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Establishment of RT-qPCR method for telomerase catalytic subunits of mesenchymal stem cells
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Xiao-fei CHEN, Hui-ting LI, Ying-ying DONG, Yi-dan CAO, Xin-yue FU, Ming-yue LIU, Rui-rui ZHANG, Yan-hui WANG, Xin-yue WANG, Meng-shan CUI, Tong ZHANG, Lin PANG**, Chun-ming RAO**
Chinese Journal of Pharmaceutical Analysis | 2025, 45(1) : 20 - 29
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Chinese Journal of Pharmaceutical Analysis | 2025, 45(1): 20-29
Special Column for Quality Research and Evaluation of Stem Cell Products
Establishment of RT-qPCR method for telomerase catalytic subunits of mesenchymal stem cells
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Xiao-fei CHEN, Hui-ting LI, Ying-ying DONG, Yi-dan CAO, Xin-yue FU, Ming-yue LIU, Rui-rui ZHANG, Yan-hui WANG, Xin-yue WANG, Meng-shan CUI, Tong ZHANG, Lin PANG**, Chun-ming RAO**
Affiliations
  • JOINN pharmaceutical Quality Research and Testing(Beijing)Co, Ltd, Beijing 102605, China
Published: 2025-01-31 doi: 10.16155/j.0254-1793.2024-1333
Outline
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Objective:

To establish a simple and efficient method for detecting telomerase activity for evaluating tumorigenic risk of cell products.

Methods:

Specific primers and probes were designed for the conserved domain of telomerase catalytic subunit (TERT), and the primers and probes of TERT gene were optimized and screened, and the primers and probes of internal reference genes were set up. Multiple quantitative PCR reaction was performed using two-color fluorescent probes in a reaction system, and RT-qPCR probe method was established. The expression of TERT gene in human mesenchymal stem cells HMSC was used to determine whether telomerase activity existed in the cells indirectly.

Results:

TERT gene of 293T/17 positive control cells could be stably and specifically detected by this method, with a mean Ct value of 23.96 and a RSD of 1.5. The internal reference gene GAPDH could be detected successfully, the mean Ct value was 14.13, the RSD was 1.3%. The reference gene GAPDH in MRC-5 could be detected in negative control cells, the mean Ct value was 12.81, the RSD was 0.46%, the TERT gene was not detected, and the telomerase activity was negative. The reference gene GAPDH in HMSC could be detected, the Ct mean value was 13.01, and the RSD was 3.8%, whereas, the telomerase activity of HMSC was negative.

Conclusion:

The real-time fluorescent quantitative RT-qPCR probe method established in this study can accurately detect the expression of catalytic subunit mRNA in telomerase positive cells with good repeatability and high specificity. It can be used to analyze telomerase activity of stem cells and indirectly evaluate tumorigenic risk of cell products derived from stem cells.

fluorescent quantitative RT-PCR probe method  /  telomerase reverse transcriptase  /  telomerase activity  /  stem cell  /  tumorigenicity
Xiao-fei CHEN, Hui-ting LI, Ying-ying DONG, Yi-dan CAO, Xin-yue FU, Ming-yue LIU, Rui-rui ZHANG, Yan-hui WANG, Xin-yue WANG, Meng-shan CUI, Tong ZHANG, Lin PANG, Chun-ming RAO. Establishment of RT-qPCR method for telomerase catalytic subunits of mesenchymal stem cells[J]. Chinese Journal of Pharmaceutical Analysis, 2025 , 45 (1) : 20 -29 . DOI: 10.16155/j.0254-1793.2024-1333
Year 2025 volume 45 Issue 1
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Article Info
doi: 10.16155/j.0254-1793.2024-1333
  • Receive Date:2024-12-12
  • Online Date:2026-03-19
  • Published:2025-01-31
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History
  • Received:2024-12-12
Funding
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    JOINN pharmaceutical Quality Research and Testing(Beijing)Co, Ltd, Beijing 102605, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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