T cell gelatinases mediate basement membrane transmigration in vitro

  • J Immunol. 1995 May 1;154(9):4379-89.
D Leppert  1 E Waubant R Galardy N W Bunnett S L Hauser
Affiliations
  • 1. Department of Neurology, University of California at San Francisco 94143, USA.
PMID: 7722295
Abstract

T cell homing into extravascular sites requires penetration across the subendothelial basal lamina, a specialized nonfibrillar connective tissue structure that anchors endothelial cells to parenchymal surfaces. Herein, we show that normal human T cells express gelatinases A and B, two Matrix Metalloproteinases active against the major basal lamina constituents, Collagen types IV and V. Expression is confirmed at both the mRNA and protein levels. Gelatinase B is expressed constitutively, whereas gelatinases A and B expression is induced by T cell activation. In vitro migration of resting T cells across a basal lamina equivalent is mediated by gelatinase B, because it is specifically blocked by GM6001, a hydroxamic acid inhibitor of Matrix Metalloproteinases. Inhibition of T cell homing by interference with gelatinase function may represent a useful approach to the treatment of T cell-mediated autoimmune diseases.

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