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Updated: Jan 15, 2026

Alternative Cultures for Human Pluripotent Stem Cell Production, Maintenance, and Genetic Analysis
Published on: July 24, 2014
NN15-017 promotes human pluripotent stem cell proliferation and generation
Shizuka Fujigaki-Yamazaki1, Ryoko Nakatani1, Osamu Hirata2
1Division of Clinical Basis for ES Cell Research, Center for Human ES Cell Research, Institute for Life and Medical Sciences, Kyoto University, 53 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.
A new compound, NN15-017, significantly reduces the need for FGF2 in culturing human pluripotent stem cells (hPSCs). This discovery enhances induced PSC generation and offers benefits for hPSC proliferation.
Area of Science:
- Stem Cell Biology
- Cell Culture Optimization
- Biotechnology
Background:
- Human pluripotent stem cells (hPSCs) require specific nutrients for culture, often including FGF2.
- FGF2 is critical for hPSC growth and maintenance, but alternatives are sought for defined media.
Purpose of the Study:
- To identify compounds that can substitute for FGF2 activity in hPSC culture.
- To find compounds that promote proliferation and reprogramming efficiency of hPSCs.
Main Methods:
- Screened a compound library using an hOCT4-EGFP reporter system.
- Evaluated candidate compounds via morphology, OCT4 immunostaining, and long-term culture.
- Assessed reprogramming efficiency and analyzed activated signaling pathways.
Main Results:
- Identified NN15-017, a compound that allows a 5-fold reduction in FGF2 concentration.
- NN15-017 enhanced human induced PSC reprogramming efficiency by 2- to 3-fold.
- NN15-017 activated MAP/ERK signaling and potentially affected Hippo-YAP signaling.
Conclusions:
- NN15-017 reduces FGF2 requirements for hPSC culture.
- This compound offers benefits for hPSC proliferation and the generation of induced PSCs.
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