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J Neuropathol Exp Neurol ; 62(6): 617-26, 2003 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12834106

RESUMO

Recent in vitro studies suggest that the alpha chemokine stromal-derived factor-1alpha (SDF-1alpha) and its receptor CXCR-4 may contribute to neuronal apoptosis in HIV infection of the brain. The cellular and regional expression of this chemokine and its relationship to the AIDS dementia complex (ADC), however, have remained undetermined. Using immunohistochemistry and semiquantitative RT-PCR, we examined the expression of SDF-1alpha in the frontal cortex (FC), the adjacent deep white matter (DWM). and the basal ganglia (BG) of 17 patients with ADC and 5 normal controls, and the FC and temporal cortex of 6 patients with Alzheimer disease (AD). Additionally, SDF-1alpha expression was studied in 3 different neuronal cultures: differentiated SK-N-MC cells, primary human fetal neuronal, and mouse hippocampal cultures. SDF-1alpha staining was predominantly localized to astrocytes in all 3 groups in the gray matter of the FC and the BG, often in the vicinity of cortical and basal ganglia neurons, but was generally absent in the DWM. Further, the number of positive neurons was significantly greater in the BG of AIDS subjects with advanced brain disease compared to subjects with lesser disease (p = 0.029). All cultures showed prominent SDF-1alpha staining of neurons within the cytoplasm and in neurites, whereas preferential expression in GABA-ergic neurons was found in hippocampal cultures. This is the first study to show that SDF-1alpha is constitutively expressed in astrocytes of the deep and cortical gray matter as well as in neurons of the human brain. Its increased expression in basal ganglia neurons of patients with advanced HIV CNS disease suggests it may also contribute to pathogenesis.


Assuntos
Complexo AIDS Demência/metabolismo , Astrócitos/metabolismo , Quimiocinas CXC/metabolismo , Neurônios/metabolismo , Complexo AIDS Demência/genética , Complexo AIDS Demência/patologia , Doença de Alzheimer/metabolismo , Doença de Alzheimer/patologia , Animais , Astrócitos/patologia , Astrócitos/virologia , Gânglios da Base/metabolismo , Gânglios da Base/patologia , Gânglios da Base/virologia , Northern Blotting/métodos , Southern Blotting/métodos , Contagem de Células/métodos , Células Cultivadas/virologia , Quimiocina CXCL12 , Quimiocinas CXC/genética , Feto , Lobo Frontal/metabolismo , Lobo Frontal/patologia , Lobo Frontal/virologia , Regulação da Expressão Gênica , Produtos do Gene tat/metabolismo , HIV/patogenicidade , Proteína gp120 do Envelope de HIV/metabolismo , Compostos Heterocíclicos com 1 Anel/metabolismo , Hipocampo/metabolismo , Hipocampo/patologia , Hipocampo/virologia , Humanos , Imuno-Histoquímica/métodos , Técnicas In Vitro , Camundongos , Neuroblastoma/genética , Neuroblastoma/metabolismo , Neuroblastoma/patologia , Neurônios/patologia , Neurônios/virologia , RNA Mensageiro/biossíntese , Proteínas Recombinantes/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa/métodos , Fatores de Tempo , Fator de Necrose Tumoral alfa/metabolismo , Ácido gama-Aminobutírico/metabolismo , Produtos do Gene tat do Vírus da Imunodeficiência Humana
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