Characterization of exosomal long non-coding RNAs in chondrogenic differentiation of human adipose-derived stem cells.


Journal

Molecular and cellular biochemistry
ISSN: 1573-4919
Titre abrégé: Mol Cell Biochem
Pays: Netherlands
ID NLM: 0364456

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 12 06 2020
accepted: 24 11 2020
pubmed: 4 1 2021
medline: 3 8 2021
entrez: 3 1 2021
Statut: ppublish

Résumé

The exosomes derived from chondrogenic stem cells and long non-coding RNAs (lncRNAs) play a key role in cartilage regeneration. Here, we investigated the expression profile of exosomal lncRNAs in chondrogenesis of human adipose derived stem cells (hADSCs). hADSCs were induced to differentiate into chondrocytes in vitro. Exosomes from undifferentiated hADSCs and chondrogenic hADSCs were isolated. LncRNA and mRNA expression profiles in the isolated exosomes were analyzed by RNA sequencing. The resultant data were subjected to gene ontology (GO) terms and KEGG pathway analysis to identify differentially expressed lncRNAs. We identified 23 upregulated and 163 downregulated lncRNAs in exosomes derived from chondrogenic hADSCs compared to that in exosomes from undifferentiated hADSCs. In addition, analysis of mRNA expression data revealed 968 upregulated genes and 572 downregulated genes in exosomes of chondrogenic hADSCs. Lncrna and mRNA expression levels were further validated by qRT-PCR. Differentially expressed lncRNAs and mRNAs were utilized to construct a coding-non-coding gene co-expression network (CNC network). GO terms and KEGG pathway enrichment analysis revealed several significant processes differentially regulated between undifferentiated hADSCs and chondrogenic hADSCs. Taken together, this study revealed the differential expression of exosomal lncRNAs of chondrogenic hADSCs and provided a foundation for future study on the cartilage recovery mechanism of exosomes derived from chondrogenic stem cells.

Identifiants

pubmed: 33389494
doi: 10.1007/s11010-020-04003-2
pii: 10.1007/s11010-020-04003-2
doi:

Substances chimiques

MicroRNAs 0
RNA, Long Noncoding 0
RNA, Messenger 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1411-1420

Subventions

Organisme : National Natural Science Foundation of China
ID : 81874014
Organisme : National Natural Science Foundation of China
ID : 81672198
Organisme : National Natural Science Foundation of China
ID : 81802187
Organisme : Natural Science Foundation of Guangdong Province
ID : 2018030310355

