Doxycycline supplementation allows for the culture of human ESCs/iPSCs with media changes at 3-day intervals
- Stem Cell Res. 2015 Nov;15(3):608-613. doi: 10.1016/j.scr.2015.10.007.
- 1. Department of Biochemistry and Molecular Biology, College of Medicine, Hanyang University, Republic of Korea; Hanyang Biomedical Research Institute, Hanyang University, Republic of Korea.
- 2. Hanyang Biomedical Research Institute, Hanyang University, Republic of Korea; Graduate School of Biomedical Science and Engineering, Hanyang University, Republic of Korea.
- 3. Department of Biochemistry and Molecular Biology, College of Medicine, Hanyang University, Republic of Korea; Hanyang Biomedical Research Institute, Hanyang University, Republic of Korea; Graduate School of Biomedical Science and Engineering, Hanyang University, Republic of Korea. Electronic address: [email protected].
Culturing human embryonic stem and induced pluripotent stem cells (hESCs/iPSCs) is one of the most costly and labor-intensive tissue cultures, as media containing expensive factors/cytokines should be changed every day to maintain and propagate undifferentiated hESCs/iPSCs in vitro. We recently reported that doxycycline, an anti-bacterial agent, had dramatic effects on hESC/iPSC survival and promoted self-renewal. In this study, we extended the effects of doxycycline to a more practical issue to save cost and labor in hESC/iPSC cultures. Regardless of cultured cell conditions, hESCs/iPSCs in doxycycline-supplemented media were viable and proliferating for at least 3 days without media change, while none or few viable cells were detected in the absence of doxycycline in the same conditions. Thus, hESCs/iPSCs supplemented with doxycycline can be cultured for a long period of time with media changes at 3-day intervals without altering their self-renewal and pluripotent properties, indicating that doxycycline supplementation can reduce the frequency of media changes and the amount of media required by 1/3. These findings strongly encourage the use of doxycycline to save cost and labor in culturing hESCs/iPSCs.
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