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Tytuł pozycji:

Circ-SPG11 knockdown hampers IL-1β-induced osteoarthritis progression via targeting miR-337-3p/ADAMTS5.

Tytuł:
Circ-SPG11 knockdown hampers IL-1β-induced osteoarthritis progression via targeting miR-337-3p/ADAMTS5.
Autorzy:
Liu Y; Department of Orthopedics, Shijiazhuang People's Hospital, No. 365 Jianhua South Road, Shijiazhang, Hebei, 050000, People's Republic of China.
Li Q; Department of Orthopedics, Shijiazhuang People's Hospital, No. 365 Jianhua South Road, Shijiazhang, Hebei, 050000, People's Republic of China.
Gao Z; Department of Orthopedics, Shijiazhuang People's Hospital, No. 365 Jianhua South Road, Shijiazhang, Hebei, 050000, People's Republic of China.
Lei F; Department of Orthopedics, Shijiazhuang People's Hospital, No. 365 Jianhua South Road, Shijiazhang, Hebei, 050000, People's Republic of China. .
Gao X; Department of Orthopedics, Shijiazhuang People's Hospital, No. 365 Jianhua South Road, Shijiazhang, Hebei, 050000, People's Republic of China.
Źródło:
Journal of orthopaedic surgery and research [J Orthop Surg Res] 2021 Jun 17; Vol. 16 (1), pp. 392. Date of Electronic Publication: 2021 Jun 17.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: London : BioMed Central, 2006-
MeSH Terms:
Gene Knockdown Techniques*
ADAMTS5 Protein/*genetics
ADAMTS5 Protein/*metabolism
Interleukin-1beta/*adverse effects
MicroRNAs/*genetics
MicroRNAs/*metabolism
Osteoarthritis, Knee/*genetics
Proteins/*genetics
RNA, Circular/*genetics
Cell Line ; Disease Progression ; Down-Regulation/genetics ; Gene Expression Regulation/genetics ; Humans ; Osteoarthritis, Knee/etiology ; Proteins/physiology ; RNA, Circular/physiology ; Up-Regulation/genetics
References:
Semin Arthritis Rheum. 2013 Dec;43(3):303-13. (PMID: 23992801)
Life Sci. 2019 Dec 15;239:116984. (PMID: 31647948)
Life Sci. 2020 Sep 1;256:117924. (PMID: 32522568)
Osteoarthritis Cartilage. 2013 Oct;21(10):1436-42. (PMID: 23774472)
Stem Cell Res Ther. 2016 Dec 1;7(1):180. (PMID: 27906093)
Ageing Res Rev. 2017 Nov;40:20-30. (PMID: 28774716)
Ann Intern Med. 2014 Jul 1;161(1):ITC1-16. (PMID: 24979462)
J Orthop Res. 2018 Feb;36(2):699-710. (PMID: 29058776)
Sci Rep. 2016 Mar 02;6:22572. (PMID: 26931159)
Nat Rev Rheumatol. 2016 Jul;12(7):412-20. (PMID: 27192932)
Bull World Health Organ. 2003;81(9):646-56. (PMID: 14710506)
Int J Mol Med. 2016 Feb;37(2):509-16. (PMID: 26707794)
Mol Cancer. 2017 Sep 11;16(1):151. (PMID: 28893265)
Lancet. 2015 Jul 25;386(9991):376-87. (PMID: 25748615)
Biomed Pharmacother. 2017 Nov;95:1194-1200. (PMID: 28931211)
Hum Cell. 2017 Oct;30(4):311-318. (PMID: 28795385)
Cell Cycle. 2020 Jul;19(13):1696-1705. (PMID: 32476580)
Autophagy. 2017 Oct 3;13(10):1722-1741. (PMID: 28786753)
Gene. 2018 Mar 10;646:203-209. (PMID: 29305974)
Ann Rheum Dis. 2014 Sep;73(9):1659-64. (PMID: 23744977)
Eur Rev Med Pharmacol Sci. 2020 Mar;24(5):2585-2600. (PMID: 32196629)
J Biotechnol. 2016 Nov 20;238:42-51. (PMID: 27671698)
J Inflamm (Lond). 2020 Feb 18;17:8. (PMID: 32099534)
