NODES_Inndiana_Z63_IN VITRO STUDY OF STORE-OPERATED CALCIUM ENTRY (SOCE) NEGATIVE MODULATORS ON VIABILITY, APOPTOSIS, AND CYTOKINE SECRETION OF HUMAN SYNOVIAL FIBROBLASTS

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Autore principale: Cappellano, Giuseppe
Natura: Recurso digital
Lingua:inglese
Pubblicazione: Zenodo 2024
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author Cappellano, Giuseppe
author_facet Cappellano, Giuseppe
contents <p>Osteoarthritis (OA) is a major cause of chronic pain and joint damage, involving low-grade synovitis that contributes to disease progression. Fibroblast-like synoviocytes (FLSs) are central to this process, producing inflammatory cytokines regulated by calcium (Ca2+) signaling. Targeting Ca2+ signaling through store-operated calcium entry (SOCE) could help reduce inflammation in OA.We  tested two novel SOCE-negative modulators (CIC-39 and BIP-26) and two drugs (methotrexate and celecoxib) on inflamed OA-FLSs. CIC-39 and BIP-26 reduced Ca2+ influx without affecting cell morphology or viability. Methotrexate and the SOCE modulators showed trends toward reducing cytokine expression, though results were not statistically significant. Celecoxib induced cell death in a dose-dependent manner and caused cell cycle arrest. Overall, SOCE modulators show potential as a new treatment strategy for OA.</p>
format Recurso digital
id zenodo_https___doi_org_10_5281_zenodo_13835778
institution Zenodo
language eng
publishDate 2024
publisher Zenodo
record_format zenodo
spellingShingle NODES_Inndiana_Z63_IN VITRO STUDY OF STORE-OPERATED CALCIUM ENTRY (SOCE) NEGATIVE MODULATORS ON VIABILITY, APOPTOSIS, AND CYTOKINE SECRETION OF HUMAN SYNOVIAL FIBROBLASTS
Cappellano, Giuseppe
Spoke 5 - Industry for Health and Silver Economy
INNDIANA Project
Eco healthcare
ECS00000036
<p>Osteoarthritis (OA) is a major cause of chronic pain and joint damage, involving low-grade synovitis that contributes to disease progression. Fibroblast-like synoviocytes (FLSs) are central to this process, producing inflammatory cytokines regulated by calcium (Ca2+) signaling. Targeting Ca2+ signaling through store-operated calcium entry (SOCE) could help reduce inflammation in OA.We  tested two novel SOCE-negative modulators (CIC-39 and BIP-26) and two drugs (methotrexate and celecoxib) on inflamed OA-FLSs. CIC-39 and BIP-26 reduced Ca2+ influx without affecting cell morphology or viability. Methotrexate and the SOCE modulators showed trends toward reducing cytokine expression, though results were not statistically significant. Celecoxib induced cell death in a dose-dependent manner and caused cell cycle arrest. Overall, SOCE modulators show potential as a new treatment strategy for OA.</p>
title NODES_Inndiana_Z63_IN VITRO STUDY OF STORE-OPERATED CALCIUM ENTRY (SOCE) NEGATIVE MODULATORS ON VIABILITY, APOPTOSIS, AND CYTOKINE SECRETION OF HUMAN SYNOVIAL FIBROBLASTS
topic Spoke 5 - Industry for Health and Silver Economy
INNDIANA Project
Eco healthcare
ECS00000036
url https://doi.org/10.5281/zenodo.13835778