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Dynamic MCP-1 mRNA response of human aortic endothelial cells (HAEC) to step changes in laminar shear stress

Producción científica: Conference contribution

Resumen

Our aim is to study the hemodynamic alteration of monocyte recruitment and adhesion in model blood vessel systems, focusing on the hemodynamic effects of the recruitment factor monocyte chemotactic protein one, MCP-1, gene expression in HAEC. Preconditioning with low shear stress, LS, elevates MCP-1 gene activity and eliminates any transient peak in activity upon switching to high shear stress, HS, without affecting HS-induced gene down-regulation. These data suggest an interaction between the pathways mediating the long term response to LS and the transient cellular response to HS onset.

Idioma originalEnglish (US)
Título de la publicación alojadaAnnual International Conference of the IEEE Engineering in Medicine and Biology - Proceedings
EditorialIEEE
Páginas4
Número de páginas1
ISBN (versión impresa)0780356756
EstadoPublished - 1999
EventoProceedings of the 1999 IEEE Engineering in Medicine and Biology 21st Annual Conference and the 1999 Fall Meeting of the Biomedical Engineering Society (1st Joint BMES / EMBS) - Atlanta, GA, USA
Duración: oct 13 1999oct 16 1999

Serie de la publicación

NombreAnnual International Conference of the IEEE Engineering in Medicine and Biology - Proceedings
Volumen1
ISSN (versión impresa)0589-1019

Other

OtherProceedings of the 1999 IEEE Engineering in Medicine and Biology 21st Annual Conference and the 1999 Fall Meeting of the Biomedical Engineering Society (1st Joint BMES / EMBS)
CiudadAtlanta, GA, USA
Período10/13/9910/16/99

ASJC Scopus subject areas

  • Signal Processing
  • Biomedical Engineering
  • Computer Vision and Pattern Recognition
  • Health Informatics

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Profundice en los temas de investigación de 'Dynamic MCP-1 mRNA response of human aortic endothelial cells (HAEC) to step changes in laminar shear stress'. En conjunto forman una huella única.

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