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Molecular Pathology 2001;54:1-7; doi:10.1136/mp.54.1.1
Copyright © 2001 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists.
J Clin Pathol: Mol Pathol 2001; 54:1-7
© 2001 Journal of Clinical Pathology

Review

Demystified ...

Adhesion molecule deficiencies

D Inwald1, E G Davies2 and N Klein3

1 Portex Department of Anaesthesia, Intensive Care and Respiratory Medicine and Immunobiology Unit, Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK
2 Department of Clinical Immunology, Great Ormond Street Hospital for Children NHS Trust, London WC1N 3JF, UK
3 Immunobiology Unit, Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK

Correspondence to:
Dr Inwald D.Inwald{at}ich.ucl.ac.uk

The basic physiology of leucocyte emigration from the intravascular space into the tissues is now known to be dependent on a class of cell surface molecules that have come to be known as adhesion molecules. Many cell–cell interactions are dependent on adhesion and signal transduction via the various adhesion molecules, particularly the integrins. The study of the functions of these molecules has been enhanced by the development of blocking and activating monoclonal antibodies, knockout mice, and by the rare "experiments of nature" in the human population, in whom there is absence or dysfunction of one of the adhesion molecules. This review describes these leucocyte adhesion defects and discusses how they have provided important insights into the function of these molecules.

Key Words: leucocyte adhesion defect • Glanzmann's thrombasthenia • integrins


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