In Vitro Mode of Action and Anti-thrombotic Activity of Boophilin, a Multifunctional Kunitz Protease Inhibitor from the Midgut of a Tick Vector of Babesiosis, Rhipicephalus microplus.

BACKGROUND:Hematophagous mosquitos and ticks avoid host hemostatic system through expression of enzyme inhibitors targeting proteolytic reactions of the coagulation and complement cascades. While most inhibitors characterized to date were found in the salivary glands, relatively few others have been...

Full description

Bibliographic Details
Main Authors: Teresa C Assumpção, Dongying Ma, Daniella M Mizurini, R Manjunatha Kini, José M C Ribeiro, Michail Kotsyfakis, Robson Q Monteiro, Ivo M B Francischetti
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS Neglected Tropical Diseases
Online Access:http://europepmc.org/articles/PMC4706430?pdf=render
id doaj-ba3e1106f28645379f8830423cbc6335
record_format Article
spelling doaj-ba3e1106f28645379f8830423cbc63352020-11-25T01:46:38ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352016-01-01101e000429810.1371/journal.pntd.0004298In Vitro Mode of Action and Anti-thrombotic Activity of Boophilin, a Multifunctional Kunitz Protease Inhibitor from the Midgut of a Tick Vector of Babesiosis, Rhipicephalus microplus.Teresa C AssumpçãoDongying MaDaniella M MizuriniR Manjunatha KiniJosé M C RibeiroMichail KotsyfakisRobson Q MonteiroIvo M B FrancischettiBACKGROUND:Hematophagous mosquitos and ticks avoid host hemostatic system through expression of enzyme inhibitors targeting proteolytic reactions of the coagulation and complement cascades. While most inhibitors characterized to date were found in the salivary glands, relatively few others have been identified in the midgut. Among those, Boophilin is a 2-Kunitz multifunctional inhibitor targeting thrombin, elastase, and kallikrein. However, the kinetics of Boophilin interaction with these enzymes, how it modulates platelet function, and whether it inhibits thrombosis in vivo have not been determined. METHODOLOGY/PRINCIPAL FINDINGS:Boophilin was expressed in HEK293 cells and purified to homogeneity. Using amidolytic assays and surface plasmon resonance experiments, we have demonstrated that Boophilin behaves as a classical, non-competitive inhibitor of thrombin with respect to small chromogenic substrates by a mechanism dependent on both exosite-1 and catalytic site. Inhibition is accompanied by blockade of platelet aggregation, fibrin formation, and clot-bound thrombin in vitro. Notably, we also identified Boophilin as a non-competitive inhibitor of FXIa, preventing FIX activation. In addition, Boophilin inhibits kallikrein activity and the reciprocal activation, indicating that it targets the contact pathway. Furthermore, Boophilin abrogates cathepsin G- and plasmin-induced platelet aggregation and partially affects elastase-mediated cleavage of Tissue Factor Pathway Inhibitor (TFPI). Finally, Boophilin inhibits carotid artery occlusion in vivo triggered by FeCl3, and promotes bleeding according to the mice tail transection method. CONCLUSION/SIGNIFICANCE:Through inhibition of several enzymes involved in proteolytic cascades and cell activation, Boophilin plays a major role in keeping the midgut microenvironment at low hemostatic and inflammatory tonus. This response allows ticks to successfully digest a blood meal which is critical for metabolism and egg development. Boophilin is the first tick midgut FXIa anticoagulant also found to inhibit thrombosis.http://europepmc.org/articles/PMC4706430?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Teresa C Assumpção
Dongying Ma
Daniella M Mizurini
R Manjunatha Kini
José M C Ribeiro
Michail Kotsyfakis
Robson Q Monteiro
Ivo M B Francischetti
spellingShingle Teresa C Assumpção
Dongying Ma
Daniella M Mizurini
R Manjunatha Kini
José M C Ribeiro
Michail Kotsyfakis
Robson Q Monteiro
Ivo M B Francischetti
In Vitro Mode of Action and Anti-thrombotic Activity of Boophilin, a Multifunctional Kunitz Protease Inhibitor from the Midgut of a Tick Vector of Babesiosis, Rhipicephalus microplus.
PLoS Neglected Tropical Diseases
author_facet Teresa C Assumpção
Dongying Ma
Daniella M Mizurini
R Manjunatha Kini
José M C Ribeiro
Michail Kotsyfakis
Robson Q Monteiro
Ivo M B Francischetti
author_sort Teresa C Assumpção
title In Vitro Mode of Action and Anti-thrombotic Activity of Boophilin, a Multifunctional Kunitz Protease Inhibitor from the Midgut of a Tick Vector of Babesiosis, Rhipicephalus microplus.
title_short In Vitro Mode of Action and Anti-thrombotic Activity of Boophilin, a Multifunctional Kunitz Protease Inhibitor from the Midgut of a Tick Vector of Babesiosis, Rhipicephalus microplus.
