluppo e la progressione di patologie del sistema nervoso e/o il potenziale clinico derivante dalle conoscenze sui meccanismi che regolano la produzione e/o le attività delle neurotrofine nel SNC. Ulteriori informazioni sul ruolo dell'NGF nella proliferazione e differenziamento delle cellule progenitrici nel SNC e sui meccanismi di regolazione della sintesi di NGF sono reperibili nel sito www.inemm.cnr.it/aloe IMPACT FACTOR = 3,378
5
info:eu-repo/semantics/article
262
Tirassa, P; Triaca, V; Amendola, T; Fiore, M; Aloe, L
01 Contributo su Rivista::01.01 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/166786
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