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J Neuroinflammation ; 4: 28, 2007 Nov 26.
Artigo em Inglês | MEDLINE | ID: mdl-18039385

RESUMO

BACKGROUND: Oligodendrocyte progenitor cells (OPCs) and mature oligodendrocytes are both lost in central nervous system injury and disease. Activated microglia may play a role in OPC and oligodendrocyte loss or replacement, but it is not clear how the responses of OPCs and oligodendrocytes to activated microglia differ. METHODS: OPCs and microglia were isolated from rat cortex. OPCs were induced to differentiate into oligodendrocytes with thyroid hormone in defined medium. For selected experiments, microglia were added to OPC or oligodendrocyte cultures. Lipopolysaccharide was used to activate microglia and microglial activation was confirmed by TNFalpha ELISA. Cell survival was assessed with immunocytochemistry and cell counts. OPC proliferation and oligodendrocyte apoptosis were also assessed. RESULTS: OPCs and oligodendrocytes displayed phenotypes representative of immature and mature oligodendrocytes, respectively. Activated microglia reduced OPC survival, but increased survival and reduced apoptosis of mature oligodendrocytes. Activated microglia also underwent cell death themselves. CONCLUSION: Activated microglia may have divergent effects on OPCs and mature oligodendrocytes, reducing OPC survival and increasing mature oligodendrocyte survival. This may be of importance because activated microglia are present in several disease states where both OPCs and mature oligodendrocytes are also reacting to injury. Activated microglia may simultaneously have deleterious and helpful effects on different cells after central nervous system injury.


Assuntos
Diferenciação Celular/fisiologia , Microglia/fisiologia , Oligodendroglia/fisiologia , Células-Tronco/fisiologia , Análise de Variância , Animais , Animais Recém-Nascidos , Caspase 1/metabolismo , Comunicação Celular , Morte Celular/fisiologia , Diferenciação Celular/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Células Cultivadas , Córtex Cerebral/citologia , Ensaio de Imunoadsorção Enzimática/métodos , Fatores de Crescimento de Fibroblastos/farmacologia , Regulação da Expressão Gênica/efeitos dos fármacos , Regulação da Expressão Gênica/fisiologia , Lipopolissacarídeos/farmacologia , Fator de Crescimento Derivado de Plaquetas/farmacologia , Ratos , Ratos Long-Evans , Células-Tronco/efeitos dos fármacos , Hormônios Tireóideos/farmacologia , Fator de Necrose Tumoral alfa/metabolismo
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