Hostname: page-component-7bb8b95d7b-w7rtg Total loading time: 0 Render date: 2024-09-17T12:50:12.122Z Has data issue: false hasContentIssue false
  • English
  • Français

Electron Microscopic Immunolocalization of Basic Fibroblast Growth Factor-Like Molecules in Capillary Endothelial Cells

Published online by Cambridge University Press:  02 July 2020

Ranan Gullhan Aktas  and
Robert J. Kayton
Ranan Gullhan Aktas
Affiliation:
Trakya University, Faculty of Medicine, Histology and Embryology Department, Edirne/, Turkey
Robert J. Kayton
Affiliation:
Oregon Health Sciences University, C.R.O.E.T. L606, Portland, OR97201.
Get access

Extract

Basic fibroblast growth factor (bFGF) is a potent angiogenic polypeptide. It promotes angiogenesis in vivo and in vitro by stimulating migration, proliferation and proteolytic activity of endothelial cells. Whereas several effects of exogenous bFGF on endothelial cells have been described, it has remained unclear how endogenous bFGF produced by vascular endothelial cells regulate angiogenesis.

To further investigate functional implications of the distribution of bFGF, we undertook the present study. Our aims were (i) to identify the specific location of bFGF in endothelial cells using electron microscopy immunogold labeling technique (ii) to determine the distribution of bFGF in capillaries of different types of tissues.

Tissue samples from sciatic nerve, hippocampus, adrenal gland and kidney of normal adult rats were fixed in 4% paraformaldehyde/1 to 5% glutaraldehyde and embedded in Spurr's resin. Ultrathin sections were labeled with either polyclonal (F3393-Sigma) or monoclonal antibodies (F6162-Sigma, C3316-ZymoGenetics) specific for bFGF using a two-step immunogold labeling method.

Type
Cytochemistry (Light and Electron Histochemistry)
Information
Microscopy and Microanalysis , Volume 4 , Issue S2: Proceedings: Microscopy & Microanalysis '98, Microscopy Society of America 56th Annual Meeting, Microbeam Analysis Society 32nd Annual Meeting, Atlanta, Georgia July 12-16, 1998 , July 1998 , pp. 1100 - 1101
Copyright
Copyright © Microscopy Society of America

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

References:

1-Schweigerer, L. et al., Nature 325(1987)257.CrossRefGoogle Scholar
2-Biro, S. et al., Circ. Research 74(1994)405.CrossRefGoogle Scholar
3-Eguchi, K. et al., J. Rheumatol. 19(1992)1925.Google Scholar
4-Muthukrishnan, L. et al., J. Cell Physiol. 148(1991)1.CrossRefGoogle Scholar
5-Villaschi, S. et al., Am. J. Pathol. 143(1993)181.Google Scholar
6-Casscells, W. et al., J. Clin. Invest. 85(1990)433.CrossRefGoogle Scholar
7-Yu, Z. et al., Exp. Cell Res. 204(1993)247.CrossRefGoogle Scholar
8-Cordon-Cordo, C. et al., Lab. Invest. 63(1990)832.Google Scholar
9-Vladovsky, I. et al., Proc. Natl. Acad. Sci. 84(1987)2292.CrossRefGoogle Scholar
10-McNeil, P.L. et al., J. Cell Biol. 109(1989)811.CrossRefGoogle Scholar