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The Circulating Protease Persephone Is an Immune Sensor for Microbial Proteolytic Activities Upstream of the Drosophila Toll Pathway.
- Source :
-
Molecular cell [Mol Cell] 2018 Feb 15; Vol. 69 (4), pp. 539-550.e6. - Publication Year :
- 2018
-
Abstract
- Microbial or endogenous molecular patterns as well as pathogen functional features can activate innate immune systems. Whereas detection of infection by pattern recognition receptors has been investigated in details, sensing of virulence factors activities remains less characterized. In Drosophila, genetic evidences indicate that the serine protease Persephone belongs to a danger pathway activated by abnormal proteolytic activities to induce Toll signaling. However, neither the activation mechanism of this pathway nor its specificity has been determined. Here, we identify a unique region in the pro-domain of Persephone that functions as bait for exogenous proteases independently of their origin, type, or specificity. Cleavage in this bait region constitutes the first step of a sequential activation and licenses the subsequent maturation of Persephone to the endogenous cysteine cathepsin 26-29-p. Our results establish Persephone itself as an immune receptor able to sense a broad range of microbes through virulence factor activities rather than molecular patterns.<br /> (Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Drosophila Proteins metabolism
Drosophila melanogaster enzymology
Drosophila melanogaster growth & development
Female
Male
Proteolysis
Serine Endopeptidases metabolism
Serine Proteases metabolism
Signal Transduction
Toll-Like Receptors metabolism
Beauveria enzymology
Drosophila Proteins immunology
Drosophila melanogaster immunology
Immunity, Innate immunology
Receptors, Immunologic metabolism
Serine Endopeptidases immunology
Serine Proteases immunology
Toll-Like Receptors immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4164
- Volume :
- 69
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Molecular cell
- Publication Type :
- Academic Journal
- Accession number :
- 29452635
- Full Text :
- https://doi.org/10.1016/j.molcel.2018.01.029