Références

Loeser RF, Goldring SR, Scanzello CR, Goldring MB (2012) Osteoarthritis: a disease of the joint as an organ. Arthritis Rheum 64:1697–1707. https://doi.org/10.1002/art.34453
doi: 10.1002/art.34453 pubmed: 22392533 pmcid: 3366018
Mercer TR, Dinger ME, Mattick JS (2009) Long non-coding RNAs: insights into functions. Nat Rev Genet 10:155–159. https://doi.org/10.1038/nrg2521
doi: 10.1038/nrg2521 pubmed: 19188922
Jiang S, Lu J, Deng Z, Li Y, Lei G (2017) Long noncoding RNAs in osteoarthritis. Joint Bone Spine 84:553–556. https://doi.org/10.1016/j.jbspin.2016.09.006
doi: 10.1016/j.jbspin.2016.09.006 pubmed: 27919571
Cen X, Huang X, Sun W, Liu Q, Liu J (2017) Long noncoding RNAs: a new regulatory code in osteoarthritis. Am J Transl Res 9:4747
pubmed: 29218077 pmcid: 5714763
Li Y, Li Z, Li C, Zeng Y, Liu Y (2019) Long noncoding RNA TM1P3 is involved in osteoarthritis by mediating chondrocyte extracellular matrix degradation. J Cell Biochem. https://doi.org/10.1002/jcb.28539
doi: 10.1002/jcb.28539 pubmed: 31886586 pmcid: 7808212
Gao GC, Cheng XG, Wei QQ, Chen WC, Huang WZ (2019) Long noncoding RNA MALAT-1 inhibits apoptosis and matrix metabolism disorder in interleukin-1beta-induced inflammation in articular chondrocytes via the JNK signaling pathway. J Cell Biochem. https://doi.org/10.1002/jcb.28977
doi: 10.1002/jcb.28977 pubmed: 31886580 pmcid: 6771484
Thery C (2011) Exosomes: secreted vesicles and intercellular communications. F1000 Biol Rep 3:15. https://doi.org/10.3410/B3-15
doi: 10.3410/B3-15 pubmed: 21876726 pmcid: 3155154
Familtseva A, Jeremic N, Tyagi SC (2019) Exosomes: cell-created drug delivery systems. Mol Cell Biochem 459:1–6. https://doi.org/10.1007/s11010-019-03545-4
doi: 10.1007/s11010-019-03545-4 pubmed: 31073888
Nabet BY, Qiu Y, Shabason JE et al (2017) Exosome RNA unshielding couples stromal activation to pattern recognition receptor signaling in cancer. Cell 170:352–366. https://doi.org/10.1016/j.cell.2017.06.031
doi: 10.1016/j.cell.2017.06.031 pubmed: 28709002 pmcid: 6611169
Bang C, Thum T (2012) Exosomes: new players in cell-cell communication. Int J Biochem Cell Biol 44:2060–2064. https://doi.org/10.1016/j.biocel.2012.08.007
doi: 10.1016/j.biocel.2012.08.007
Zhang S, Chu WC, Lai RC et al (2016) Exosomes derived from human embryonic mesenchymal stem cells promote osteochondral regeneration. Osteoarthr Cartil 24:2135–2140. https://doi.org/10.1016/j.joca.2016.06.022
doi: 10.1016/j.joca.2016.06.022
Toh WS, Lai RC, Hui JHP, Lim SK (2017) MSC exosome as a cell-free MSC therapy for cartilage regeneration: implications for osteoarthritis treatment. Semin Cell Dev Biol 67:56–64. https://doi.org/10.1016/j.semcdb.2016.11.008
doi: 10.1016/j.semcdb.2016.11.008 pubmed: 27871993
Vonk LA, van Dooremalen S, Liv N et al (2018) Mesenchymal stromal/stem cell-derived extracellular vesicles promote human cartilage regeneration in vitro. Theranostics 8:906–920. https://doi.org/10.7150/thno.20746
doi: 10.7150/thno.20746 pubmed: 29463990 pmcid: 5817101
Liu Y, Zou R, Wang Z et al (2018) Exosomal KLF3-AS1 from hMSCs promoted cartilage repair and chondrocyte proliferation in osteoarthritis. Biochem J 475:3629–3638. https://doi.org/10.1042/BCJ20180675
doi: 10.1042/BCJ20180675 pubmed: 30341166
Tao S, Yuan T, Zhang Y et al (2017) Exosomes derived from miR-140-5p-overexpressing human synovial mesenchymal stem cells enhance cartilage tissue regeneration and prevent osteoarthritis of the knee in a rat model. Theranostics 7:180–195. https://doi.org/10.7150/thno.17133
doi: 10.7150/thno.17133 pubmed: 28042326 pmcid: 5196895
Sun H, Hu S, Zhang Z et al (2019) Expression of exosomal microRNAs during chondrogenic differentiation of human bone mesenchymal stem cells. J Cell Biochem 120:171–181. https://doi.org/10.1002/jcb.27289
doi: 10.1002/jcb.27289 pubmed: 30277597
Zhang Z, Zhang H, Kang Y et al (2012) miRNA expression profile during osteogenic differentiation of human adipose-derived stem cells. J Cell Biochem 113:888–898. https://doi.org/10.1002/jcb.23418
doi: 10.1002/jcb.23418 pubmed: 22371969
