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Elucidation of the pluripotent potential of bovine embryonic lineages facilitates the establishment of formative stem cell lines

  • Minglei Zhi,
  • Dengfeng Gao,
  • Yixuan Yao,
  • Zimo Zhao,
  • Yingjie Wang,
  • Pengcheng He,
  • Zhiqiang Feng,
  • Jinying Zhang,
  • Ziqi Huang,
  • Wenyuan Gu,
  • Jianglin Zhao,
  • He Zhang,
  • Shunxin Wang,
  • Xin Li,
  • Qiang Zhang,
  • Zengyuan Zhao,
  • Xinze Chen,
  • Xiaowei Zhang,
  • Lun Qin,
  • Jun Liu,
  • Chengjun Liu,
  • Suying Cao,
  • Shuai Gao,
  • Wenli Yu,
  • Zhu Ma,
  • Jianyong Han

摘要

The establishment of epiblast-derived pluripotent stem cells (PSCs) from cattle, which are important domestic animals that provide humans with milk and meat while also serving as bioreactors for producing valuable proteins, poses a challenge due to the unclear molecular signaling required for embryonic epiblast development and maintenance of PSC self-renewal. Here, we selected six key stages of bovine embryo development (E5, E6, E7, E10, E12, and E14) to track changes in pluripotency and the dependence on signaling pathways via modified single-cell transcription sequencing technology. The remarkable similarity of the gene expression patterns between cattle and pigs during embryonic lineage development contributed to the successful establishment of bovine epiblast stem cells (bEpiSCs) using 3i/LAF (WNTi, GSK3βi, SRCi, LIF, Activin A, and FGF2) culture system. The generated bEpiSCs exhibited consistent expression patterns of formative epiblast pluripotency genes and maintained clonal morphology, normal karyotypes, and proliferative capacity for more than 112 passages. Moreover, these cells exhibited high-efficiency teratoma formation as well as the ability to differentiate into various cell lineages. The potential of bEpiSCs for myogenic differentiation, primordial germ cell like cells (PGCLCs) induction, and as donor cells for cell nuclear transfer was also assessed, indicating their promise in advancing cell-cultured meat production, gene editing, and animal breeding.