Department of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Department of Developmental Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Methods Mol Biol. 2025;2848:85-103. doi: 10.1007/978-1-0716-4087-6_6.
Recent technological advances in single-cell RNA sequencing (scRNA-Seq) have enabled scientists to answer novel questions in biology with unparalleled precision. Indeed, in the field of ocular development and regeneration, scRNA-Seq studies have resulted in a number of exciting discoveries that have begun to revolutionize the way we think about these processes. Despite the widespread success of scRNA-Seq, many scientists are wary to perform scRNA-Seq experiments due to the uncertainty of obtaining high-quality viable cell populations that are necessary for the generation of usable data that enable rigorous computational analyses. Here, we describe methodology to reproducibility generate high-quality single-cell suspensions from embryonic zebrafish eyes. These single-cell suspensions served as inputs to the 10× Genomics v3.1 system and yielded high-quality scRNA-Seq data in proof-of-principle studies. In describing methodology to quantitatively assess cell yields, cell viability, and other critical quality control parameters, this protocol can serve as a useful starting point for others in designing their scRNA-Seq experiments in the zebrafish eye and in other developing or regenerating tissues in zebrafish or other model systems.
单细胞 RNA 测序(scRNA-Seq)的最新技术进步使科学家能够以前所未有的精度回答生物学中的新问题。事实上,在眼部发育和再生领域,scRNA-Seq 研究已经取得了一些令人兴奋的发现,这些发现开始改变我们对这些过程的看法。尽管 scRNA-Seq 取得了广泛的成功,但由于获得高质量的可行细胞群体的不确定性,许多科学家对进行 scRNA-Seq 实验持谨慎态度,这些群体是生成可用于严格计算分析的可用数据所必需的。在这里,我们描述了一种可重现地从胚胎斑马鱼眼睛中生成高质量单细胞悬液的方法。这些单细胞悬液作为 10× Genomics v3.1 系统的输入,并在原理验证研究中产生了高质量的 scRNA-Seq 数据。在描述定量评估细胞产量、细胞活力和其他关键质量控制参数的方法时,本方案可以为其他在斑马鱼眼睛或其他发育或再生组织中设计 scRNA-Seq 实验的人提供有用的起点,也可以为其他斑马鱼或其他模型系统中的组织提供起点。