Skip to main content
Log in

Increased blood–brain barrier permeability and endothelial abnormalities induced by vascular endothelial growth factor

  • Published:
Journal of Neurocytology

Abstract

The early effects of intracerebrally infused vascular endothelial growth factor (VEGF) on the blood–brain barrier (BBB) to endogenous albumin were studied using a quantitative immunocytochemical procedure. In addition, transmission electron microscopy was used to observe morphological changes induced in brain vasculature. A solution of VEGF in saline (40 ng/10 μl) was infused into the parieto-occipital cortex of mice, which were killed 10 min, 30 min, and 24 h afterwards. Untreated mice and mice that received infusion of saline only were used as controls. For immunocytochemical evaluation, ultrathin sections of immersion-fixed brain samples embedded in Lowicryl K4M were exposed to anti-albumin antiserum followed by protein A-gold. Simultaneously, other brain samples embedded in Spurr resin were used for ultrastructural examination. Morphometric and statistical analysis indicated that as soon as 10 min after infusion of VEGF, 33% of vascular profiles were leaking albumin, and this value increased at 30 min to 92%. This effect of VEGF appears to be of rather short duration because after 24 h, only 27% of vascular profiles showed signs of leakage. The results of ultrastructural observations indicate that VEGF (30 min post-infusion) induces several changes in microvascular segments located in the area of intracerebral infusion of VEGF. These changes consist of the appearance of interendothelial gaps; fragmentation of the endothelium with formation of segmental, fenestrae-like narrowings; degenerative changes of the vascular basement membrane; and the appearance of fibrin gel in the vessel lumen. At 24 h post-infusion, solitary diaphragmed fenestrae appeared in attenuated segments of the endothelium in a few microvascular profiles. These changes, which are interpreted to be preparatory steps for angiogenesis, affect the structural integrity of the vascular segments, leading to extravasation of blood plasma proteins, including albumin. © 1998 Chapman and Hall

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Audus, K. L. & Raub, T. J. (1993) Lysosomes of brain and other vascular endothelia. In The BloodBrain Barrier (edited by Pardridge, W. M.) pp. 201–27. New York: Raven Press.

    Google Scholar 

  • Bates, D. O. & Curry, F. E. (1996) Vascular endothelial growth factor increases hydraulic conductivity of isolated perfused microvessels. American Journal of Physiology 271, H2520–28.

    Google Scholar 

  • Breier, G., Albrecht, U., Sterrer, S. & Risau, W. (1992) Expression of vascular endothelial growth factor during embryonic angiogenesis and endothelial cell differentiation. Development 114, 521–32.

    Google Scholar 

  • Brightman, M. W. (1989) The anatomic basis of the blood–brain barrier. In Implications of the BloodBrain Barrier and its Manipulation (edited by Neuwelt, E. A.) Vol. 1, pp. 53–83. New York: Plenum Medical Book Company.

    Google Scholar 

  • Brightman, M. W. & Reese, T. S. (1969) Junctions between intimately apposed cell membranes in the vertebrate brain. Journal of Cell Biology 40, 648–77.

    Google Scholar 

  • Drake, C. J. & Little, C. D. (1995) Exogenous vascular endothelial growth factor induces malformed and hyperfused vessels during embryonic neovascularization.Proceedings of the National Academy of Sciences USA 92, 7657–61.

    Google Scholar 

  • Dvorak, H. F., Brown, L. F., Detmar, M. & Dvorak, A. M. (1995) Vascular permeability factor/vascular endothelial growth factor, microvascular hyperpermeability, and angiogenesis. American Journal of Pathology 146, 1029–39.

    Google Scholar 

  • Engelhardt, B. & Risau, W. (1995) Development of the blood–brain barrier. In New Concepts of a BloodBrain Barrier (edited by Greenwood, J., Bergley, D. J. & Segal, M. B.) pp. 11–31. New York: Plenum Press.

    Google Scholar 

  • Ghitescu, L. & Bendayan, M. (1992) Transendothelial transport of serum albumin: a quantitative immunocytochemical study. Journal of Cell Biology 117, 745–55.

    Google Scholar 

  • Kaya, M., Chang, L., Truong, A. & Brightman, M. W. (1996a) Chemical induction of fenestrae in vessels of the blood–brain barrier. Experimental Neurology 142, 6–13.

    Google Scholar 

  • Kaya, M., Chang, L., Truong, A. & Brightman, M. W. (1996b) Effects of urokinase and vascular endothelial growth factor (VEGF) on brain vessels. Society for Neuroscience Abstracts 22, 53.

