Cargando…

Fibroblast-Like Synoviocytes Glucose Metabolism as a Therapeutic Target in Rheumatoid Arthritis

Metabolomic studies show that rheumatoid arthritis (RA) is associated with metabolic disruption that may be therapeutically targetable. Among them, glucose metabolism and glycolytic intermediaries seem to have an important role in fibroblast-like synoviocytes (FLS) phenotype and might contribute to...

Descripción completa

Detalles Bibliográficos
Autores principales: de Oliveira, Patricia Gnieslaw, Farinon, Mirian, Sanchez-Lopez, Elsa, Miyamoto, Shigeki, Guma, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688519/
https://www.ncbi.nlm.nih.gov/pubmed/31428089
http://dx.doi.org/10.3389/fimmu.2019.01743
_version_ 1783442899621380096
author de Oliveira, Patricia Gnieslaw
Farinon, Mirian
Sanchez-Lopez, Elsa
Miyamoto, Shigeki
Guma, Monica
author_facet de Oliveira, Patricia Gnieslaw
Farinon, Mirian
Sanchez-Lopez, Elsa
Miyamoto, Shigeki
Guma, Monica
author_sort de Oliveira, Patricia Gnieslaw
collection PubMed
description Metabolomic studies show that rheumatoid arthritis (RA) is associated with metabolic disruption that may be therapeutically targetable. Among them, glucose metabolism and glycolytic intermediaries seem to have an important role in fibroblast-like synoviocytes (FLS) phenotype and might contribute to early stage disease pathogenesis. RA FLS are transformed from quiescent to aggressive and metabolically active cells and several works have shown that glucose metabolism is increased in activated FLS. Glycolytic inhibitors reduce not only FLS aggressive phenotype in vitro but also decrease bone and cartilage damage in several murine models of arthritis. Essential glycolytic enzymes, including hexokinase 2 (HK2) and 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase (PFKFB) enzymes, have important roles in FLS behavior. Of interest, HK2 is an inducible enzyme present only in the inflamed rheumatic tissues compared to osteoarthritis synovium. It is a contributor to glucose metabolism that could be selectively targeted without compromising systemic homeostasis as a novel approach for combination therapy independent of systemic immunosuppression. More information about metabolic targets that do not compromise global glucose metabolism in normal cells is needed.
format Online
Article
Text
id pubmed-6688519
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-66885192019-08-19 Fibroblast-Like Synoviocytes Glucose Metabolism as a Therapeutic Target in Rheumatoid Arthritis de Oliveira, Patricia Gnieslaw Farinon, Mirian Sanchez-Lopez, Elsa Miyamoto, Shigeki Guma, Monica Front Immunol Immunology Metabolomic studies show that rheumatoid arthritis (RA) is associated with metabolic disruption that may be therapeutically targetable. Among them, glucose metabolism and glycolytic intermediaries seem to have an important role in fibroblast-like synoviocytes (FLS) phenotype and might contribute to early stage disease pathogenesis. RA FLS are transformed from quiescent to aggressive and metabolically active cells and several works have shown that glucose metabolism is increased in activated FLS. Glycolytic inhibitors reduce not only FLS aggressive phenotype in vitro but also decrease bone and cartilage damage in several murine models of arthritis. Essential glycolytic enzymes, including hexokinase 2 (HK2) and 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase (PFKFB) enzymes, have important roles in FLS behavior. Of interest, HK2 is an inducible enzyme present only in the inflamed rheumatic tissues compared to osteoarthritis synovium. It is a contributor to glucose metabolism that could be selectively targeted without compromising systemic homeostasis as a novel approach for combination therapy independent of systemic immunosuppression. More information about metabolic targets that do not compromise global glucose metabolism in normal cells is needed. Frontiers Media S.A. 2019-08-02 /pmc/articles/PMC6688519/ /pubmed/31428089 http://dx.doi.org/10.3389/fimmu.2019.01743 Text en Copyright © 2019 de Oliveira, Farinon, Sanchez-Lopez, Miyamoto and Guma. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
de Oliveira, Patricia Gnieslaw
Farinon, Mirian
Sanchez-Lopez, Elsa
Miyamoto, Shigeki
Guma, Monica
Fibroblast-Like Synoviocytes Glucose Metabolism as a Therapeutic Target in Rheumatoid Arthritis
title Fibroblast-Like Synoviocytes Glucose Metabolism as a Therapeutic Target in Rheumatoid Arthritis
title_full Fibroblast-Like Synoviocytes Glucose Metabolism as a Therapeutic Target in Rheumatoid Arthritis
title_fullStr Fibroblast-Like Synoviocytes Glucose Metabolism as a Therapeutic Target in Rheumatoid Arthritis
title_full_unstemmed Fibroblast-Like Synoviocytes Glucose Metabolism as a Therapeutic Target in Rheumatoid Arthritis
title_short Fibroblast-Like Synoviocytes Glucose Metabolism as a Therapeutic Target in Rheumatoid Arthritis
title_sort fibroblast-like synoviocytes glucose metabolism as a therapeutic target in rheumatoid arthritis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688519/
https://www.ncbi.nlm.nih.gov/pubmed/31428089
http://dx.doi.org/10.3389/fimmu.2019.01743
work_keys_str_mv AT deoliveirapatriciagnieslaw fibroblastlikesynoviocytesglucosemetabolismasatherapeutictargetinrheumatoidarthritis
AT farinonmirian fibroblastlikesynoviocytesglucosemetabolismasatherapeutictargetinrheumatoidarthritis
AT sanchezlopezelsa fibroblastlikesynoviocytesglucosemetabolismasatherapeutictargetinrheumatoidarthritis
AT miyamotoshigeki fibroblastlikesynoviocytesglucosemetabolismasatherapeutictargetinrheumatoidarthritis
AT gumamonica fibroblastlikesynoviocytesglucosemetabolismasatherapeutictargetinrheumatoidarthritis