Allometry in limb regeneration and scale-invariant patterning as the basis of normal morphogenesis from different sizes of blastemas.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Development Pub Date : 2024-09-30 DOI:10.1242/dev.202697
Saya Furukawa, Sakiya Yamamoto, Ayaka Ohashi, Yoshihiro Morishita, Akira Satoh
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引用次数: 0

Abstract

Axolotl (Ambystoma mexicanum) limb regeneration begins with blastemas of various sizes, in contrast to the limb developmental process. Despite this size variation, normal limb morphology, consistent with a limb stump size, is regenerated. This outcome suggests the existence of underlying scale-invariant mechanisms. To identify such mechanisms, we examined the allometric relationships between blastema size, and Sonic Hedgehog (Shh) and Fibroblast Growth Factor 8 (Fgf8) expression patterns against limb stump size. We found that all factors showed allometric rather than isometric scaling; specifically, their relative sizes decrease with an increase in limb stump size. However, the ratio of Shh/Fgf8 signaling dominant region was nearly constant, independent of blastema/body size. Furthermore, the relative spatial patterns of cell density and proliferation activity and the relative position of first digit formation were scale-invariant in the summed Shh/Fgf8 crosstalk region. This scale-invariant nature may underlie the morphogenesis of normal limbs from different sizes of blastemas.

肢体再生中的异型性和规模不变模式化是不同大小胚胎正常形态发生的基础。
Axolotl(Ambystoma mexicanum)肢体再生始于不同大小的胚泡,这与肢体发育过程形成鲜明对比。尽管存在这种大小差异,但仍能再生出与肢体残端大小一致的正常肢体形态。这一结果表明存在着潜在的规模不变机制。为了确定这种机制,我们研究了胚泡大小、音速刺猬(Shh)和成纤维细胞生长因子8(Fgf8)表达模式与肢体残端大小之间的异速关系。我们发现,所有因子都呈现出等比(而非等距)缩放关系;具体来说,它们的相对大小随着肢体残端大小的增加而减小。然而,Shh/Fgf8 信号主导区域的比例几乎是恒定的,与胚泡/体型大小无关。此外,Shh/Fgf8串扰总和区域的细胞密度和增殖活动的相对空间模式以及第一位数形成的相对位置与尺度无关。这种尺度不变性可能是不同大小胚泡形成正常肢体的形态发生的基础。
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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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