Wang, D.; Ming, H.; Yang, D.; Tsai, L.-K.; Wei, Z.; Scatolin, G. N.; Wang, X.; Yau, K.; Tao, L.; Tong, X.; Wang, S.; Shi, K.-X.; Evseenko, D.; Handel, B. V.; Zhang, B.; Wang, Y.; Iyyappan, R.; Ojeda-Rojas, O. A.; Hu, G.; McGinnis, L.; Paulson, R.; Mckim, D.; Kong, X.; Xia, X.; Zhang, J.; Chen, E. Y.; Xu, J.; Jiang, Z.; Ying, Q.-L.

The derivation of authentic embryonic stem cells (ESCs) from diverse mammalian species offers valuable opportunities for advancing regenerative medicine, studying developmental biology, and enabling species conservation. Here, we report the development of a robust, serum-free culture system, termed 6iL/E4 that enables the derivation and long-term self-renewal of ESCs from multiple mammalian species, including mouse, rat, bovine, rabbit, and human. Using systematic signaling pathway analysis, we identified key regulators--including GSK3, STAT3, PDGFR, BRAF, and LATS--critical for ESC maintenance across species. Additionally, inducible expression of KLF2 and NANOG enhances the naive pluripotency and chimeric potential of bovine ESCs. The E4 medium also supports stable ESC growth while minimizing lineage bias. These findings reveal conserved principles underlying ESC self-renewal across divergent mammalian species and provide a universal platform for cross-species stem cell research, disease modeling, and biotechnology applications.