Nanoencapsulation of Gla-Rich Protein (GRP) as a novel approach to target inflammation
Main Author: | |
---|---|
Publication Date: | 2022 |
Other Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | http://hdl.handle.net/10400.1/17888 |
Summary: | Chronic inflammation is a major driver of chronic inflammatory diseases (CIDs), with a tremendous impact worldwide. Besides its function as a pathological calcification inhibitor, vitamin K-dependent protein Gla-rich protein (GRP) was shown to act as an anti-inflammatory agent independently of its gamma-carboxylation status. Although GRP’s therapeutic potential has been highlighted, its low solubility at physiological pH still constitutes a major challenge for its biomedical application. In this work, we produced fluorescein-labeled chitosan-tripolyphosphate nanoparticles containing non-carboxylated GRP (ucGRP) (FCNG) via ionotropic gelation, increasing its bioavailability, stability, and anti-inflammatory potential. The results indicate the nanosized nature of FCNG with PDI and a zeta potential suitable for biomedical applications. FCNG’s anti-inflammatory activity was studied in macrophage-differentiated THP1 cells, and in primary vascular smooth muscle cells and chondrocytes, inflamed with LPS, TNFα and IL-1β, respectively. In all these in vitro human cell systems, FCNG treatments resulted in increased intra and extracellular GRP levels, and decreased pro-inflammatory responses of target cells, by decreasing pro-inflammatory cytokines and inflammation mediators. These results suggest the retained anti-inflammatory bioactivity of ucGRP in FCNG, strengthening the potential use of ucGRP as an anti-inflammatory agent with a wide spectrum of application, and opening up perspectives for its therapeutic application in CIDs. |
id |
RCAP_f42fe18fc3e2887b58a5cb17bb45f104 |
---|---|
oai_identifier_str |
oai:sapientia.ualg.pt:10400.1/17888 |
network_acronym_str |
RCAP |
network_name_str |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
repository_id_str |
https://opendoar.ac.uk/repository/7160 |
spelling |
Nanoencapsulation of Gla-Rich Protein (GRP) as a novel approach to target inflammationNanoparticlesGla-rich protein (GRP)Chronic inflammatory diseases (CIDs)InflammationVitamin K-dependent protein (VKDP)Chronic inflammation is a major driver of chronic inflammatory diseases (CIDs), with a tremendous impact worldwide. Besides its function as a pathological calcification inhibitor, vitamin K-dependent protein Gla-rich protein (GRP) was shown to act as an anti-inflammatory agent independently of its gamma-carboxylation status. Although GRP’s therapeutic potential has been highlighted, its low solubility at physiological pH still constitutes a major challenge for its biomedical application. In this work, we produced fluorescein-labeled chitosan-tripolyphosphate nanoparticles containing non-carboxylated GRP (ucGRP) (FCNG) via ionotropic gelation, increasing its bioavailability, stability, and anti-inflammatory potential. The results indicate the nanosized nature of FCNG with PDI and a zeta potential suitable for biomedical applications. FCNG’s anti-inflammatory activity was studied in macrophage-differentiated THP1 cells, and in primary vascular smooth muscle cells and chondrocytes, inflamed with LPS, TNFα and IL-1β, respectively. In all these in vitro human cell systems, FCNG treatments resulted in increased intra and extracellular GRP levels, and decreased pro-inflammatory responses of target cells, by decreasing pro-inflammatory cytokines and inflammation mediators. These results suggest the retained anti-inflammatory bioactivity of ucGRP in FCNG, strengthening the potential use of ucGRP as an anti-inflammatory agent with a wide spectrum of application, and opening up perspectives for its therapeutic application in CIDs.MDPISapientiaViegas, CarlaAraújo, NunaCarreira, JoanaPontes, Jorge FilipeMacedo, Anjos L.Vinhas, MauríciaMoreira, Ana S.Faria, Tiago Q.Grenha, Anade Matos, António A.Schurgers, LeonVermeer, CeesSimes, Dina2022-06-28T13:56:22Z2022-04-272022-05-12T19:35:56Z2022-04-27T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.1/17888eng1422-006710.3390/ijms23094813info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-18T17:47:43Zoai:sapientia.ualg.pt:10400.1/17888Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T20:36:06.077026Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Nanoencapsulation of Gla-Rich Protein (GRP) as a novel approach to target inflammation |
