Molecular and Functional Characterization of the Urokinase Receptor on Human Mast Cells

• Published in: The Journal of biological chemistry Vol. 272; no. 12; pp. 7824 - 7832
• Main Authors: Sillaber, C., Baghestanian, M., Hofbauer, R., Virgolini, I., Bankl, H.C., Füreder, W., Agis, H., Willheim, M., Leimer, M., Scheiner, O., Binder, B.R., Kiener, H.P., Bevec, D., Fritsch, G., Majdic, O., Kress, H.G., Gadner, H., Lechner, K., Valent, P.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 21-03-1997; American Society for Biochemistry and Molecular Biology
• Subjects: Binding Sites; Cell Line; Cell Membrane - metabolism; Chemotaxis, Leukocyte; Histamine Release; Humans; In Situ Hybridization; Mast Cells - metabolism; Radioligand Assay; Receptors, Cell Surface - genetics; Receptors, Cell Surface - metabolism; Receptors, Urokinase Plasminogen Activator; Urokinase-Type Plasminogen Activator - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.272.12.7824

The urokinase receptor system is involved in several biological processes including extracellular proteolysis, cell invasion, and chemotaxis. Mast cells are multifunctional perivascular cells that play an important role in the regulation of microenvironmental events. We report that primary human mast cells and the human mast cell line HMC-1 express the receptor for urokinase. As assessed by Northern blotting and reverse transcription polymerase chain reaction technique, purified human lung mast cells and HMC-1 cells expressed urokinase receptor mRNA in a constitutive manner. Using a toluidine blue/immunofluorescence double staining technique and monoclonal antibodies, surface expression of urokinase receptor was demonstrable in lung, skin, uterus, heart, and tonsil mast cells, whereas the low density lipoprotein receptor-related protein was not detectable. Binding of monoclonal antibody VIM5 (recognizing the urokinase binding domain of urokinase receptor) to HMC-1 could be blocked by high molecular weight but not low molecular weight urokinase. Binding analyses performed with 123I-urokinase revealed expression of 271,000 ± 55,000 high affinity urokinase binding sites per HMC-1 cell, with a calculated dissociation constant of 1.29 ± 0.3 nM. Purified urokinase induced dose-dependent migration of primary mast cells and HMC-1 in a chemotaxis assay without inducing release of histamine. The mast cell agonist stem cell factor also induced migration of HMC-1 and caused up-regulation of expression of urokinase receptor mRNA. Together, our data show that human mast cells express functional receptors for urokinase. Expression of urokinase receptors on mast cells may have implications for mast cell-dependent microvascular processes associated with fibrinolysis, migration, or local tissue repair.