Department of Biological Sciences, California State University Chico, Chico, CA, United States of America.
Department of Computer Sciences, California State University Chico, Chico, CA, United States of America.
PLoS One. 2018 May 14;13(5):e0196872. doi: 10.1371/journal.pone.0196872. eCollection 2018.
Hematopoiesis is an essential and highly regulated biological process that begins with hematopoietic stem cells (HSCs). In healthy organisms, HSCs are responsible for generating a multitude of mature blood cells every day, yet the molecular pathways that instruct HSCs to self-renew and differentiate into post-mitotic blood cells are not fully known. To understand these molecular pathways, we investigated novel genes expressed in hematopoietic-supportive cell lines from the zebrafish (Danio rerio), a model system increasingly utilized to uncover molecular pathways important in the development of other vertebrate species. We performed RNA sequencing of the transcriptome of three stromal cell lines derived from different stages of embryonic and adult zebrafish and identified hundreds of highly expressed transcripts. For our studies, we focused on isthmin 1 (ism1) due to its shared synteny with its human gene ortholog and because it is a secreted protein. To characterize ism1, we performed loss-of-function experiments to identify if mature blood cell production was disrupted. Myeloid and erythroid lineages were visualized and scored with transgenic zebrafish expressing lineage-specific markers. ism1 knockdown led to reduced numbers of neutrophils, macrophages, and erythrocytes. Analysis of clonal methylcellulose assays from ism1 morphants also showed a reduction in total hematopoietic stem and progenitor cells (HSPCs). Overall, we demonstrate that ism1 is required for normal generation of HSPCs and their downstream progeny during zebrafish hematopoiesis. Further investigation into ism1 and its importance in hematopoiesis may elucidate evolutionarily conserved processes in blood formation that can be further investigated for potential clinical utility.
造血是一个重要且高度受调控的生物学过程,起始于造血干细胞(HSCs)。在健康的生物体中,HSCs 每天负责生成大量成熟的血细胞,然而,指导 HSCs 自我更新并分化为有丝分裂后血细胞的分子途径尚不完全清楚。为了理解这些分子途径,我们研究了来自斑马鱼(Danio rerio)造血支持细胞系中表达的新基因,斑马鱼是一个越来越多地用于揭示其他脊椎动物物种发育中重要分子途径的模型系统。我们对来自胚胎和成年斑马鱼不同阶段的三种基质细胞系的转录组进行了 RNA 测序,鉴定了数百个高表达的转录本。在我们的研究中,我们专注于伊斯坦敏 1(ism1),因为它与人类基因直系同源物具有共同的基因序列,并且它是一种分泌蛋白。为了表征 ism1,我们进行了功能丧失实验,以确定是否破坏了成熟血细胞的产生。我们用表达谱系特异性标记的转基因斑马鱼可视化和评分髓系和红细胞谱系。ism1 敲低导致中性粒细胞、巨噬细胞和红细胞数量减少。从 ism1 突变体的克隆甲基纤维素测定分析也显示总造血干细胞和祖细胞(HSPCs)减少。总的来说,我们证明 ism1 是斑马鱼造血过程中正常产生 HSPCs 及其下游祖细胞所必需的。对 ism1 及其在造血中的重要性的进一步研究可能阐明血液形成中保守的进化过程,这些过程可以进一步研究其潜在的临床应用。