期刊
FEBS JOURNAL
卷 288, 期 14, 页码 4394-4411出版社
WILEY
DOI: 10.1111/febs.15744
关键词
bovine EPSCs; bovine iPSCs; bovine– mouse chimeras; LCDM medium
资金
- Major Projects of Natural Science Foundation of InnerMongolia Autonomous Region [2020ZD10]
- Science and Technology Major Project of the Inner Mongolia Autonomous Region of China [2020ZD0007, zdzx2018065]
- Natural Science Foundation of Inner Mongolia Autonomous Region [2020BS03003, 2020BS03022]
- Research Foundation for Advanced Talents of Inner Mongolia University [30500-5185138, 30500-5205160]
- National Transgenic Project of China [2016ZX08010001-002]
- National Natural Science Foundation of China [31460309]
- Undergraduate Innovation and Entrepreneurship Training Program [201914362]
This study successfully derived bovine extended pluripotent stem cells (EPSCs) using the LCDM medium, showing their ability to contribute to embryonic and extraembryonic tissues in pre-implantation blastocysts and postimplantation bovine-mouse chimeras. Transcriptome analysis revealed the unique molecular characteristics of bovine EPSCs compared with induced pluripotent stem cells (iPSCs), providing a foundation for further research in biology, medicine, and agriculture.
Cattle have emerged as one of the most important domestic animals widely used for meat, milk, and fur. Derivation of bovine pluripotent stem cells (PSCs) can be applied in drug selecting and human disease modeling and facilitated agriculture-related applications such as production of genetically excellent cattle by gene editing. Extended PSCs (EPSCs), capable of differentiating into embryonic and extraembryonic parts, have been generated in mouse, human, and pig. Whether bovine EPSCs could be generated, and their chimeric competency remains unclear. This study focused on derivation of bovine EPSCs using LCDM medium and exploring the characteristics of EPSCs among different species, including bovine, mouse, and human EPSCs. Here, using LCDM medium (consisting of hLIF, CHIR99021, (S)-(+)-dimethindene maleate, and minocycline hydrochloride) enables the derivation of bovine EPSCs from induced PSCs (iPSCs) and bovine fetal fibroblasts (BFF) with stable morphology, pluripotent marker expression, and in vitro differentiation ability. Notably, bovine EPSCs exhibited interspecies chimeric contribution to embryonic and extraembryonic tissues in pre-implantation blastocysts and postimplantation bovine-mouse chimeras. Transcriptome analysis revealed the unique molecular characteristics of bovine EPSCs compared with iPSCs. The similarities and differences in molecular features across bovine, human, and mouse EPSCs were also described by transcriptome analysis. Taken together, the LCDM culture system containing chemical cocktails can be used for the establishment and long-term passaging of bovine EPSCs with embryonic and extraembryonic potency in bovine-mouse chimeras. Our findings lay the foundation of generating PSCs in domestic animals and open avenues for basic and applied research in biology, medicine, and agriculture. Database Gene expression data of bovine EPSCs and bovine iPSCs are available in the GEO databases under the accession number PRJNA693452.
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