These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Vein graft intimal hyperplasia: leukocytes and cytokine gene expression.
    Author: Hoch JR, Stark VK, Hullett DA, Turnipseed WD.
    Journal: Surgery; 1994 Aug; 116(2):463-70; discussion 470-1. PubMed ID: 8048012.
    Abstract:
    BACKGROUND: Intimal hyperplasia (IH), a cause of early graft failure, may be regulated by leukocyte-elaborated cytokines. We investigated leukocyte infiltration and cytokine gene expression in vein grafts. METHODS: Epigastric vein to femoral artery grafts were performed in Lewis rats and harvested on day 4 and weeks 1, 2, 4, 8, and 12. Neointimal areas were measured by computerized planimetry. Immunoperoxidase staining identified for macrophages, CD4+, CD8+, and major histocompatibility complex class II+ cells. Graft RNA was used in reversetranscription-polymerase chain reaction with interleukin (IL)-1 alpha, IL-2R, monocyte chemoattractant protein-1, and transforming growth factor-beta primers. RESULTS: IH was measurable at 2 weeks; the perianastomotic regions displayed greater IH than the midgraft (p < 0.05). MANOVA indicated strong location (p = 0.0001) and time (p = 0.0009) effects. Immunocytochemistry showed inflammatory infiltrates from 4 days to 4 major histocompatibility complex class II+ and primarily monocyte/macrophages, with less frequent T lymphocytes (CD4+ > CD8+). IL-1 alpha messenger RNA is expressed early, disappearing after 4 weeks. Monocyte chemoattracta t protein-1 mRNA is constitutively expressed, with up-regulation at 4 days to 4 weeks. IL-2R mRNA levels fluctuate; transforming growth factor-beta is always expressed, peaking at 4 days to 4 weeks. CONCLUSIONS: Gene expression of cytokines thought to modulate IH is up-regulated early in vein grafts. This coincides with graft infiltration by activated leukocytes before and during the development of IH.
    [Abstract] [Full Text] [Related] [New Search]