title |
Nanoencapsulation of Gla-Rich Protein (GRP) as a novel approach to target inflammation |
spellingShingle |
Nanoencapsulation of Gla-Rich Protein (GRP) as a novel approach to target inflammation Viegas, Carla Nanoparticles Gla-rich protein (GRP) Chronic inflammatory diseases (CIDs) Inflammation Vitamin K-dependent protein (VKDP) |
title_short |
Nanoencapsulation of Gla-Rich Protein (GRP) as a novel approach to target inflammation |
title_full |
Nanoencapsulation of Gla-Rich Protein (GRP) as a novel approach to target inflammation |
title_fullStr |
Nanoencapsulation of Gla-Rich Protein (GRP) as a novel approach to target inflammation |
title_full_unstemmed |
Nanoencapsulation of Gla-Rich Protein (GRP) as a novel approach to target inflammation |
title_sort |
Nanoencapsulation of Gla-Rich Protein (GRP) as a novel approach to target inflammation |
author |
Viegas, Carla |
author_facet |
Viegas, Carla Araújo, Nuna Carreira, Joana Pontes, Jorge Filipe Macedo, Anjos L. Vinhas, Maurícia Moreira, Ana S. Faria, Tiago Q. Grenha, Ana de Matos, António A. Schurgers, Leon Vermeer, Cees Simes, Dina |
author_role |
author |
author2 |
Araújo, Nuna Carreira, Joana Pontes, Jorge Filipe Macedo, Anjos L. Vinhas, Maurícia Moreira, Ana S. Faria, Tiago Q. Grenha, Ana de Matos, António A. Schurgers, Leon Vermeer, Cees Simes, Dina |
author2_role |
author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Sapientia |
dc.contributor.author.fl_str_mv |
Viegas, Carla Araújo, Nuna Carreira, Joana Pontes, Jorge Filipe Macedo, Anjos L. Vinhas, Maurícia Moreira, Ana S. Faria, Tiago Q. Grenha, Ana de Matos, António A. Schurgers, Leon Vermeer, Cees Simes, Dina |
dc.subject.por.fl_str_mv |
Nanoparticles Gla-rich protein (GRP) Chronic inflammatory diseases (CIDs) Inflammation Vitamin K-dependent protein (VKDP) |
topic |
Nanoparticles Gla-rich protein (GRP) Chronic inflammatory diseases (CIDs) Inflammation Vitamin K-dependent protein (VKDP) |
description |
Chronic inflammation is a major driver of chronic inflammatory diseases (CIDs), with a tremendous impact worldwide. Besides its function as a pathological calcification inhibitor, vitamin K-dependent protein Gla-rich protein (GRP) was shown to act as an anti-inflammatory agent independently of its gamma-carboxylation status. Although GRP’s therapeutic potential has been highlighted, its low solubility at physiological pH still constitutes a major challenge for its biomedical application. In this work, we produced fluorescein-labeled chitosan-tripolyphosphate nanoparticles containing non-carboxylated GRP (ucGRP) (FCNG) via ionotropic gelation, increasing its bioavailability, stability, and anti-inflammatory potential. The results indicate the nanosized nature of FCNG with PDI and a zeta potential suitable for biomedical applications. FCNG’s anti-inflammatory activity was studied in macrophage-differentiated THP1 cells, and in primary vascular smooth muscle cells and chondrocytes, inflamed with LPS, TNFα and IL-1β, respectively. In all these in vitro human cell systems, FCNG treatments resulted in increased intra and extracellular GRP levels, and decreased pro-inflammatory responses of target cells, by decreasing pro-inflammatory cytokines and inflammation mediators. These results suggest the retained anti-inflammatory bioactivity of ucGRP in FCNG, strengthening the potential use of ucGRP as an anti-inflammatory agent with a wide spectrum of application, and opening up perspectives for its therapeutic application in CIDs. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-06-28T13:56:22Z 2022-04-27 2022-05-12T19:35:56Z 2022-04-27T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.1/17888 |
url |
http://hdl.handle.net/10400.1/17888 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
1422-0067 10.3390/ijms23094813 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
MDPI |
publisher.none.fl_str_mv |
MDPI |
dc.source.none.fl_str_mv |
reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia instacron:RCAAP |
instname_str |
FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
collection |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
repository.name.fl_str_mv |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
repository.mail.fl_str_mv |
info@rcaap.pt |
_version_ |
1833598740034748416 |