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骨成型蛋白抑制剂 M 和 Kit 配体在斑马鱼胚胎发生过程中控制造血干细胞命运。

Oncostatin M and Kit-Ligand Control Hematopoietic Stem Cell Fate during Zebrafish Embryogenesis.

机构信息

University of Geneva, Faculty of Medicine, Department of Pathology and Immunology, CMU, University of Geneva, 1 Rue Michel-Servet, Geneva 1211, Switzerland.

University of Geneva, Faculty of Medicine, Department of Pathology and Immunology, CMU, University of Geneva, 1 Rue Michel-Servet, Geneva 1211, Switzerland.

出版信息

Stem Cell Reports. 2018 Jun 5;10(6):1920-1934. doi: 10.1016/j.stemcr.2018.04.016. Epub 2018 May 17.

Abstract

Understanding the molecular pathways controlling hematopoietic stem cell specification and expansion is a necessary milestone to perform regenerative medicine. Here, we used the zebrafish model to study the role of the ckit signaling pathway in this process. We show the importance of kitb/kitlgb signaling in the specification and expansion of hematopoietic stem cells (HSCs), in the hemogenic endothelium and caudal hematopoietic tissue (CHT), respectively. Moreover, we identified the zebrafish ortholog of Oncostatin M (osm) in the zebrafish genome. We show that the osm/osmr pathway acts upstream of kitb during specification of the hemogenic endothelium, while both pathways act synergistically to expand HSCs in the CHT. Moreover, we found that osm, in addition to its role in promoting HSC proliferation, inhibits HSC commitment to the lymphoid fate. Altogether, our data identified two cytokines, kitlgb and osm, secreted by the vascular niche, that control HSCs during early embryonic development.

摘要

了解控制造血干细胞特化和扩增的分子途径是进行再生医学的必要里程碑。在这里,我们使用斑马鱼模型来研究 ckit 信号通路在这个过程中的作用。我们分别展示了 kitb/kitlgb 信号在造血干细胞(HSCs)、造血内皮细胞和尾造血组织(CHT)的特化和扩增中的重要性。此外,我们在斑马鱼基因组中鉴定了骨形态发生蛋白(Oncostatin M,osm)的斑马鱼同源物。我们表明,在造血内皮细胞的特化过程中,osm/osmr 途径位于 kitb 的上游,而这两条途径在 CHT 中协同作用以扩增 HSCs。此外,我们发现 osm 除了促进 HSC 增殖外,还抑制 HSC 向淋巴样命运的分化。总的来说,我们的数据确定了两种由血管龛分泌的细胞因子 kitlgb 和 osm,它们在早期胚胎发育过程中控制 HSCs。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3bd/5993650/fd0ea41c22a3/gr1.jpg

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