Canine Adipose Derived Mesenchymal Stem Cells Transcriptome Composition Alterations: A Step towards Standardizing Therapeutic.
Nina KrešićIvana ŠimićIvana LojkićTomislav BedekovićPublished in: Stem cells international (2017)
Although canine adipose derived stem cells (cASCs) morphology characteristics and differentiation ability are well documented, transcriptome alterations of undifferentiated cASCs during ex vivo cultivation remain unknown. Here we demonstrate, for the first time, the transcriptome composition of isolated cASCs in undifferentiated state originating from six donors. Transcriptome changes were monitored during ex vivo cultivation between passage 3 (P3) and P5, which are mostly used in therapy. Influence of donors' age in given passage number on transcriptome composition was also investigated. Cultivation from P3 to P5 resulted in 16 differentially expressed genes with cooverexpression of pluripotency and self-renewal transcription factors genes SOX2 and POU5F1 dominant in old donors' cells. Furthermore, cASCs demonstrated upregulation of IL-6 in young and old donors' cells. In addition, ex vivo cultivation of cASCs revealed well-known morphological alterations accompanied with decrease in expression of CD90 and CD44 markers in P4 and higher monitored by flow cytometry and successful osteo- and chondrodifferentiation but inefficient adipodifferentiation in P3. Our results revealed the impact of ex vivo cultivation on nature of cells. Correlation of transcriptome changes with secretome composition is needed and its further impact on therapeutic potential of cASCs remains to be evaluated in clinical trials.
Keyphrases
- single cell
- genome wide
- rna seq
- induced apoptosis
- gene expression
- cell cycle arrest
- clinical trial
- mesenchymal stem cells
- transcription factor
- flow cytometry
- poor prognosis
- dna methylation
- stem cells
- signaling pathway
- endoplasmic reticulum stress
- cell death
- oxidative stress
- randomized controlled trial
- kidney transplantation
- cell proliferation
- high resolution
- cell therapy
- genome wide identification
- long non coding rna
- double blind
- dna binding