NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE241333 Query DataSets for GSE241333
Status Public on Sep 20, 2023
Title Real-time quantitative PCR analysis of microRNAs in a mice model of Neurogenic Heterotopic Ossifications (NHOs)
Platform organisms Mus musculus; Rattus norvegicus
Sample organism Mus musculus
Experiment type Other
Summary Neurogenic heterotopic ossifications are intramuscular bone formations developing following central nervous system injury. The pathophysiology is poorly understood and current treatments for this debilitating condition remain unsatisfying. Here we explored the role of miRNAs in a clinically relevant mouse model that combines muscle and spinal cord injury (SCI), and in patients’ cells. We found an osteo-suppressive miRNAs response in injured muscle that was hindered when the spinal cord injury was associated. In isolated fibro-adipogenic progenitors from damaged muscle (cells at the origin of ossification), spinal cord injury induced a downregulation of osteo-suppressive miRNAs while osteogenic markers were overexpressed. The overexpression of selected miRNAs in patient’s fibro-adipogenic progenitors inhibited mineralization and osteo-chondrogenic markers in vitro. Altogether, we highlighted an osteo-suppressive mechanism involving multiple miRNAs in response to muscle injury that prevents osteogenic commitment and which is ablated by the neurologic lesion in heterotopic ossification pathogenesis. This provides new research hypotheses for preventive treatments.
 
Overall design These data were generated from RT-qPCR miRNA arrays on pooled samples (n=3 independant biological replicates) from control (SHAM+PBS), damaged (SHAM+CDTX), spinalized (SCI+PBS) or NHOs developping (SCI+CDTX) muscles from mice gastrocnemius biopsy at 2 or 4 days after induction. MicroRNAs screening was performed using miRNome Mouse&Rat panel I+II (V5, 339322, Qiagen). These results were subsequently validated in RT-qPCR for each individual donor (n=6 independant biological replicates) in the linked manuscript.
 
Contributor(s) Gueguen J, Girard D, Rival B, Fernandez J, Goriot M, Banzet S
Citation(s) 37700159
Submission date Aug 21, 2023
Last update date Sep 20, 2023
Contact name Jules GUEGUEN
E-mail(s) julesgueguen1995@gmail.com
Organization name French Armed Forces Biomedical Research Institute (IRBA)
Street address 1 Rue Lieutenant Raoul Batany
City Clamart
ZIP/Postal code 92140
Country France
 
Platforms (1)
GPL33702 Qiagen miRNome Mouse&Rat panel I+II
Samples (8)
GSM7725846 SHAM surgery, PBS injection, D2
GSM7725847 SHAM surgery, CDTX injection, D2
GSM7725848 SCI surgery, PBS injection, D2
Relations
BioProject PRJNA1007697

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
GSE241333_Results.xlsx 140.7 Kb (ftp)(http) XLSX
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap