Cloning and expression of an inhibitor of microbial metalloproteinases from insects contributing to innate immunity

被引:59
作者
Clermont, A
Wedde, M
Seitz, V
Podsiadlowski, L
Lenze, D
Hummel, M
Vilcinskas, A
机构
[1] Univ Potsdam, Inst Biochem & Biol, D-14471 Potsdam, Germany
[2] Free Univ Berlin, Benjamin Franklin Hosp, Inst Pathol, D-12200 Berlin, Germany
[3] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[4] Free Univ Berlin, Inst Zool, D-14195 Berlin, Germany
关键词
innate immunity; insect metalloproteinase inhibitor (IMPI); microbial proteinase; pathogen; thermolysin;
D O I
10.1042/BJ20031923
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:315 / 322
页数:8
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