从两节到更长:调查马拉喹鲤的再生起始阶段。

IF 2.6 3区 生物学 Q2 DEVELOPMENTAL BIOLOGY
Vanessa Spieß, Rannyele P. Ribeiro, Conrad Helm, M. Teresa Aguado
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引用次数: 0

摘要

无脊椎动物具有多种多样的再生能力,但完全的全身再生并不常见,尤其是头部和身体前部的再生。本研究对Syllis malaquini的再生能力进行了详细的形态学描述。通过复制以前的实验和执行不同的手术程序,我们探索了该物种的全身再生能力。我们详细说明了眼睛、颚骨、咽齿、颈部器官和身体色素等特定结构在截肢后再生的精确时间。我们的高分辨率扫描电子显微镜和共聚焦激光扫描显微镜图像提供了胚泡区的细节,揭示了肛门口与外部环境保持联系,而口腔开口则是在胚泡分化过程中 "重新 "形成的。此外,我们还进行了截肢,从肠道躯干区域分离出由一个、两个和三个节段组成的片段。我们发现,S. malaquini 至少需要两到三个节段才能成功再生整个身体。此外,我们还验证了肠道区域不同,再生能力也不同,前肠的结构极大地影响了再生过程的某些步骤。我们的研究填补了有关肠道形成及其对再生能力影响的知识空白。持续的研究对于揭示肠道组织特异性和可塑性在无脊椎动物,尤其是节肢动物再生过程中的作用至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

From two segments and beyond: Investigating the onset of regeneration in Syllis malaquini

From two segments and beyond: Investigating the onset of regeneration in Syllis malaquini

Annelids feature a diverse range of regenerative abilities, but complete whole-body regeneration is less common, particularly in the context of the head and anterior body regeneration. This study provides a detailed morphological description of Syllis malaquini regenerative abilities. By replicating previous experiments and performing diverse surgical procedures, we explored the capacity of this species for whole-body regeneration. We detailed the precise timing of regeneration of particular structures such as the eyes, proventricle, pharyngeal tooth, nuchal organs, and body pigmentation after amputation. Our high-resolution scanning electron microscopy and confocal laser-scanning microscopy images provide details of the blastema region, revealing that while anal opening remains in connection to the exterior environment, oral opening is formed “de novo” during blastema differentiation. Additionally, we performed amputations to isolate fragments consisting of one, two, and three segments from the intestinal trunk region. We found that S. malaquini requires at least two to three segments to successfully regenerate the whole body. In addition, we verified a variable capacity to regenerate depending upon the gut region, with structures of the foregut greatly impairing some steps of the regenerative process. Our work notably addresses the gap in knowledge concerning gut formation and its impact on regenerative capabilities. Ongoing research is crucial to unravel the role of gut tissue specificity and plasticity during regeneration in annelids, and particularly in syllids.

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来源期刊
Evolution & Development
Evolution & Development 生物-发育生物学
CiteScore
6.30
自引率
3.40%
发文量
26
审稿时长
>12 weeks
期刊介绍: Evolution & Development serves as a voice for the rapidly growing research community at the interface of evolutionary and developmental biology. The exciting re-integration of these two fields, after almost a century''s separation, holds much promise as the focus of a broader synthesis of biological thought. Evolution & Development publishes works that address the evolution/development interface from a diversity of angles. The journal welcomes papers from paleontologists, population biologists, developmental biologists, and molecular biologists, but also encourages submissions from professionals in other fields where relevant research is being carried out, from mathematics to the history and philosophy of science.
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