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PMID: 7573475 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Location of focal silver staining at endothelial gaps in inflamed venules examined by scanning electron microscopy.

The American journal of physiology ·Vol. 269 ·No. 3 Pt 1 ·1995-09-00 ·Pages L403-18

Hirata A, Baluk P, Fujiwara T, McDonald DM

Abstract

The century-old histological technique of silver nitrate staining has proven to be extremely useful for visualizing endothelial cell borders and localizing endothelial gaps, but the significance of the staining is still not fully understood. To gain some insight into what silver nitrate stains, we developed a method that enabled us to use scanning electron microscopy with backscattered and secondary electron imaging to examine silver staining at endothelial cell borders of venules of the rat tracheal mucosa. We found that in normal venules, silver lines followed the smooth contour of cell borders. However, 1 min after endothelial permeability was increased by substance P, cell borders were irregular and displaced from the silver lines by as much as 4.3 microns, and the lines were accompanied by three types of silver deposits. Most common (46% of total) were annulus-shaped silver deposits that surrounded endothelial gaps. These deposits averaged 1.5 microns in width, were positioned symmetrically across cell borders, and were located at a depth of 0.3 micron beneath the luminal surface. Many endothelial gaps were partitioned into multiple pores (mean, 2.4) by fingerlike processes of endothelial cells. Surprisingly, the gaps occupied only 5.4% of the total area of the silver deposits and constituted 0.15% of the luminal surface of the leaky postcapillary venules. A second type of silver deposit (19% of total) was positioned asymmetrically with respect to the cell border and marked sites where endothelial cell margins still overlapped but appeared to be vertically separated by obliquely oriented gaps. A third type marked gaps at three-cell junctions; these were no more abundant than deposits elsewhere around the cell perimeter, suggesting that three-cell junctions were not unusually leaky sites. We conclude that silver nitrate marks endothelial cell borders and outlines endothelial cell gaps by staining an element of intercellular junctions. The annular shape of many silver deposits around gaps suggests that junctional elements in the apposing cells are separated during gap formation but are still present at the gap perimeter.

MeSH Terms
Animals Endothelium, Vascular/pathology Intercellular Junctions/ultrastructure Male Microscopy, Electron Microscopy, Electron, Scanning Rats Rats, Inbred F344 Silver Staining and Labeling Vasculitis/pathology Venules/pathology
Chemicals
Silver
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hirata A
Cardiovascular Research Institute, University of California, San Francisco 94143, USA.
Baluk P
Fujiwara T
McDonald D M
Article Info
Journal
The American journal of physiology
Abbr.
Am J Physiol
ISSN
0002-9513
Published
1995-09-00
Pages
L403-18
Language
English
Region
United States
NLM ID
0370511
Subset
IM
Grants
NHLBI NIH HHS · HL-24136 · United States
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