Human proteinase 3 resistance to inhibition extends to alpha-2 macroglobulin - Archive ouverte HAL Access content directly
Journal Articles FEBS Journal Year : 2020

Human proteinase 3 resistance to inhibition extends to alpha-2 macroglobulin

Guillaume Gabant
Maria Juliano
  • Function : Author
Marc Moniatte
  • Function : Author
  • PersonId : 921898
Magdalena Wysocka
  • Function : Author
Adam Lesner
Martine Cadene

Abstract

Polymorphonuclear neutrophils contain at least four serine endopeptidases, namely neutrophil elastase (NE), proteinase 3 (PR3), cathepsin G (CatG), and NSP4, which contribute to the regulation of infection and of inflammatory processes. In physiological conditions, endogenous inhibitors including a2-macroglobulin (a2-M), serpins [a1-proteinase inhibitor (a1-PI)], monocyte neutrophil elastase inhibitor (MNEI), a1-antichymotrypsin, and locally produced chelonianins (elafin, SLPI) control excessive proteolytic activity of neutrophilic serine proteinases. In contrast to human NE (hNE), hPR3 is weakly inhibited by a1-PI and MNEI but not by SLPI. a2-M is a large spectrum inhibitor that traps a variety of proteinases in response to cleavage(s) in its bait region. We report here that a2-M was more rapidly processed by hNE than hPR3 or hCatG. This was confirmed by the observation that the association between a2-M and hPR3 is governed by a kass in the ≤ 10^5 M-1s-1 range. Since a2M-trapped proteinases retain peptidase activity, we first predicted the putative cleavage sites within the a2-M bait region (residues 690–728) using kinetic and molecular modeling approaches. We then identified by mass spectrum analysis the cleavage sites of hPR3 in a synthetic peptide spanning the 39-residue bait region of a2-M (39pep-a2-M). Since the 39pep-a2-M peptide and the corresponding bait area in the whole protein do not contain sequences with a high probability of specific cleavage by hPR3 and were indeed only slowly cleaved by hPR3, it can be concluded that a2-M is a poor inhibitor of hPR3. The resistance of hPR3 to inhibition by endogenous inhibitors explains at least in part its role in tissue injury during chronic inflammatory diseases and its well-recognized function of major target autoantigen in granulomatosis with polyangiitis.
Fichier principal
Vignette du fichier
2020_n_guessan_cadene_febs_j_version_auteur.pdf (2.35 Mo) Télécharger le fichier
Origin : Files produced by the author(s)
Loading...

Dates and versions

hal-02901768 , version 1 (17-07-2020)

Identifiers

Cite

Koffi N'Guessan, Renata Grzywa, Seda Seren, Guillaume Gabant, Maria Juliano, et al.. Human proteinase 3 resistance to inhibition extends to alpha-2 macroglobulin. FEBS Journal, 2020, ⟨10.1111/febs.15229⟩. ⟨hal-02901768⟩
127 View
190 Download

Altmetric

Share

Gmail Facebook X LinkedIn More