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斑马鱼肌节中背侧细胞等同群内的形态发生和细胞命运决定。

Morphogenesis and cell fate determination within the adaxial cell equivalence group of the zebrafish myotome.

机构信息

Australian Regenerative Medicine Institute, Monash University, Clayton, Australia.

出版信息

PLoS Genet. 2012;8(10):e1003014. doi: 10.1371/journal.pgen.1003014. Epub 2012 Oct 25.

Abstract

One of the central questions of developmental biology is how cells of equivalent potential-an equivalence group-come to adopt specific cellular fates. In this study we have used a combination of live imaging, single cell lineage analyses, and perturbation of specific signaling pathways to dissect the specification of the adaxial cells of the zebrafish embryo. We show that the adaxial cells are myogenic precursors that form a cell fate equivalence group of approximately 20 cells that consequently give rise to two distinct sub-types of muscle fibers: the superficial slow muscle fibers (SSFs) and muscle pioneer cells (MPs), distinguished by specific gene expression and cell behaviors. Using a combination of live imaging, retrospective and indicative fate mapping, and genetic studies, we show that MP and SSF precursors segregate at the beginning of segmentation and that they arise from distinct regions along the anterior-posterior (AP) and dorsal-ventral (DV) axes of the adaxial cell compartment. FGF signaling restricts MP cell fate in the anterior-most adaxial cells in each somite, while BMP signaling restricts this fate to the middle of the DV axis. Thus our results reveal that the synergistic actions of HH, FGF, and BMP signaling independently create a three-dimensional (3D) signaling milieu that coordinates cell fate within the adaxial cell equivalence group.

摘要

发育生物学的核心问题之一是如何使具有相同潜能的细胞——即等同群细胞——获得特定的细胞命运。在这项研究中,我们综合运用活体成像、单细胞谱系分析以及特定信号通路的干扰等方法,解析了斑马鱼胚胎顶端细胞的特化过程。我们发现,顶端细胞是成肌前体细胞,它们形成了大约 20 个细胞的细胞命运等同群,随后分化为两种不同类型的肌肉纤维:浅层慢肌纤维(SSFs)和肌肉先驱细胞(MPs),这两种细胞通过特定的基因表达和细胞行为来区分。我们利用活体成像、回溯和指示性命运映射以及遗传研究的方法,发现 MP 和 SSF 前体细胞在体节形成的早期就已经开始分化,并且它们起源于沿顶端细胞区的前后(AP)和背腹(DV)轴的不同区域。FGF 信号在每个体节的最前端顶端细胞中限制 MP 细胞命运,而 BMP 信号则将这种命运限制在 DV 轴的中间。因此,我们的结果揭示了 HH、FGF 和 BMP 信号的协同作用独立地创建了一个三维(3D)信号微环境,协调了顶端细胞等同群内的细胞命运。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a5b/3486873/47f594db245b/pgen.1003014.g001.jpg

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