ICAMs redistributed by chemokines to cellular uropods as a mechanism for recruitment of T lymphocytes

J Cell Biol. 1997 Apr 21;137(2):493-508. doi: 10.1083/jcb.137.2.493.

Abstract

The recruitment of leukocytes from the bloodstream is a key step in the inflammatory reaction, and chemokines are among the main regulators of this process. During lymphocyte-endothelial interaction, chemokines induce the polarization of T lymphocytes, with the formation of a cytoplasmic projection (uropod) and redistribution of several adhesion molecules (ICAM-1,-3, CD43, CD44) to this structure. Although it has been reported that these cytokines regulate the adhesive state of integrins in leukocytes, their precise mechanisms of chemoattraction remain to be elucidated. We have herein studied the functional role of the lymphocyte uropod. Confocal microscopy studies clearly showed that cell uropods project away from the cell bodies of adhered lymphocytes and that polarized T cells contact other T cells through the uropod structure. Time-lapse videomicroscopy studies revealed that uropod-bearing T cells were able, through this cellular projection, to contact, capture, and transport additional bystander T cells. Quantitative analysis revealed that the induction of uropods results in a 5-10-fold increase in cell recruitment. Uropod-mediated cell recruitment seems to have physiological relevance, since it was promoted by both CD45R0+ peripheral blood memory T cells as well as by in vivo activated lymphocytes. Additional studies showed that the cell recruitment mediated by uropods was abrogated with antibodies to ICAM-1, -3, and LFA-1, whereas mAb to CD43, CD44, CD45, and L-selectin did not have a significant effect, thus indicating that the interaction of LFA-1 with ICAM-1 and -3 appears to be responsible for this process. To determine whether the increment in cell recruitment mediated by uropod may affect the transendothelial migration of T cells, we carried out chemotaxis assays through confluent monolayers of endothelial cells specialized in lymphocyte extravasation. An enhancement of T cell migration was observed under conditions of uropod formation, and this increase was prevented by incubation with either blocking anti-ICAM-3 mAbs or drugs that impair uropod formation. These data indicate that the cell interactions mediated by cell uropods represent a cooperative mechanism in lymphocyte recruitment, which may act as an amplification system in the inflammatory response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Adhesion Molecules / analysis*
  • Cell Adhesion Molecules / physiology
  • Cell Communication / immunology
  • Cell Membrane / chemistry
  • Cell Polarity
  • Cells, Cultured
  • Chemokines / pharmacology*
  • Chemotaxis, Leukocyte / immunology*
  • Cytoplasm / immunology*
  • Endothelium, Vascular / immunology
  • Humans
  • Immunologic Memory
  • Leukocyte Common Antigens / analysis
  • Lymphocyte Activation
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / immunology

Substances

  • Cell Adhesion Molecules
  • Chemokines
  • Leukocyte Common Antigens