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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  • Κοινότητες & Συλλογές
  • Ανά ημερομηνία δημοσίευσης
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The synergistic function of miR-140–5p and miR-146a on TLR4-mediated cytokine secretion in osteoarthritic chondrocytes

Thumbnail
Συγγραφέας
Papathanasiou I., Balis C., Trachana V., Mourmoura E., Tsezou A.
Ημερομηνία
2020
Γλώσσα
en
DOI
10.1016/j.bbrc.2019.11.168
Λέξη-κλειδί
immunoglobulin enhancer binding protein
interleukin 1beta
interleukin 6
microRNA
microRNA 140 5p
microRNA 146a
toll like receptor 4
tumor necrosis factor
unclassified drug
cytokine
microRNA
Mirn140 microRNA, human
MIRN146 microRNA, human
TLR4 protein, human
toll like receptor 4
aged
Article
bioinformatics
cell protection
chondrocyte
clinical article
controlled study
cytokine release
female
gene interaction
gene overexpression
gene targeting
genetic association
human
human cell
human tissue
inflammation
osteoarthritis
pathogenesis
priority journal
protein expression
protein phosphorylation
cell culture
chondrocyte
gene expression regulation
genetics
immunology
male
metabolism
middle aged
osteoarthritis
protein analysis
upregulation
Aged
Cells, Cultured
Chondrocytes
Cytokines
Female
Gene Expression Regulation
Humans
Inflammation
Male
MicroRNAs
Middle Aged
Osteoarthritis
Protein Interaction Maps
Toll-Like Receptor 4
Up-Regulation
Elsevier B.V.
Εμφάνιση Μεταδεδομένων
Επιτομή
ΜiR-140–5p and miR-146a regulate inflammatory pathways including TLR4/NF-κB signaling and have been found to be involved in OA pathogenesis. In this study, we investigated the effect of the synergistic function of miR-140–5p and miR-146a on inflammation mediated by TLR4 in ΟΑ chondrocytes. Bioinformatics analysis revealed that TLR4 was the only common OA-related target gene of miR-140–5p and miR-146a, located in the sub-network with the highest MCODE score; it also showed that the target genes of miR-140-5p and miR-146a which located in MCODE sub-networks were enriched in OA-related biological processes and pathways. Overexpression of miR-140–5p or miR-146a and combined miR-140–5p/miR-146a overexpression in OA chondrocytes demonstrated that combined treatment had the strongest negative effect on TLR4 expression. Moreover, simultaneous overexpression of miR-140–5p and miR-146a resulted in the highest reduction of NF-κΒ phosphorylation levels, as well as IL-1b, IL-6 and TNFa expression levels in OA chondrocytes as compared to the reductions observed when either miR-140-5p or miR-146a was overexpressed. Our results, therefore, demonstrate for the first time, that the synergistic function of miR-140–5p and miR-146a have a strong protective effect against inflammatory mediators’ production in OA chondrocytes through targeting the TLR4/NF-κB signaling. © 2019 Elsevier Inc.
URI
http://hdl.handle.net/11615/77832
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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