論文

査読有り
2001年6月

Immunoelectron microscopic study of PECAM-1 expression on lymphatic endothelium of the human tongue

TISSUE & CELL
  • N Ebata
  • ,
  • Y Sawa
  • ,
  • Y Nodasaka
  • ,
  • Y Yamaoka
  • ,
  • S Yoshida
  • ,
  • Y Totsuka

33
3
開始ページ
211
終了ページ
218
記述言語
英語
掲載種別
研究論文(学術雑誌)
出版者・発行元
CHURCHILL LIVINGSTONE

The expression of platelet-endothelial cell adhesion molecule-1 (PECAM-1) on lymphatic and blood vessels of the human tongue was examined with fluorescence and transmission electron microscopy (TEM), The study used anti-desmoplakins antiserum for light microscopic identification of the lymphatic vessels, plus a pre-embedding immunogold electron microscopic technique for TEM observations. Before making TEM observations, cryostat serial sections were immunostained with anti-desmoplakins or anti-PECAM-l and then embedded. Semithin sections from each cryostat section were photographed under a light microscope and compared in order to identify the lymphatic vessels expressing PECAM-1. In fluorescence microscopy, PECAM-1 expression on lymphatic vessels was weaker than that on blood vessels, TEM observations showed that PECAM-1 expression on the blood vessels was observed only on the luminal surface of the endothelium. In lymphatic vessels, PECAM-1 expression was found both on the luminal and abluminal surfaces of the endothelium. The density of the PECAM-1 reaction products was lower in lymphatic vessels than in blood vessels. The density of PECAM-1 reaction products on the luminal surface of lymphatic vessels was higher than on the abluminal surfaces. The results suggest that blood vessels are more active than lymphatic vessels in leukocyte migration. The expression of PECAM-1 on the abluminal surface of lymphatic endothelium may allow leukocytes to adhere to the endothelium and interact in their migration from tissue into lymphatic vessels. (C) 2001 Harcourt Publishers Ltd.

リンク情報
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000169853500001&DestApp=WOS_CPL
ID情報
  • ISSN : 0040-8166
  • Web of Science ID : WOS:000169853500001

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