Identification of Mesenchymal Stem Cell Gene Markers for Quality Control

keywords_en.jpgMesenchymal Stem Cell, Biomarker, Serum Free Culture Medium 

division_en.jpg Graduate School of Advanced Sciences of Matter Department of Molecular Biotechnology

position_en.jpgAssociate Professor



We have been developing Bone Marrow Stem cell (BM-MSC)
and Synovial MSC (SY-MSC) culture systems to transplant for
clinical osteo/chondrocytes regeneration by using serum free
culture medium, STK. The STK medium is chemically defined
and the MSCs were more proliferative under the STK, so that
we aim to confirm the system is safe and highly efficient for
clinical use.

Research Summary

In order to develop the serum free cultured MSC system, we
need to set up biomarkers of cultured MSCs for quality control.
We have already examined gene expression profiles of BMMSCs
cultured in serum containing medium and screened the
candidate gene markers by examining their gene expression
levels of more than 40 human BM-MSC lines. In this on going
project, we are searching for candidate gene markers of SYMSCs
in the following 2 steps.
Step 1) Set up gene markers of SY-MSC cultured in serum
containing medium. A) By examining mRNA expression of gene markers set up in the BM-MSCs cultured in serum
containing medium. B) By analyzing gene expression profiles using DNA microarray technique.
Step 2) Set up gene markers of SY-MSC cultured in STK medium by the methods shown above.


We picked up several of candidate gene markers from SY-MSCs cultured in serum containing medium. We prepared
test samples of BM-MSCs, SY-MSCs, and Fibroblasts to test the candidate marker gene expression. Availability of the
serum medium cultured BM-MSC markers in SY-MSCs is still tested. We are also collecting additional test SY-MSC
samples from donated synovial tissues for future examination.

For Application

Tissue regeneration therapy.

Competitive Advances

Quality of MSCs were examined by detecting combination of cell surface antigens of MSCs using flowcytometry
technique conventionally. However, this methods needs many numbers of MSCs to judge the cell quality. Our strategy
has advantages in the following points,
1) We just need less number of the cells for quality control. 2) we can set up the gene markers that ensure the SYMSC
quality based on characteristics of the MSCs, such as undifferentiated status/stemness, non contamination of
other cell source, non malignancy, etc.


Kato, Y., et., al. Hiroshima Shi-shi, 39, p1~p8, 2011.