Constitutive expression of ICAM-1 in rat microvascular systems analyzed by laser confocal microscopy

Yutaka Iigo, Makoto Suematsu, Tomoe Higashida, Jun Ichi Oheda, Keiko Matsumoto, Yoshiyuki Wakabayashi, Yuzuru Ishimura, Masayuki Miyasaka, Tohru Takashi

Research output: Contribution to journalArticlepeer-review

Abstract

The present study aimed to demonstrate consti-tutive expression of the intercellular adhesion molecule (ICAM)-l among arterioles, capillaries, and venules in the mesentery and liver and to examine the interaction between cultured endothelial cells and leukocytes in rats. ICAM-1 expression in the microvessels in vivo was visually demonstrated by laser confocal fluorescence microscopy. A monoclonal antibody against rat ICAM-1 (1A29) was labeled with fluorescein isothiocyanate, and the binding ratio between the fluorescence and immunoglobulin was determined for data calibration. Intravascularly administered fluorescein isothiocyanate-labeled 1A29 was distributed heterogeneously among the hierarchy of microvessels in the mesentery: postcapillary venules were the major portion expressing ICAM-1 constitutively, and the density of 1A29 bound to their endothelium was at least 10 times higher than that in true capillaries and arterioles in the same mesentery. On the other hand, the liver expressed ICAM-1 abundantly in sinusoids to the extent similar to that in central venules. These results suggest that postcapillary venules serve as an active gateway with the readiness to help adhere circulating leukocytes exposed to proinfiammatory stimuli in acute inflammation.

Original languageEnglish
JournalAmerican Journal of Physiology - Heart and Circulatory Physiology
Volume42
Issue number1
Publication statusPublished - 1997

Keywords

  • Intercellular adhesion molecule-1
  • Liver
  • Microcirculation
  • Neutrophil adhesion
  • Postcapillary venule

ASJC Scopus subject areas

  • Physiology

Fingerprint Dive into the research topics of 'Constitutive expression of ICAM-1 in rat microvascular systems analyzed by laser confocal microscopy'. Together they form a unique fingerprint.

Cite this