The role of extracellular vesicle miRNAs and tRNAs in synovial fibroblast senescence.
extracellular vescicles
miRNA
osteoarthiritis
senescence
synovial fibroblast
tRNA
Journal
Frontiers in molecular biosciences
ISSN: 2296-889X
Titre abrégé: Front Mol Biosci
Pays: Switzerland
ID NLM: 101653173
Informations de publication
Date de publication:
2022
2022
Historique:
received:
17
06
2022
accepted:
06
09
2022
entrez:
10
10
2022
pubmed:
11
10
2022
medline:
11
10
2022
Statut:
epublish
Résumé
Extracellular vesicles are mediators of intercellular communication with critical roles in cellular senescence and ageing. In arthritis, senescence is linked to the activation of a pro-inflammatory phenotype contributing to chronic arthritis pathogenesis. We hypothesised that senescent osteoarthritic synovial fibroblasts induce senescence and a pro-inflammatory phenotype in non-senescent osteoarthritic fibroblasts, mediated through extracellular vesicle cargo. Small RNA-sequencing and mass spectrometry proteomics were performed on extracellular vesicles isolated from the secretome of non-senescent and irradiation-induced senescent synovial fibroblasts. β-galactosidase staining confirmed senescence in SFs. RNA sequencing identified 17 differentially expressed miRNAs, 11 lncRNAs, 14 tRNAs and one snoRNA and, 21 differentially abundant proteins were identified by mass spectrometry. Bioinformatics analysis of miRNAs identified fibrosis, cell proliferation, autophagy, and cell cycle as significant pathways, tRNA analysis was enriched for signaling pathways including FGF, PI3K/AKT and MAPK, whilst protein analysis identified PAX3-FOXO1, MYC and TFGB1 as enriched upstream regulators involved in senescence and cell cycle arrest. Finally, treatment of non-senescent synovial fibroblasts with senescent extracellular vesicles confirmed the bystander effect, inducing senescence in non-senescent cells potentially through down regulation of NF-κβ and cAMP response element signaling pathways thus supporting our hypothesis. Understanding the exact composition of EV-derived small RNAs of senescent cells in this way will inform our understanding of their roles in inflammation, intercellular communication, and as active molecules in the senescence bystander effect.
Identifiants
pubmed: 36213127
doi: 10.3389/fmolb.2022.971621
pii: 971621
pmc: PMC9537453
doi:
Types de publication
Journal Article
Langues
eng
Pagination
971621Subventions
Organisme : Medical Research Council
ID : MR/P020941/1
Pays : United Kingdom
Informations de copyright
Copyright © 2022 Wijesinghe, Anderson, Brown, Nanus, Housmans, Green, Hackl, Choi, Arkill, Welting, James, Jones and Peffers.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Références
Cell Biosci. 2019 Feb 15;9:19
pubmed: 30815248
Arthritis Res Ther. 2014 Aug 04;16(4):R163
pubmed: 25092378
Genome Biol. 2009;10(3):R25
pubmed: 19261174
Nucleic Acids Res. 2004 Jan 1;32(Database issue):D109-11
pubmed: 14681370
Gene Regul Syst Bio. 2015 Sep 10;9:27-33
pubmed: 26401098
Nat Rev Rheumatol. 2019 Apr;15(4):191-192
pubmed: 30770908
Cell. 2007 Aug 24;130(4):638-50
pubmed: 17719542
Mol Cell Biol. 2019 May 28;39(12):
pubmed: 30988157
Nucleic Acids Res. 2019 Jan 8;47(D1):D442-D450
pubmed: 30395289
J Extracell Vesicles. 2018 Nov 23;7(1):1535750
pubmed: 30637094
J Clin Invest. 2018 Apr 2;128(4):1229-1237
pubmed: 29608139
FEBS Lett. 2012 Jul 30;586(16):2389-95
pubmed: 22677172
Sci Rep. 2019 May 14;9(1):7381
pubmed: 31089163
J Clin Endocrinol Metab. 2014 Oct;99(10):E1957-66
pubmed: 25029423
Immun Ageing. 2019 Nov 05;16:29
pubmed: 31708994
Tumour Biol. 2016 Oct;37(10):13077-13090
pubmed: 27596143
J Pain Res. 2021 Feb 04;14:297-310
pubmed: 33574696
Sci Rep. 2020 Aug 10;10(1):13426
pubmed: 32778764
Oncogene. 1997 Jul 10;15(2):179-92
pubmed: 9244353
Oncogene. 2018 Apr;37(15):1991-2007
pubmed: 29367756
Am J Transl Res. 2017 Jun 15;9(6):2852-2864
pubmed: 28670374
Sci Rep. 2016 Feb 04;6:20455
pubmed: 26842662
Malays Orthop J. 2019 Mar;13(1):1-7
pubmed: 31001376
Genome Biol. 2014;15(12):550
pubmed: 25516281
Cancer Res. 2007 Jul 15;67(14):6691-9
pubmed: 17638879
Nucleic Acids Res. 2012 Jan;40(1):37-52
pubmed: 21911355
Stem Cells Dev. 2012 Jul 1;21(10):1749-60
pubmed: 21988232
Neurobiol Stress. 2021 Jul 29;15:100371
pubmed: 34458511
Mech Ageing Dev. 2018 Mar;170:30-36
pubmed: 28837845
Aging (Albany NY). 2020 Aug 15;12(15):15756-15770
pubmed: 32805717
EBioMedicine. 2021 Oct;72:103618
pubmed: 34628351
Biochem Pharmacol. 2012 Jun 1;83(11):1484-94
pubmed: 22230477
Nat Methods. 2012 Jun 28;9(7):676-82
pubmed: 22743772
Nat Rev Rheumatol. 2021 Jan;17(1):47-57
pubmed: 33208917
Int J Mol Sci. 2022 Jan 22;23(3):
pubmed: 35163149
Nucleic Acids Res. 2019 Jan 8;47(D1):D1250-D1251
pubmed: 30535383
Arthritis Rheumatol. 2020 Apr;72(4):609-619
pubmed: 31682073
Bioinformatics. 2016 Oct 1;32(19):3047-8
pubmed: 27312411
JACC Basic Transl Sci. 2020 Jan 15;5(2):148-166
pubmed: 32140622
Bioinformatics. 2010 Jan 1;26(1):139-40
pubmed: 19910308
Cold Spring Harb Perspect Biol. 2017 Apr 3;9(4):
pubmed: 27920038
Aging Cell. 2019 Feb;18(1):e12848
pubmed: 30462359
J Autoimmun. 2018 May;89:162-170
pubmed: 29371048
Mol Ther. 2017 Mar 1;25(3):715-727
pubmed: 28139355
Nucleic Acids Res. 2018 Jan 4;46(D1):D754-D761
pubmed: 29155950
Front Cell Dev Biol. 2021 Mar 29;9:645593
pubmed: 33855023
PLoS One. 2010 Sep 01;5(9):
pubmed: 20824140
Cell Death Differ. 2012 Apr;19(4):713-21
pubmed: 22052189
Front Immunol. 2020 Aug 18;11:1757
pubmed: 33013829
J Invest Dermatol. 2021 Apr;141(4S):1076-1086.e3
pubmed: 33279585