    Google Scholar 

  • Keck, P. J., Hauser, S. D., Krivi, G., Sanzo, K., Warren, T., Feder, J. & Connolly, D. T. (1989) Vascular permeability factor, an endothelial cell mitogen related to PDGF. Science 246, 1309–12.

    Google Scholar 

  • Leung, D. W., Cachianes, G., Kuang, W. J., Goeddel, D. V. & Ferrara, N. (1989) Vascular endothelial growth factor is a secreted angiogenic mitogen. Science 246, 1306–9.

    Google Scholar 

  • Lin, S.-J., Jan, K-M., Schuessler, G., Weinbaum, S. & Chien, S. (1988) Enhanced macromolecular permeability of aortic endothelial cells in association with mitosis. Atherosclerosis 73, 223–32.

    Google Scholar 

  • Neal, C. R. & Michel, C. C. (1995) Transcellular gaps in microvascular walls of frog and rat when permeability is increased by perfusion with the ionophore A23187. Journal of Physiology 488, 427–37.

    Google Scholar 

  • Neal, C. R. & Michel, C. C. (1997a) Vascular endothelial growth factor (VEGF) increases permeability by inducing openings through endothelial cells. International Journal of Microcirculation 17, 204 (Abstract).

    Google Scholar 

  • Neal, C. R. & Michel, C. C. (1997b) Transcellular openings through frog microvascular endothelium. Experimental Physiology 82, 419–22.

    Google Scholar 

  • Roberts, W. G. & Palade, G. E. (1995) Increased microvascular permeability and endothelial fenestration induced by vascular endothelial growth factor. Journal of Cell Science 108, 2369–79.

    Google Scholar 

  • Robertson, P. L., Dubois, M., Bowman, P. D. & Goldstein, G. W. (1985) Angiogenesis in developing rat brain: an in vivo and in vitro study. Developmental Brain Research 23, 219–23.

    Google Scholar 

  • Schimmenti, L. A., Yan, H. C., Madri, J. A. & Albelda, S. M. (1992) Platelet endothelial cell adhesion molecule, PECAM-1, modulates cell migration. Journal of Cell Physiology 153, 417–28.

    Google Scholar 

  • Senger, D. R., Galli, S. J., Dvorak, A. M., Perruzzi, C. A., Harvey, V. S. & Dvorak, H. F. (1983) Tumor cells secrete a vascular permeability factor that promotes accumulation of ascites fluid. Science 219, 983–5.

    Google Scholar 

  • Thomas, K. A. (1996) Vascular endothelial growth factor, a potent and selective angiogenic agent. Journal of Biological Chemistry 271, 603–6.

    Google Scholar 

  • Tischer, E., Mitchell, R. & Hartman, T. (1991) The human gene for vascular endothelial growth factor. Multiple protein forms are encoded through alternative exon splicing. Journal of Biological Chemistry 266, 11947–54.

    Google Scholar 

  • Vorbrodt, A. W. (1995) The application of quantitative immunocytochemistry for the evaluation of blood–brain barrier (BBB) to endogenous albumin. In New Concepts of a BloodBrain Barrier (edited by Greenwood, J., Begley, D. J. & Segal, M. B.) pp. 39–46. New York: Plenum Press.

    Google Scholar 

  • Vorbrodt, A. W., Lossinsky, A. S., Dobrogowska, D. H. & Wisniewski, H. M. (1993) Cellular mechanisms of the blood–brain barrier (BBB) opening to albumin-gold complex. Histology and Histopathology 8, 51–61.

    Google Scholar 

  • Vorbrodt, A. W. & Dobrogowska, D. H. (1994) Immunocytochemical evaluation of blood–brain barrier to endogenous albumin in adult, newborn and aged mice. Folia Histochemica et Cytobiologica 32, 63–70.

    Google Scholar 

  • Vorbrodt, A. W., Dobrogowska, D. H., Tarnawski, M. & Lossinsky, A. S. (1994) A quantitative immunocytochemical study of the osmotic opening of the blood–brain barrier to endogenous albumin.Journal of Neurocytology 23, 792–800.

    Google Scholar 

  • Yoshida, Y., Yamada, M., Wakabayashi, K. & Ikuta, F. (1988) Endothelial fenestrae in the rat fetal cerebrum. Developmental Brain Research 44, 211–19.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Dobrogowska, D., Lossinsky, A., Tarnawski, M. et al. Increased blood–brain barrier permeability and endothelial abnormalities induced by vascular endothelial growth factor. J Neurocytol 27, 163–173 (1998). https://doi.org/10.1023/A:1006907608230

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1006907608230

Keywords

Navigation