脊髓伸长使斑马鱼的后体能按比例调节。

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2025-01-01 Epub Date: 2025-01-09 DOI:10.1242/dev.204438
Dillan Saunders, Carlos Camacho-Macorra, Benjamin Steventon
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引用次数: 0

摘要

早期胚胎显示出调节组织模式的能力,以响应组织大小的变化。然而,尚不清楚这种能力是否会持续到原肠胚形成后阶段。在这里,我们使用多光子消融技术靶向去除斑马鱼尾尾的背祖细胞。这导致脊髓和尾部近轴中胚层的长度成比例减少,揭示了尾巴形成过程中组织形态发生的调节能力。通过对细胞增殖、基因表达、信号传导和细胞运动的分析,我们没有发现细胞命运从中胚层转变为神经命运以弥补神经祖细胞损失的证据。此外,直接去除等量的中胚层祖细胞后,尾近轴中胚层的长度不会减少,从而排除了神经中胚层感受性细胞能够进行比例调节的假设。相反,脊髓细胞数量的减少减少了脊髓和近轴中胚层的长度。我们得出结论,脊髓伸长是斑马鱼尾部近轴中胚层伸长的驱动因素,这可以解释神经祖细胞减少的比例调节。
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Spinal cord elongation enables proportional regulation of the zebrafish posterior body.

Early embryos display a remarkable ability to regulate tissue patterning in response to changes in tissue size. However, it is not clear whether this ability continues into post-gastrulation stages. Here, we performed targeted removal of dorsal progenitors in the zebrafish tailbud using multiphoton ablation. This led to a proportional reduction in the length of the spinal cord and paraxial mesoderm in the tail, revealing a capacity for the regulation of tissue morphogenesis during tail formation. Following analysis of cell proliferation, gene expression, signalling and cell movements, we found no evidence of cell fate switching from mesoderm to neural fate to compensate for neural progenitor loss. Furthermore, tail paraxial mesoderm length is not reduced upon direct removal of an equivalent number of mesoderm progenitors, ruling out the hypothesis that neuromesodermal competent cells enable proportional regulation. Instead, reduction in cell number across the spinal cord reduces both spinal cord and paraxial mesoderm length. We conclude that spinal cord elongation is a driver of paraxial mesoderm elongation in the zebrafish tail and that this can explain proportional regulation upon neural progenitor reduction.

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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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