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Hypoxia-inducible factor-1alpha DNA induced angiogenesis in a rat cerebral ischemia model.
Matsuda, Takeshi; Abe, Tatsuya; Wu, Jian Liang; Fujiki, Minoru; Kobayashi, Hidenori.
Afiliación
  • Matsuda T; Department of Neurosurgery, Oita University School of Medicine, Idaigaoka 1-1, Oita, 879-5593, Japan.
Neurol Res ; 27(5): 503-8, 2005 Jul.
Article en En | MEDLINE | ID: mdl-15978176
ABSTRACT

BACKGROUND:

Hypoxia-inducible factor-1 (HIF-1) is a transcription factor that regulates the adaptive response to hypoxia in mammalian cells. It consists of a regulatory subunit HIF-1alpha, which accumulates under hypoxic conditions, and a constitutively expressed subunit, HIF-1beta. In this study, we investigated HIF-1alpha naked DNA-induced angiogenesis in a cerebral ischemic model in vivo.

METHODS:

We utilized a rat encephalo-myo-synangiosis (EMS) model and inoculated HIF-1alpha DNA into the brain surface or the temporal muscle. We analysed whether HIF-1alpha induced angiogenic factors and collateral circulation.

RESULTS:

A histological section treated with HIF-1alpha DNA showed an increased expression of HIF1 a and VEGF with collateral circulation, in comparison with control DNA (p < 0.01). The HIF-1alpha transcription factor is able to promote significant angiogenesis development.

CONCLUSION:

These results suggest the feasibility of a novel approach for therapeutic collateral circulation of cerebral ischemia in which neovascularization may be achieved indirectly using a transcriptional regulatory strategy.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Isquemia Encefálica / Circulación Colateral / Vacunas de ADN Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Neurol Res Año: 2005 Tipo del documento: Article País de afiliación: Japón
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Isquemia Encefálica / Circulación Colateral / Vacunas de ADN Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Neurol Res Año: 2005 Tipo del documento: Article País de afiliación: Japón
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