Zhang Z, Kang Y, Zhang Z et al (2012) Expression of microRNAs during chondrogenesis of human adipose-derived stem cells. Osteoarthr Cartil 20:1638–1646. https://doi.org/10.1016/j.joca.2012.08.024
doi: 10.1016/j.joca.2012.08.024
Hu S, Mao G, Zhang Z et al (2019) MicroRNA-320c inhibits development of osteoarthritis through downregulation of canonical Wnt signaling pathway. Life Sci 228:242–250. https://doi.org/10.1016/j.lfs.2019.05.011
doi: 10.1016/j.lfs.2019.05.011 pubmed: 31075235
Xia B, Chen Di, Zhang J et al (2014) Osteoarthritis pathogenesis: a review of molecular mechanisms. Calcif Tissue Int 95:495–505. https://doi.org/10.1007/s00223-014-9917-9
doi: 10.1007/s00223-014-9917-9 pubmed: 25311420 pmcid: 4747051
Zhang S, Chuah SJ, Lai RC et al (2018) MSC exosomes mediate cartilage repair by enhancing proliferation, attenuating apoptosis and modulating immune reactivity. Biomaterials 156:16–27. https://doi.org/10.1016/j.biomaterials.2017.11.028
doi: 10.1016/j.biomaterials.2017.11.028 pubmed: 29182933
Zhang S, Teo K, Chuah SJ et al (2019) MSC exosomes alleviate temporomandibular joint osteoarthritis by attenuating inflammation and restoring matrix homeostasis. Biomaterials 200:35–47. https://doi.org/10.1016/j.biomaterials.2019.02.006
doi: 10.1016/j.biomaterials.2019.02.006 pubmed: 30771585
Wang KC, Chang HY (2011) Molecular mechanisms of long noncoding RNAs. Mol Cell 43:904–914. https://doi.org/10.1016/j.molcel.2011.08.018
doi: 10.1016/j.molcel.2011.08.018 pubmed: 21925379 pmcid: 3199020
Pearson MJ, Jones SW (2016) Review: long noncoding RNAs in the regulation of inflammatory pathways in rheumatoid arthritis and osteoarthritis. Arthritis Rheumatol 68:2575–2583. https://doi.org/10.1002/art.39759
doi: 10.1002/art.39759 pubmed: 27214788 pmcid: 5347907
Tazumi S, Yabe S, Uchiyama H (2010) Paraxial T-box genes, Tbx6 and Tbx1, are required for cranial chondrogenesis and myogenesis. Dev Biol 346:170–180. https://doi.org/10.1016/j.ydbio.2010.07.028
doi: 10.1016/j.ydbio.2010.07.028 pubmed: 20692252
Sun F, Yang Q, Weng W et al (2013) Chd4 and associated proteins function as corepressors of Sox9 expression during BMP-2-induced chondrogenesis. J Bone Miner Res 28:1950–1961. https://doi.org/10.1002/jbmr.1932
doi: 10.1002/jbmr.1932 pubmed: 23519980
Somogyi C, Matta C, Foldvari Z et al (2015) Polymodal transient receptor potential vanilloid (TRPV) ion channels in chondrogenic cells. Int J Mol Sci 16:18412–18438. https://doi.org/10.3390/ijms160818412
doi: 10.3390/ijms160818412 pubmed: 26262612
Huang M, Zhao J, Xu J et al (2019) lncRNA ADAMTS9-AS2 controls human mesenchymal stem cell chondrogenic differentiation and functions as a ceRNA. Mol Ther Nucleic Acids 18:533–545. https://doi.org/10.1016/j.omtn.2019.08.027
doi: 10.1016/j.omtn.2019.08.027 pubmed: 31671346 pmcid: 6838486
Chen K, Fang H, Xu N (2020) LncRNA LOXL1-AS1 is transcriptionally activated by JUND and contributes to osteoarthritis progression via targeting the miR-423-5p/KDM5C axis. Life Sci 258:118095. https://doi.org/10.1016/j.lfs.2020.118095
doi: 10.1016/j.lfs.2020.118095 pubmed: 32679142
Pan L, Liu D, Zhao L et al (2018) Long noncoding RNA MALAT1 alleviates lipopolysaccharide-induced inflammatory injury by upregulating microRNA-19b in murine chondrogenic ATDC5 cells. J Cell Biochem 119:10165–10175. https://doi.org/10.1002/jcb.27357
doi: 10.1002/jcb.27357 pubmed: 30145831

Auteurs

Ziji Zhang (Z)

Department of Joint Surgery, the First Affiliated Hospital of Sun Yat-Sen University, #58 zhongshan 2nd road, Guangzhou, 510080, China.

Guangxin Huang (G)

Department of Joint Surgery, The Third Affiliated Hospital of Southern Medical University, #183 zhongshan road, Guangzhou, 510630, China.

Guping Mao (G)

Department of Joint Surgery, the First Affiliated Hospital of Sun Yat-Sen University, #58 zhongshan 2nd road, Guangzhou, 510080, China. guping0913@163.com.

Shu Hu (S)

Department of Joint Surgery, The Third Affiliated Hospital of Southern Medical University, #183 zhongshan road, Guangzhou, 510630, China. hushusysu@163.com.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH