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单细胞 RNA 测序分析揭示猴多能干细胞向原始生殖样细胞分化的发育轨迹†。

Mapping developmental paths of monkey primordial germ-like cells differentiation from pluripotent stem cells by single cell ribonucleic acid sequencing analysis†.

机构信息

Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology and Key Laboratory of Assisted Reproduction, Ministry of Education, Peking University Third Hospital, Beijing, China.

College of Veterinary Medicine, South China Agricultural University, Guangzhou, China.

出版信息

Biol Reprod. 2022 Jul 25;107(1):237-249. doi: 10.1093/biolre/ioac133.

Abstract

The induction of primordial germ-like cells (PGCLCs) from pluripotent stem cells (PSCs) provides a powerful system to study the cellular and molecular mechanisms underlying germline specification, which are difficult to study in vivo. The studies reveal the existence of a species-specific mechanism underlying PGCLCs between humans and mice, highlighting the necessity to study regulatory networks in more species, especially in primates. Harnessing the power of single-cell RNA sequencing (scRNA-seq) analysis, the detailed trajectory of human PGCLCs specification in vitro has been achieved. However, the study of nonhuman primates is still needed. Here, we applied an embryoid body (EB) differentiation system to induce PGCLCs specification from cynomolgus monkey male and female PSCs, and then performed high throughput scRNA-seq analysis of approximately 40 000 PSCs and cells within EBs. We found that EBs provided a niche for PGCLCs differentiation by secreting growth factors critical for PGCLC specification, such as bone morphogenetic protein 2 (BMP2), BMP4, and Wnt Family Member 3. Moreover, the developmental trajectory of PGCLCs was reconstituted, and gene expression dynamics were revealed. Our study outlines the roadmap of PGCLC specification from PSCs and provides insights that will improve the differentiation efficiency of PGCLCs from PSCs.

摘要

多能干细胞(PSCs)中原始生殖细胞样细胞(PGCLCs)的诱导为研究生殖细胞特化的细胞和分子机制提供了一个强大的系统,而这些机制在体内很难研究。这些研究揭示了人类和小鼠之间 PGCLCs 之间存在特定于物种的机制,强调了有必要在更多物种,特别是灵长类动物中研究调控网络。利用单细胞 RNA 测序(scRNA-seq)分析的力量,已经实现了体外人类 PGCLCs 特化的详细轨迹。然而,仍需要研究非人类灵长类动物。在这里,我们应用胚状体(EB)分化系统从食蟹猴雄性和雌性 PSCs 中诱导 PGCLCs 特化,然后对大约 40,000 个 PSCs 和 EBs 内的细胞进行高通量 scRNA-seq 分析。我们发现,EB 通过分泌对 PGCLC 特化至关重要的生长因子,如骨形态发生蛋白 2(BMP2)、BMP4 和 Wnt 家族成员 3,为 PGCLC 分化提供了一个小生境。此外,还重建了 PGCLCs 的发育轨迹,并揭示了基因表达动力学。我们的研究概述了从 PSCs 中特化 PGCLCs 的路线图,并提供了将提高从 PSCs 中分化 PGCLCs 的效率的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1771/9310512/c8a8cd2f88c8/ioac133ga.jpg

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