| Literature DB >> 33615198 |
Shota Someya1, Shugo Tohyama1,2, Kotaro Kameda1, Sho Tanosaki1, Yuika Morita1, Kazunori Sasaki3, Moon-Il Kang3, Yoshikazu Kishino1, Marina Okada1, Hidenori Tani1, Yusuke Soma1, Kazuaki Nakajima1, Tomohiko Umei1, Otoya Sekine1, Taijun Moriwaki1, Hideaki Kanazawa1, Eiji Kobayashi2, Jun Fujita1,4, Keiichi Fukuda1.
Abstract
Human pluripotent stem cells (hPSCs) have a unique metabolic signature for maintenance of pluripotency, self-renewal, and survival. Although hPSCs could be potentially used in regenerative medicine, the prohibitive cost associated with large-scale cell culture presents a major barrier to the clinical application of hPSC. Moreover, without a fully characterized metabolic signature, hPSC culture conditions are not optimized. Here, we performed detailed amino acid profiling and found that tryptophan (TRP) plays a key role in the proliferation with maintenance of pluripotency. In addition, metabolome analyses revealed that intra- and extracellular kynurenine (KYN) is decreased under TRP-supplemented conditions, whereas N-formylkynurenine (NFK), the upstream metabolite of KYN, is increased thereby contributing to proliferation promotion. Taken together, we demonstrate that TRP is indispensable for survival and proliferation of hPSCs. A deeper understanding of TRP metabolism will enable cost-effective large-scale production of hPSCs, leading to advances in regenerative medicine.Entities:
Keywords: Cell Biology; Metabolomics; Stem Cell Research
Year: 2021 PMID: 33615198 PMCID: PMC7878994 DOI: 10.1016/j.isci.2021.102090
Source DB: PubMed Journal: iScience ISSN: 2589-0042