Cell and Tissue Research

, Volume 284, Issue 3, pp 415–423

Expression of adhesion molecules is specific and time-dependent in cytokine-stimulated endothelial cells in culture

Authors

  • Dimitri Scholz
    • Max-Planck-Institute, Department of Experimental Cardiology, Benekestrasse 2, D-61231 Bad Nauheim, Germany
  • Bruno Devaux
    • Max-Planck-Institute, Department of Experimental Cardiology, Benekestrasse 2, D-61231 Bad Nauheim, Germany
  • Annette Hirche
    • Max-Planck-Institute, Department of Experimental Cardiology, Benekestrasse 2, D-61231 Bad Nauheim, Germany
  • Bernd Pötzsch
    • Kerckhoff Clinic, Bad Nauheim, Germany
  • Bettina Kropp
    • Kerckhoff Clinic, Bad Nauheim, Germany
  • Wolfgang Schaper
    • Max-Planck-Institute, Department of Experimental Cardiology, Benekestrasse 2, D-61231 Bad Nauheim, Germany
  • Jutta Schaper
    • Max-Planck-Institute, Department of Experimental Cardiology, Benekestrasse 2, D-61231 Bad Nauheim, Germany

DOI: 10.1007/s004410050602

Cite this article as:
Scholz, D., Devaux, B., Hirche, A. et al. Cell Tissue Res (1996) 284: 415. doi:10.1007/s004410050602

Abstract.

The time course of expression of the adhesion molecules E-selectin, VCAM-1, ICAM-1 and PECAM-1 was studied in interleukin-1β-stimulated human umbilical vein cells (HUVEC) and the subcellular sites of synthesis were determined by means of fluorescence immunohistochemistry. The maximal number of cells labelled for E-selectin was observed at 2–4 h, for VCAM-1 at 4–8 h and ICAM-1 at 6–72 h. At 8 h, E-selectin and VCAM-1 started to disappear, but ICAM-1-positive cells persisted. PECAM-1 was constitutively expressed. De novo synthesis for E-selectin started at 1 h and for both, VCAM-1 and ICAM-1 at 1.5–2 h. Maximal synthetic activity was observed at 2.5–4 h for E-selectin and at 4–6 h for VCAM-1 and ICAM-1; thereafter, synthesis slowly decreased. Transport granules occurred at 1.5 h for E-selectin and 4 h for VCAM-1; they were absent for ICAM-1. Diffuse cellular and membrane labelling indicative of the functional activity of the adhesion molecules began at 2–4 h for E-selectin, and 4 h for VCAM, but was constitutively present for ICAM-1. In conclusion, each adhesion molecule shows a specific time-dependent course of appearance and disappearance in interleukin-1β-stimulated HUVECs in accordance with their physiological role in vivo. These morphological results confirm data obtained by flow cytometry and Western blotting, but they provide new information about the behaviour of individual cells with regard to the sites of synthesis and cellular localization of the adhesion molecules.

Key words: Adhesion moleculesHuman umbilical vein endothelial cellsCytokinesCell cultureImmunohistochemistry

Copyright information

© Springer-Verlag Berlin Heidelberg 1996