REGULAR ARTICLESS

Cell Research (1999), 9, 291-303

Leukolysin/MMP25/MT6-MMP: a novel matrix metalloproteinase specifically expressed in the leukocyte lineage

PEI Duanqing

Department of Pharmacology, 6-120 Jackson Hall, 321 Church St. S.E., University of Minnesota, Minneapolis, MN 55455, USA
Tel: 612-626-1468; Fax: 612-625-8408;
E-mail: peixx003@tc.umn.edu

ABSTRACT

A novel matrix metalloproteinase (MMP) was identified from leukocytes and found to be specifically expressed by peripheral blood leukocytes among 29 different tissues examined. Named leukolysin, it encodes for 562 residues with a conserved MMP structure, i.e, pre-, pro-, catalytic-, hinge- and hemopexin-like domains, but also a RXK/RR motif, known for its role in MMP zymogen activation, and a C-terminal hydrophobic segment. Overall, leukolysin displays the strongest homology to the newly identified MT-MMP subgroup with 45% and 39% identities to MT4- and MT1-MMPs vs 30% and 31.5% to MMP1 and 3 respectively. Unlike MT4-MMP whose proteolytic activity remains undefined, a C-terminally truncated leukolysin is expressed as a strong gelatinolytic species at 28 kDa which is derived from a cell-associated 34 kDa proenzyme, presumably by furin or proprotein convertase mediated removal of the propeptide ( ~ 6 kDa). By green fluorescent protein (GFP) tagging, the intracellular proenzyme is localized to granules throughout the cell, suggesting that activation occur immediately prior to secretion. Taken together, leukolysin may be part of the proteolytic arsenal deployed by leukocytes during inflammatory responses.

Key words: MT6-MMP, MMP25, leukolysin, MMP, Matrix Remodeling, Leukocytes.

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