Instr Course Lect. 2005;54:465-80. (PMID: 15952258)
Yonsei Med J. 2019 Nov;60(11):1081-1092. (PMID: 31637891)
Mol Ther. 2019 Mar 6;27(3):531-541. (PMID: 30692016)
Biomed Pharmacother. 2020 Apr;124:109828. (PMID: 31986409)
Gene. 2018 Feb 20;644:20-26. (PMID: 29247798)
Cell Biol Int. 2017 Dec;41(12):1283-1289. (PMID: 28276108)
Cancer Lett. 2015 Sep 1;365(2):141-8. (PMID: 26052092)
Ann Rheum Dis. 2019 Jun;78(6):826-836. (PMID: 30923232)
Gastric Cancer. 2020 May;23(3):437-448. (PMID: 31776711)
Contributed Indexing:
Keywords: ADAMTS5; Circ-SPG11; IL-1β; MiR-337-3p; Osteoarthritis
Substance Nomenclature:
0 (Interleukin-1beta)
0 (MicroRNAs)
0 (Mirn337 microRNA, human)
0 (Proteins)
0 (RNA, Circular)
0 (SPG11 protein, human)
EC 3.4.24.- (ADAMTS5 Protein)
EC 3.4.24.- (ADAMTS5 protein, human)
Entry Date(s):
Date Created: 20210618 Date Completed: 20211110 Latest Revision: 20211110
Update Code:
20240104
PubMed Central ID:
PMC8212518
DOI:
10.1186/s13018-021-02526-y
PMID:
34140036
Czasopismo naukowe
Background: Osteoarthritis (OA) is responsible for the impotent disability in old people. Circular RNA (circRNA) has been reported to be related to the development of diseases. The lack of research on the role of circRNA spastic paraplegia 11 (circ-SPG11) results in conducting this study.
Methods: The expression of circ-SPG11, microRNA-337-3p (miR-337-3p), and aggrecanases like a disintegrin and metalloproteinase with thrombospondin motifs 5 (ADAMTS5) mRNA was detected by quantitative real-time polymerase chain reaction (qRT-PCR). Western blot was used to measure the protein expression of extracellular matrix (ECM) degradation-related markers and ADAMTS5. Ribonuclease R (RNase R) was applied to test the stability of circ-SPG11 in CHON-001 cells. The viability, apoptosis, TNF-α and IL-6 production were determined by cell counting kit-8 (CCK-8) assay, flow cytometry assay, and enzyme-linked immunosorbent assay (ELISA), respectively. Meanwhile, the interaction between miR-337-3p and circ-SPG11 or ADAMTS5 was respectively predicted by Circinteractome or Starbase2.0, which was further verified by dual-luciferase reporter system and RNA binding protein immunoprecipitation (RIP) assay.
Results: Circ-SPG11 and ADAMTS5 were upregulated and miR-337-3p was downregulated in OA tissues and OA model cells. Circ-SPG11 knockdown allayed interleukin 1β (IL-1β)-induced restraint in viability and promotion in apoptosis, TNF-α, and IL-6 generation and ECM degradation in CHON-001 cells. Anti-miR-337-3p or ADAMTS5 overexpression correspondingly reversed si-circ-SPG11 or miR-337-3p overexpression-mediated facilitation in viability, and inhibition in apoptosis, TNF-α and IL-6 generation and ECM degradation in OA model cells. Moreover, anti-miR-337-3p ameliorated si-circ-SPG11-mediated inhibition in ADAMTS5 mRNA and protein expression in OA model cells.
Conclusion: Circ-SPG11 facilitated OA development via regulating miR-337-3p/ADAMTS5 axis. This finding might contribute to the improvement of OA therapy.

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