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. 1992 Nov;216(5):600–604. doi: 10.1097/00000658-199211000-00013

The adherence of endothelial cells to Dacron induces the expression of the intercellular adhesion molecule (ICAM-1).

M S Margiotta 1, F S Robertson 1, R S Greco 1
PMCID: PMC1242680  PMID: 1359845

Abstract

The intercellular adhesion molecule (ICAM-1) is a glycoprotein expressed by endothelial cells activated by cytokines. The lymphocyte-function-associated antigen (LFA-1) is an integrin expressed by activated white blood cells. Together, this receptor-ligand pair is responsible, in part, for the localization of neutrophils at sites of inflammation. Using an in vitro model, the authors studied the binding of antibodies against ICAM-1 by human saphenous vein endothelial cells (HSVEC) adherent to Dacron and control cultureware. After adherence to Dacron pretreated with fibronectin, 24% more HSVEC-bound antibody against ICAM-1 compared with HSVEC on controls. In contrast, 90% more HSVEC adherent to Dacron incubated with whole blood bound anti-ICAM-1 antibodies. These cells bound 17.7-fold greater amounts of antibody compared with HSVEC on controls. Pretreating Dacron with plasma resulted in no increase in antibody binding compared with control. Our studies suggest that the cellular components of blood in contact with Dacron create a microenvironment that activates HSVEC and enhances ICAM-1 expression. Induction of this adhesion molecule may play a pivotal role in the migration and localization of leukocytes at the site of the vascular prosthesis.

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Selected References

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  1. Albelda S. M., Buck C. A. Integrins and other cell adhesion molecules. FASEB J. 1990 Aug;4(11):2868–2880. [PubMed] [Google Scholar]
  2. Bevilacqua M. P., Pober J. S., Mendrick D. L., Cotran R. S., Gimbrone M. A., Jr Identification of an inducible endothelial-leukocyte adhesion molecule. Proc Natl Acad Sci U S A. 1987 Dec;84(24):9238–9242. doi: 10.1073/pnas.84.24.9238. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Callow A. D. The microcosm of the arterial wall--a plea for research. J Vasc Surg. 1987 Jan;5(1):1–18. [PubMed] [Google Scholar]
  4. Chervu A., Moore W. S. An overview of intimal hyperplasia. Surg Gynecol Obstet. 1990 Nov;171(5):433–447. [PubMed] [Google Scholar]
  5. Clowes A. W., Kirkman T. R., Reidy M. A. Mechanisms of arterial graft healing. Rapid transmural capillary ingrowth provides a source of intimal endothelium and smooth muscle in porous PTFE prostheses. Am J Pathol. 1986 May;123(2):220–230. [PMC free article] [PubMed] [Google Scholar]
  6. Dustin M. L., Springer T. A. Lymphocyte function-associated antigen-1 (LFA-1) interaction with intercellular adhesion molecule-1 (ICAM-1) is one of at least three mechanisms for lymphocyte adhesion to cultured endothelial cells. J Cell Biol. 1988 Jul;107(1):321–331. doi: 10.1083/jcb.107.1.321. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Krause T. J., Robertson F. M., Liesch J. B., Wasserman A. J., Greco R. S. Differential production of interleukin 1 on the surface of biomaterials. Arch Surg. 1990 Sep;125(9):1158–1160. doi: 10.1001/archsurg.1990.01410210084013. [DOI] [PubMed] [Google Scholar]
  8. Pankowsky D. A., Ziats N. P., Topham N. S., Ratnoff O. D., Anderson J. M. Morphologic characteristics of adsorbed human plasma proteins on vascular grafts and biomaterials. J Vasc Surg. 1990 Apr;11(4):599–606. [PubMed] [Google Scholar]
  9. Rothe G., Valet G. Phagocytosis, intracellular pH, and cell volume in the multifunctional analysis of granulocytes by flow cytometry. Cytometry. 1988 Jul;9(4):316–324. doi: 10.1002/cyto.990090408. [DOI] [PubMed] [Google Scholar]
  10. Tonnesen M. G. Neutrophil-endothelial cell interactions: mechanisms of neutrophil adherence to vascular endothelium. J Invest Dermatol. 1989 Aug;93(2 Suppl):53S–58S. doi: 10.1111/1523-1747.ep12581069. [DOI] [PubMed] [Google Scholar]
  11. Zacharias R. K., Kirkman T. R., Clowes A. W. Mechanisms of healing in synthetic grafts. J Vasc Surg. 1987 Nov;6(5):429–436. doi: 10.1067/mva.1987.avs0060429. [DOI] [PubMed] [Google Scholar]
  12. Ziats N. P., Pankowsky D. A., Tierney B. P., Ratnoff O. D., Anderson J. M. Adsorption of Hageman factor (factor XII) and other human plasma proteins to biomedical polymers. J Lab Clin Med. 1990 Nov;116(5):687–696. [PubMed] [Google Scholar]

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