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J Neuropathol Exp Neurol ; 62(6): 617-26, 2003 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-12834106

RESUMEN

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.


Asunto(s)
Complejo SIDA Demencia/metabolismo , Astrocitos/metabolismo , Quimiocinas CXC/metabolismo , Neuronas/metabolismo , Complejo SIDA Demencia/genética , Complejo SIDA Demencia/patología , Enfermedad de Alzheimer/metabolismo , Enfermedad de Alzheimer/patología , Animales , Astrocitos/patología , Astrocitos/virología , Ganglios Basales/metabolismo , Ganglios Basales/patología , Ganglios Basales/virología , Northern Blotting/métodos , Southern Blotting/métodos , Recuento de Células/métodos , Células Cultivadas/virología , Quimiocina CXCL12 , Quimiocinas CXC/genética , Feto , Lóbulo Frontal/metabolismo , Lóbulo Frontal/patología , Lóbulo Frontal/virología , Regulación de la Expresión Génica , Productos del Gen tat/metabolismo , VIH/patogenicidad , Proteína gp120 de Envoltorio del VIH/metabolismo , Compuestos Heterocíclicos con 1 Anillo/metabolismo , Hipocampo/metabolismo , Hipocampo/patología , Hipocampo/virología , Humanos , Inmunohistoquímica/métodos , Técnicas In Vitro , Ratones , Neuroblastoma/genética , Neuroblastoma/metabolismo , Neuroblastoma/patología , Neuronas/patología , Neuronas/virología , ARN Mensajero/biosíntesis , Proteínas Recombinantes/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa/métodos , Factores de Tiempo , Factor de Necrosis Tumoral alfa/metabolismo , Ácido gamma-Aminobutírico/metabolismo , Productos del Gen tat del Virus de la Inmunodeficiencia Humana
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