title_full In Vitro Mode of Action and Anti-thrombotic Activity of Boophilin, a Multifunctional Kunitz Protease Inhibitor from the Midgut of a Tick Vector of Babesiosis, Rhipicephalus microplus.
title_fullStr In Vitro Mode of Action and Anti-thrombotic Activity of Boophilin, a Multifunctional Kunitz Protease Inhibitor from the Midgut of a Tick Vector of Babesiosis, Rhipicephalus microplus.
title_full_unstemmed In Vitro Mode of Action and Anti-thrombotic Activity of Boophilin, a Multifunctional Kunitz Protease Inhibitor from the Midgut of a Tick Vector of Babesiosis, Rhipicephalus microplus.
title_sort in vitro mode of action and anti-thrombotic activity of boophilin, a multifunctional kunitz protease inhibitor from the midgut of a tick vector of babesiosis, rhipicephalus microplus.
publisher Public Library of Science (PLoS)
series PLoS Neglected Tropical Diseases
issn 1935-2727
1935-2735
publishDate 2016-01-01
description BACKGROUND:Hematophagous mosquitos and ticks avoid host hemostatic system through expression of enzyme inhibitors targeting proteolytic reactions of the coagulation and complement cascades. While most inhibitors characterized to date were found in the salivary glands, relatively few others have been identified in the midgut. Among those, Boophilin is a 2-Kunitz multifunctional inhibitor targeting thrombin, elastase, and kallikrein. However, the kinetics of Boophilin interaction with these enzymes, how it modulates platelet function, and whether it inhibits thrombosis in vivo have not been determined. METHODOLOGY/PRINCIPAL FINDINGS:Boophilin was expressed in HEK293 cells and purified to homogeneity. Using amidolytic assays and surface plasmon resonance experiments, we have demonstrated that Boophilin behaves as a classical, non-competitive inhibitor of thrombin with respect to small chromogenic substrates by a mechanism dependent on both exosite-1 and catalytic site. Inhibition is accompanied by blockade of platelet aggregation, fibrin formation, and clot-bound thrombin in vitro. Notably, we also identified Boophilin as a non-competitive inhibitor of FXIa, preventing FIX activation. In addition, Boophilin inhibits kallikrein activity and the reciprocal activation, indicating that it targets the contact pathway. Furthermore, Boophilin abrogates cathepsin G- and plasmin-induced platelet aggregation and partially affects elastase-mediated cleavage of Tissue Factor Pathway Inhibitor (TFPI). Finally, Boophilin inhibits carotid artery occlusion in vivo triggered by FeCl3, and promotes bleeding according to the mice tail transection method. CONCLUSION/SIGNIFICANCE:Through inhibition of several enzymes involved in proteolytic cascades and cell activation, Boophilin plays a major role in keeping the midgut microenvironment at low hemostatic and inflammatory tonus. This response allows ticks to successfully digest a blood meal which is critical for metabolism and egg development. Boophilin is the first tick midgut FXIa anticoagulant also found to inhibit thrombosis.
url http://europepmc.org/articles/PMC4706430?pdf=render
work_keys_str_mv AT teresacassumpcao invitromodeofactionandantithromboticactivityofboophilinamultifunctionalkunitzproteaseinhibitorfromthemidgutofatickvectorofbabesiosisrhipicephalusmicroplus
AT dongyingma invitromodeofactionandantithromboticactivityofboophilinamultifunctionalkunitzproteaseinhibitorfromthemidgutofatickvectorofbabesiosisrhipicephalusmicroplus
AT daniellammizurini invitromodeofactionandantithromboticactivityofboophilinamultifunctionalkunitzproteaseinhibitorfromthemidgutofatickvectorofbabesiosisrhipicephalusmicroplus
AT rmanjunathakini invitromodeofactionandantithromboticactivityofboophilinamultifunctionalkunitzproteaseinhibitorfromthemidgutofatickvectorofbabesiosisrhipicephalusmicroplus
AT josemcribeiro invitromodeofactionandantithromboticactivityofboophilinamultifunctionalkunitzproteaseinhibitorfromthemidgutofatickvectorofbabesiosisrhipicephalusmicroplus
AT michailkotsyfakis invitromodeofactionandantithromboticactivityofboophilinamultifunctionalkunitzproteaseinhibitorfromthemidgutofatickvectorofbabesiosisrhipicephalusmicroplus
AT robsonqmonteiro invitromodeofactionandantithromboticactivityofboophilinamultifunctionalkunitzproteaseinhibitorfromthemidgutofatickvectorofbabesiosisrhipicephalusmicroplus
AT ivombfrancischetti invitromodeofactionandantithromboticactivityofboophilinamultifunctionalkunitzproteaseinhibitorfromthemidgutofatickvectorofbabesiosisrhipicephalusmicroplus
_version_ 1725018232066146304