Exploring the Impact of TLR-2 Signaling on miRNA Dysregulation in Intervertebral Disc Degeneration. (Record no. 14223)

MARC details
000 -LEADER
fixed length control field 02965nam a22003377a 4500
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fixed length control field 240723s20242024 xxu||||| |||| 00| 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 2701-0198
040 ## - CATALOGING SOURCE
Original cataloging agency Ovid MEDLINE(R)
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
PMID 38419396
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Title Exploring the Impact of TLR-2 Signaling on miRNA Dysregulation in Intervertebral Disc Degeneration.
251 ## - Source
Source Advances in Biology Online. :e2300581, 2024 Feb 28
252 ## - Abbreviated Source
Abbreviated source adv. biol. :e2300581, 2024 Feb 28
253 ## - Journal Name
Journal name Advanced biology
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Year 2024
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Publication date 2024 Feb 28
265 ## - SOURCE FOR ACQUISITION/SUBSCRIPTION ADDRESS [OBSOLETE]
Publication status aheadofprint
265 ## - SOURCE FOR ACQUISITION/SUBSCRIPTION ADDRESS [OBSOLETE]
Medline status Publisher
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Date added to catalog 2024-07-23
520 ## - SUMMARY, ETC.
Abstract Toll-like receptors (TLRs) are key mediators of inflammation in intervertebral disc (IVD) degeneration. TLR-2 activation contributes to the degenerative process by increasing the expression of extracellular matrix-degrading enzymes, pro-inflammatory cytokines, and neurotrophins. As potent post-transcriptional regulators, microRNAs can modulate intracellular mechanisms, and their dysregulation is known to contribute to numerous pathologies. This study aims to investigate the impact of TLR-2 signaling on miRNA dysregulation in the context of IVD degeneration. Small-RNA sequencing of degenerated IVD cells shows the dysregulation of ten miRNAs following TLR-2 activation by PAM2CSK4. The miR-155-5p is most significantly upregulated in degenerated and non-degenerated annulus fibrosus and nucleus pulposus cells. Sequence-based target and pathway prediction shows the involvement of miR-155-5p in inflammation- and cell fate-related pathways and TLR-2-induced miR-155-5p expression leads to the downregulation of its target c-FOS. Furthermore, changes specific to the activation of TLR-2 through fragmented fibronectin are seen in miR-484 and miR-487. Lastly, miR-100-3p, miR-320b, and miR-181a-3p expression exhibit degeneration-dependent changes. These results show that TLR-2 signaling leads to the dysregulation of miRNAs in IVD cells as well as their possible downstream effects on inflammation and degeneration. The identified miRNAs provide important opportunities as potential therapeutic targets for IVD degeneration and low back pain. Copyright © 2024 The Authors. Advanced Biology published by Wiley-VCH GmbH.
546 ## - LANGUAGE NOTE
Language note English
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Indexing Automated
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element IN PROCESS -- NOT YET INDEXED
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Institution MedStar Washington Hospital Center
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Department Orthopedic Surgery
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Medline publication type Journal Article
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Local Authors Mesfin, Addisu
Institution Code MWHC
790 ## - Authors
All authors Cazzanelli P, Lamoca M, Hausmann ON, Mesfin A, Puvanesarajah V, Hitzl W, Haglund L, Wuertz-Kozak K
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DOI <a href="https://dx.doi.org/10.1002/adbi.202300581">https://dx.doi.org/10.1002/adbi.202300581</a>
Public note https://dx.doi.org/10.1002/adbi.202300581
858 ## - ORCID
ORCID text Cazzanelli, Petra
Orcid <a href="https://orcid.org/0009-0007-3114-951XI - Wuertz-Kozak, Karin">https://orcid.org/0009-0007-3114-951XI - Wuertz-Kozak, Karin</a>
-- <a href="https://orcid.org/0000-0002-3281-4629">https://orcid.org/0000-0002-3281-4629</a>
Name https://orcid.org/0009-0007-3114-951XI - Wuertz-Kozak, Karin
-- https://orcid.org/0000-0002-3281-4629
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Journal Article
Item type description Article
Holdings
Withdrawn status Lost status Damaged status Not for loan Collection Home library Current library Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
              07/23/2024   38419396 38419396 07/23/2024 07/23/2024 Journal Article

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