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牛胚胎外内胚层细胞的建立。

Establishment of bovine extraembryonic endoderm cells.

作者信息

Ming Hao, Scatolin Giovanna N, Ojeda Alejandro, Jiang Zongliang

机构信息

Department of Animal Sciences, Genetics Institute, University of Florida, Gainesville, FL 32610, USA.

Department of Large Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610, USA.

出版信息

bioRxiv. 2024 Dec 17:2024.12.17.628911. doi: 10.1101/2024.12.17.628911.

Abstract

Understanding the mechanisms of hypoblast development and its role in the implantation is critical for improving farm animal reproduction, but it is hampered by the lack of research models. Here we report that a chemical cocktail (FGF4, BMP4, IL-6, XAV939, and A83-01) enables de novo derivation and long-term culture of bovine extraembryonic endoderm cells (bXENs). Transcriptomic and epigenomic analyses confirmed the identity of bXENs and revealed that they are resemble hypoblast lineages of early bovine peri-implantation embryos. We showed that bXENs help maintain the stemness of bovine ESCs and prevent them from differentiation. In the presence of a signaling cocktail sustaining bXENs, the growth and progression of epiblasts are also facilitated in the developing pre-implantation embryo. Furthermore, through 3D assembly of bXENs with bovine ESCs and TSCs, we developed an improved bovine blastocyst like structure (bovine blastoid) that resembles blastocyst. The bovine XENs and blastoids established in this study represent accessible models for understanding hypoblast development and improving reproductive efficiency in livestock species.

摘要

了解下胚层发育机制及其在着床中的作用对于提高家畜繁殖能力至关重要,但由于缺乏研究模型而受到阻碍。在此,我们报告一种化学混合物(FGF4、BMP4、IL-6、XAV939和A83-01)能够实现牛胚外内胚层细胞(bXENs)的从头衍生和长期培养。转录组学和表观基因组学分析证实了bXENs的特性,并表明它们类似于早期牛着床周围胚胎的下胚层谱系。我们发现bXENs有助于维持牛胚胎干细胞的干性并防止其分化。在存在维持bXENs的信号混合物的情况下,着床前发育胚胎中胚泡的生长和发育也得到促进。此外,通过将bXENs与牛胚胎干细胞和滋养层干细胞进行3D组装,我们构建了一种改进的类似牛囊胚的结构(牛胚状体)。本研究中建立的牛XENs和胚状体为理解下胚层发育和提高家畜繁殖效率提供了可及的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e29f/11702706/fa66c51f2118/nihpp-2024.12.17.628911v1-f0001.jpg

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