Notochord segmentation in zebrafish controlled by iterative mechanical signaling

IF 10.7 1区 生物学 Q1 CELL BIOLOGY
Susan Wopat, Priyom Adhyapok, Bijoy Daga, Janice M. Crawford, James Norman, Jennifer Bagwell, Brianna Peskin, Indrasen Magre, Stephanie M. Fogerson, Daniel S. Levic, Stefano Di Talia, Daniel P. Kiehart, Patrick Charbonneau, Michel Bagnat
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Abstract

In bony fishes, patterning of the vertebral column, or spine, is guided by a metameric blueprint established in the notochord sheath. Notochord segmentation begins days after somitogenesis concludes and can occur in its absence. However, somite patterning defects lead to imprecise notochord segmentation, suggesting that these processes are linked. Here, we identify that interactions between the notochord and the axial musculature ensure precise spatiotemporal segmentation of the zebrafish spine. We demonstrate that myoseptum-notochord linkages drive notochord segment initiation by locally deforming the notochord extracellular matrix and recruiting focal adhesion machinery at these contact points. Irregular somite patterning alters this mechanical signaling, causing non-sequential and dysmorphic notochord segmentation, leading to altered spine development. Using a model that captures myoseptum-notochord interactions, we find that a fixed spatial interval is critical for driving sequential segment initiation. Thus, mechanical coupling of axial tissues facilitates spatiotemporal spine patterning.

Abstract Image

斑马鱼的脊索节段受迭代机械信号控制
在骨鱼中,脊椎柱或脊柱的形态是由在脊索鞘中建立的元蓝图引导的。在体节发生结束几天后,脊索开始分节,在没有脊索的情况下也会发生分节。然而,体节模式化缺陷会导致不精确的脊索分节,这表明这些过程是相互关联的。在这里,我们发现脊索和轴肌之间的相互作用确保了斑马鱼脊柱的精确时空分割。我们证明,肌膜-脊索连接通过使脊索细胞外基质局部变形并在这些接触点招募焦点粘附机制来驱动脊索节段的启动。不规则的体节模式改变了这种机械信号传递,导致无序和畸形的脊索分节,从而导致脊柱发育改变。利用捕捉肌隔膜-脊索相互作用的模型,我们发现固定的空间间隔对于驱动有序的节段启动至关重要。因此,轴组织的机械耦合促进了脊柱的时空模式化。
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来源期刊
Developmental cell
Developmental cell 生物-发育生物学
CiteScore
18.90
自引率
1.70%
发文量
203
审稿时长
3-6 weeks
期刊介绍: Developmental Cell, established in 2001, is a comprehensive journal that explores a wide range of topics in cell and developmental biology. Our publication encompasses work across various disciplines within biology, with a particular emphasis on investigating the intersections between cell biology, developmental biology, and other related fields. Our primary objective is to present research conducted through a cell biological perspective, addressing the essential mechanisms governing cell function, cellular interactions, and responses to the environment. Moreover, we focus on understanding the collective behavior of cells, culminating in the formation of tissues, organs, and whole organisms, while also investigating the consequences of any malfunctions in these intricate processes.
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