Planar cell polarity zebrafish models of congenital scoliosis reveal underlying defects in notochord morphogenesis.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2024-11-01 Epub Date: 2024-11-12 DOI:10.1242/dev.202829
Mingqin Wang, Sen Zhao, Chenjun Shi, Marie-Claude Guyot, Meijiang Liao, Josephine T Tauer, Bettina M Willie, Nikita Cobetto, Carl-Éric Aubin, Elke Küster-Schöck, Pierre Drapeau, Jitao Zhang, Nan Wu, Zoha Kibar
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Abstract

Congenital scoliosis (CS) is a type of vertebral malformation for which the etiology remains elusive. The notochord is pivotal for vertebrae development, but its role in CS is still understudied. Here, we generated a zebrafish knockout of ptk7a, a planar cell polarity (PCP) gene that is essential for convergence and extension (C&E) of the notochord, and detected congenital scoliosis-like vertebral malformations (CVMs). Maternal zygotic ptk7a mutants displayed severe C&E defects of the notochord. Excessive apoptosis occurred in the malformed notochord, causing a significantly reduced number of vacuolated cells, and compromising the mechanical properties of the notochord. The latter manifested as a less-stiff extracellular matrix along with a significant reduction in the number of the caveolae and severely loosened intercellular junctions in the vacuolated region. These defects led to focal kinks, abnormal mineralization, and CVMs exclusively at the anterior spine. Loss of function of another PCP gene, vangl2, also revealed excessive apoptosis in the notochord associated with CVMs. This study suggests a new model for CS pathogenesis that is associated with defects in notochord C&E and highlights an essential role of PCP signaling in vertebrae development.

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先天性脊柱侧凸的平面细胞极性斑马鱼模型揭示了脊索形态发生的新的潜在缺陷。
先天性脊柱侧凸(CS)是一种脊椎畸形,其病因至今仍难以确定。脊索是脊椎发育的关键,但它在脊柱侧凸中的作用仍未得到充分研究。ptk7a是一种平面细胞极性(PCP)基因,对脊索的收敛和伸展(C&E)至关重要,斑马鱼敲除ptk7a后会出现先天性脊柱侧弯样脊椎畸形(CVM)。母体子代ptk7a突变体显示出严重的脊索C&E缺陷。畸形的脊索发生过度凋亡,导致空泡细胞数量显著减少,并损害了脊索的机械性能。后者表现为细胞外基质硬度降低,空泡化区域的洞穴数量显著减少,细胞间连接严重松弛。这些缺陷导致局灶性扭结、异常矿化和前脊柱CVM。另一个 PCP 基因 vangl2 的功能缺失也揭示了与 CVM 相关的脊索过度凋亡。这项研究提出了一种与脊索C&E缺陷相关的CS发病新模式,并强调了PCP信号在脊椎发育中的重要作用。
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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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