Botigelli, Ramon Cesar [UNESP]Pieri, Naira Carolina GodoyBessi, Brendon WilliamMachado, Lucas SimõesBridi, Alessandrade Souza, Aline FernandaRecchia, KaianaNeto, Paulo FantinatoRoss, Pablo JuanBressan, Fabiana FernandesNogueira, Marcelo Fábio Gouveia [UNESP]2023-07-292023-07-292022-09-14Frontiers in Cell and Developmental Biology, v. 10.2296-634Xhttp://hdl.handle.net/11449/247683Several opportunities for embryo development, stem cell maintenance, cell fate, and differentiation have emerged using induced pluripotent stem cells (iPSCs). However, the difficulty in comparing bovine iPSCs (biPSCs) with embryonic stem cells (ESCs) was a challenge for many years. Here, we reprogrammed fetal fibroblasts by transient expression of the four transcription factors (Oct4, Sox2, Klf4, and c-Myc, collectively termed “OSKM” factors) and cultured in iPSC medium, supplemented with bFGF, bFGF2i, leukemia inhibitory factor (LIF), or LIF2i, and then compared these biPSC lines with bESC to evaluate the pluripotent state. biPSC lines were generated in all experimental groups. Particularly, reprogrammed cells treated with bFGF were more efficient in promoting the acquisition of pluripotency. However, LIF2i treatment did not promote continuous self-renewal. biPSCs (line 2) labeled with GFP were injected into early embryos (day 4.5) to assess the potential to contribute to chimeric blastocysts. The biPSC lines show a pluripotency state and are differentiated into three embryonic layers. Moreover, biPSCs and bESCs labeled with GFP were able to contribute to chimeric blastocysts. Additionally, biPSCs have shown promising potential for contributing to chimeric blastocysts and for future studies.engbovinecellular reprogrammingembryonic stem cellsinduced pluripotent stem cellspluripotency maintenanceArtigo10.3389/fcell.2022.9387092-s2.0-85138967942