| Literature DB >> 15115439 |
Anja Clermont1, Marianne Wedde, Volkhard Seitz, Lars Podsiadlowski, Dido Lenze, Michael Hummel, Andreas Vilcinskas.
Abstract
The first IMPI (inhibitor of metalloproteinases from insects) was identified in the greater wax moth, Galleria mellonella [Wedde, Weise, Kopacek, Franke and Vilcinskas (1998) Eur. J. Biochem. 255, 535-543]. Here we report cloning and expression of a cDNA coding for this IMPI. The IMPI mRNA was identified among the induced transcripts from a subtractive and suppressive PCR analysis after bacterial challenge of G. mellonella larvae. Induced expression of the IMPI during a humoral immune response was confirmed by real-time PCR, which documented up to 500 times higher amounts of IMPI mRNA in immunized larvae in comparison with untreated ones. The IMPI sequence shares no similarity with those of tissue inhibitors of metalloproteinases or other natural inhibitors of metalloproteinases, and the recombinant IMPI specifically inhibits thermolysin-like metalloproteinases, but not matrix metalloproteinases. These results support the hypothesis that the IMPI represents a novel type of immune-related protein which is induced and processed during the G. mellonella humoral immune response to inactivate pathogen-associated thermolysin-like metalloproteinases.Entities:
Mesh:
Substances:
Year: 2004 PMID: 15115439 PMCID: PMC1133944 DOI: 10.1042/BJ20031923
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857