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Article

Identification of optimal reference genes for quantitative PCR studies on human mesenchymal stem cells

  • Authors:
    • Xiuying Li
    • Qiwei Yang
    • Jinping Bai
    • Yanyan Yang
    • Lingzhi Zhong
    • Yimin Wang
  • View Affiliations / Copyright

    Affiliations: The Central Laboratory, China-Japan Union Hospital, Jilin University, Changchun, Jilin 130033, P.R. China, Department of Pathology, Jilin University, The Key Laboratory of Pathobiology, Ministry of Education, Changchun, Jilin 130021, P.R. China
  • Pages: 1304-1311
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    Published online on: November 3, 2014
       https://doi.org/10.3892/mmr.2014.2841
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Abstract

Quantitative polymerase chain reaction (qPCR) analysis is a commonly used method for the study of mRNA expression throughout the field of mesenchymal stem cell (MSC) research. This technology is simple and sensitive; however the results may vary significantly due to the use of various reference genes (RGs) as normalizers. Therefore, the reliable use of RGs is vital for obtaining accurate results. The present study focuses on ten putative RGs for the normalization of qPCR data between human bone marrow-derived MSCs (BM-MSCs) and fetal tissue-derived MSCs (FT-MSCs). The total RNA from these two types of MSC was isolated using TRIzol reagent. cDNA was generated from the RNA via reverse transcription and subsequently analyzed by qPCR using ten common RGs as normalizers. These RGs included 18S, ACTB, B2M, HPRT1, GAPDH, TBP, PPIA, RPLP0, PGK1 and RPL13A. GeNorm, NormFinder and BestKeeper software were used to analyze the qPCR results by evaluating the expression stabilities of the ten candidate RGs in BM-MSCs and FT-MSCs. Consequently, several of the commonly used RGs, including 18S, ACTB and TBP, were demonstrated to be unsuitable for normalization in these two MSCs, whereas RPL13A, B2M and PPIA were the most stable RGs and were therefore reliable for use in qPCR studies. Combining multiple RGs had no contribution towards increasing their stabilities. In conclusion, the present study revealed that RPL13A, B2M and PPIA were the optimal RGs for qPCR studies comparing BM-MSCs and FT-MSCs.
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Copy and paste a formatted citation
Spandidos Publications style
Li X, Yang Q, Bai J, Yang Y, Zhong L and Wang Y: Identification of optimal reference genes for quantitative PCR studies on human mesenchymal stem cells. Mol Med Rep 11: 1304-1311, 2015.
APA
Li, X., Yang, Q., Bai, J., Yang, Y., Zhong, L., & Wang, Y. (2015). Identification of optimal reference genes for quantitative PCR studies on human mesenchymal stem cells. Molecular Medicine Reports, 11, 1304-1311. https://doi.org/10.3892/mmr.2014.2841
MLA
Li, X., Yang, Q., Bai, J., Yang, Y., Zhong, L., Wang, Y."Identification of optimal reference genes for quantitative PCR studies on human mesenchymal stem cells". Molecular Medicine Reports 11.2 (2015): 1304-1311.
Chicago
Li, X., Yang, Q., Bai, J., Yang, Y., Zhong, L., Wang, Y."Identification of optimal reference genes for quantitative PCR studies on human mesenchymal stem cells". Molecular Medicine Reports 11, no. 2 (2015): 1304-1311. https://doi.org/10.3892/mmr.2014.2841
Copy and paste a formatted citation
x
Spandidos Publications style
Li X, Yang Q, Bai J, Yang Y, Zhong L and Wang Y: Identification of optimal reference genes for quantitative PCR studies on human mesenchymal stem cells. Mol Med Rep 11: 1304-1311, 2015.
APA
Li, X., Yang, Q., Bai, J., Yang, Y., Zhong, L., & Wang, Y. (2015). Identification of optimal reference genes for quantitative PCR studies on human mesenchymal stem cells. Molecular Medicine Reports, 11, 1304-1311. https://doi.org/10.3892/mmr.2014.2841
MLA
Li, X., Yang, Q., Bai, J., Yang, Y., Zhong, L., Wang, Y."Identification of optimal reference genes for quantitative PCR studies on human mesenchymal stem cells". Molecular Medicine Reports 11.2 (2015): 1304-1311.
Chicago
Li, X., Yang, Q., Bai, J., Yang, Y., Zhong, L., Wang, Y."Identification of optimal reference genes for quantitative PCR studies on human mesenchymal stem cells". Molecular Medicine Reports 11, no. 2 (2015): 1304-1311. https://doi.org/10.3892/mmr.2014.2841
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