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Glucocorticoids Directly Affect Hyaluronan Production of Orbital Fibroblasts; A Potential Pleiotropic Effect in Graves’ Orbitopathy

Orbital connective tissue expansion is a hallmark of Graves’ orbitopathy (GO). In moderate-to-severe active GO, glucocorticoids (GC) are the first line of treatment. Here we show that hydrocortisone (HC), prednisolone (P), methylprednisolone (MP), and dexamethasone (DEX) inhibit the hyaluronan (HA)...

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Autores principales: Galgoczi, Erika, Katko, Monika, Papp, Fruzsina Reka, Csiki, Robert, Csiha, Sara, Erdei, Annamaria, Bodor, Miklos, Ujhelyi, Bernadett, Steiber, Zita, Gyory, Ferenc, Nagy, Endre V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9822010/
https://www.ncbi.nlm.nih.gov/pubmed/36615214
http://dx.doi.org/10.3390/molecules28010015
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author Galgoczi, Erika
Katko, Monika
Papp, Fruzsina Reka
Csiki, Robert
Csiha, Sara
Erdei, Annamaria
Bodor, Miklos
Ujhelyi, Bernadett
Steiber, Zita
Gyory, Ferenc
Nagy, Endre V.
author_facet Galgoczi, Erika
Katko, Monika
Papp, Fruzsina Reka
Csiki, Robert
Csiha, Sara
Erdei, Annamaria
Bodor, Miklos
Ujhelyi, Bernadett
Steiber, Zita
Gyory, Ferenc
Nagy, Endre V.
author_sort Galgoczi, Erika
collection PubMed
description Orbital connective tissue expansion is a hallmark of Graves’ orbitopathy (GO). In moderate-to-severe active GO, glucocorticoids (GC) are the first line of treatment. Here we show that hydrocortisone (HC), prednisolone (P), methylprednisolone (MP), and dexamethasone (DEX) inhibit the hyaluronan (HA) production of orbital (OF) and dermal (DF) fibroblasts. HA production of GO OFs (n = 4), NON-GO OFs (n = 4) and DFs (n = 4) was measured by ELISA. mRNA expression of enzymes of HA metabolism and fibroblast proliferation was examined by RT-PCR and BrdU incorporation, respectively. After 24 h of GC treatment (1µM) HA production decreased by an average of 67.9 ± 3.11% (p < 0.0001) in all cell cultures. HAS2, HAS3 and HYAL1 expression in OFs also decreased (p = 0.009, p = 0.0005 and p = 0.015, respectively). Ten ng/mL PDGF-BB increased HA production and fibroblast proliferation in all cell lines (p < 0.0001); GC treatment remained effective and reduced HA production under PDGF-BB-stimulated conditions (p < 0.0001). MP and DEX reduced (p < 0.001, p = 0.002, respectively) PDGF-BB-induced HAS2 expression in OFs. MP and DEX treatment decreased PDGF-BB stimulated HAS3 expression (p = 0.035 and p = 0.029, respectively). None of the GCs tested reduced the PDGF-BB stimulated proliferation rate. Our results confirm that GCs directly reduce the HA production of OFs, which may contribute to the beneficial effect of GCs in GO.
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spelling pubmed-98220102023-01-07 Glucocorticoids Directly Affect Hyaluronan Production of Orbital Fibroblasts; A Potential Pleiotropic Effect in Graves’ Orbitopathy Galgoczi, Erika Katko, Monika Papp, Fruzsina Reka Csiki, Robert Csiha, Sara Erdei, Annamaria Bodor, Miklos Ujhelyi, Bernadett Steiber, Zita Gyory, Ferenc Nagy, Endre V. Molecules Article Orbital connective tissue expansion is a hallmark of Graves’ orbitopathy (GO). In moderate-to-severe active GO, glucocorticoids (GC) are the first line of treatment. Here we show that hydrocortisone (HC), prednisolone (P), methylprednisolone (MP), and dexamethasone (DEX) inhibit the hyaluronan (HA) production of orbital (OF) and dermal (DF) fibroblasts. HA production of GO OFs (n = 4), NON-GO OFs (n = 4) and DFs (n = 4) was measured by ELISA. mRNA expression of enzymes of HA metabolism and fibroblast proliferation was examined by RT-PCR and BrdU incorporation, respectively. After 24 h of GC treatment (1µM) HA production decreased by an average of 67.9 ± 3.11% (p < 0.0001) in all cell cultures. HAS2, HAS3 and HYAL1 expression in OFs also decreased (p = 0.009, p = 0.0005 and p = 0.015, respectively). Ten ng/mL PDGF-BB increased HA production and fibroblast proliferation in all cell lines (p < 0.0001); GC treatment remained effective and reduced HA production under PDGF-BB-stimulated conditions (p < 0.0001). MP and DEX reduced (p < 0.001, p = 0.002, respectively) PDGF-BB-induced HAS2 expression in OFs. MP and DEX treatment decreased PDGF-BB stimulated HAS3 expression (p = 0.035 and p = 0.029, respectively). None of the GCs tested reduced the PDGF-BB stimulated proliferation rate. Our results confirm that GCs directly reduce the HA production of OFs, which may contribute to the beneficial effect of GCs in GO. MDPI 2022-12-20 /pmc/articles/PMC9822010/ /pubmed/36615214 http://dx.doi.org/10.3390/molecules28010015 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Galgoczi, Erika
Katko, Monika
Papp, Fruzsina Reka
Csiki, Robert
Csiha, Sara
Erdei, Annamaria
Bodor, Miklos
Ujhelyi, Bernadett
Steiber, Zita
Gyory, Ferenc
Nagy, Endre V.
Glucocorticoids Directly Affect Hyaluronan Production of Orbital Fibroblasts; A Potential Pleiotropic Effect in Graves’ Orbitopathy
title Glucocorticoids Directly Affect Hyaluronan Production of Orbital Fibroblasts; A Potential Pleiotropic Effect in Graves’ Orbitopathy
title_full Glucocorticoids Directly Affect Hyaluronan Production of Orbital Fibroblasts; A Potential Pleiotropic Effect in Graves’ Orbitopathy
title_fullStr Glucocorticoids Directly Affect Hyaluronan Production of Orbital Fibroblasts; A Potential Pleiotropic Effect in Graves’ Orbitopathy
title_full_unstemmed Glucocorticoids Directly Affect Hyaluronan Production of Orbital Fibroblasts; A Potential Pleiotropic Effect in Graves’ Orbitopathy
title_short Glucocorticoids Directly Affect Hyaluronan Production of Orbital Fibroblasts; A Potential Pleiotropic Effect in Graves’ Orbitopathy
title_sort glucocorticoids directly affect hyaluronan production of orbital fibroblasts; a potential pleiotropic effect in graves’ orbitopathy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9822010/
https://www.ncbi.nlm.nih.gov/pubmed/36615214
http://dx.doi.org/10.3390/molecules28010015
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