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Series GSE201779 Query DataSets for GSE201779
Status Public on Aug 29, 2022
Title Curcuma longa and Boswellia serrata extracts modulate different and complementary pathways on human chondrocytes in vitro: deciphering of a transcriptomic study
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Objectives: Curcuma longa (CL) and Boswellia serrata (BS) extracts are used to relieve osteoarthritis symptoms. The aim of this in vitro study was to investigate their mechanisms of action at therapeutic plasmatic concentrations on primary human osteoarthritic (OA) chondrocytes.Methods: BS (10-50 µg/mL) and CL (0.4-2 µg/mL corresponding to 1-5 µM of curcumin) were evaluated separately or in combination on primary chondrocytes isolated from 17 OA patients and cultured in alginate beads. 10 patients were used for RNA-sequencing analysis. Proteomic confirmation was performed either by immunoassays in the culture supernatant or by flow cytometry for cell surface markers after 72h of treatment. Results: Significant gene expression modifications were already observed after 6 hours of treatment at the highest dose of CL (2 µg/ml) while BS was significantly effective only after 24h of treatment whatever the concentration tested. The most over-expressed genes by CL were anti-oxidative, detoxifying, and cytoprotective genes involved in the Nrf2 pathway. Down-regulated genes were principally pro-inflammatory cytokines and chemokines. Inversely, BS anti-oxidant/detoxifying activities were related to the activation of Nrf1 and PPARα pathways. BS anti-inflammatory effects were associated with the increase of GDF15, a decrease in cholesterol cell intake and fatty acid metabolism involved genes, and a down-regulation of Toll-like receptors (TLRs) activation. As CL, BS down-regulated ADAMTS1, 5 and MMP3, 13 genes expression. The combination of both CL and BS was significantly more effective than CL or BS alone on many genes such as IL-6, CCL2, ADAMTS1, and 5. Conclusion: BS and CL have anti-oxidative, anti-inflammatory, and anti-catabolic activities suggesting a protective effect of these extracts on cartilage. Even if they share some mechanism of action, the two extracts act mainly on distinct pathways, and with different time courses, justifying their association to treat osteoarthritis.
 
Overall design RNA-Seq on primary human OA chondrocytes mRNA cultured in alginate beads in the presence or not of C. longa, B. serrata or the combination
Web link http://10.3389/fphar.2022.931914
 
Contributor(s) Sanchez C, Zappia J, Lambert C, Foguenne J, Dierckxsens Y, Dubuc J, Delcour J, Gothot A, Henrotin Y
Citation(s) 36034822
Submission date Apr 28, 2022
Last update date Aug 30, 2022
Contact name Christelle Sanchez
E-mail(s) christelle.sanchez@uliege.be
Organization name ULiege
Lab dBRU
Street address Quai G. Kurth 45
City Liège
ZIP/Postal code 4020
Country Belgium
 
Platforms (1)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
Samples (140)
GSM6071216 CR16 6h CTRL
GSM6071217 CR16 6h CL1
GSM6071218 CR16 6h CL2
Relations
BioProject PRJNA833031

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE201779_merged_gene_counts.txt.gz 5.3 Mb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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