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再生涡虫身体模式轴的神经控制。

Neural control of body-plan axis in regenerating planaria.

机构信息

Allen Discovery Center, Tufts University, Medford, Massachusetts, United States of America.

Department of Biology, Tufts University, Medford, Massachusetts, United States of America.

出版信息

PLoS Comput Biol. 2019 Apr 16;15(4):e1006904. doi: 10.1371/journal.pcbi.1006904. eCollection 2019 Apr.

DOI:10.1371/journal.pcbi.1006904
PMID:30990801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6485777/
Abstract

Control of axial polarity during regeneration is a crucial open question. We developed a quantitative model of regenerating planaria, which elucidates self-assembly mechanisms of morphogen gradients required for robust body-plan control. The computational model has been developed to predict the fraction of heteromorphoses expected in a population of regenerating planaria fragments subjected to different treatments, and for fragments originating from different regions along the anterior-posterior and medio-lateral axis. This allows for a direct comparison between computational and experimental regeneration outcomes. Vector transport of morphogens was identified as a fundamental requirement to account for virtually scale-free self-assembly of the morphogen gradients observed in planarian homeostasis and regeneration. The model correctly describes altered body-plans following many known experimental manipulations, and accurately predicts outcomes of novel cutting scenarios, which we tested. We show that the vector transport field coincides with the alignment of nerve axons distributed throughout the planarian tissue, and demonstrate that the head-tail axis is controlled by the net polarity of neurons in a regenerating fragment. This model provides a comprehensive framework for mechanistically understanding fundamental aspects of body-plan regulation, and sheds new light on the role of the nervous system in directing growth and form.

摘要

再生过程中轴向极性的控制是一个悬而未决的关键问题。我们开发了一种再生涡虫的定量模型,该模型阐明了形态发生梯度的自组装机制,这些机制对于稳健的身体计划控制是必需的。该计算模型用于预测在经历不同处理的再生涡虫碎片群体中预期的异型发生的分数,以及来自沿前后轴和左右轴的不同区域的碎片。这允许在计算和实验再生结果之间进行直接比较。形态发生素的向量运输被确定为基本要求,以解释在涡虫体内平衡和再生中观察到的形态发生素梯度的几乎无标度自组装。该模型正确描述了许多已知实验操作后的身体计划改变,并准确预测了我们测试的新型切割方案的结果。我们表明,向量运输场与分布在整个涡虫组织中的神经轴突的排列一致,并证明在再生片段中,头部-尾部轴由神经元的净极性控制。该模型为从机械角度理解身体计划调节的基本方面提供了一个综合框架,并为神经系统在指导生长和形态形成中的作用提供了新的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/34fd79881dd6/pcbi.1006904.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/dca89d64e6db/pcbi.1006904.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/b13975beb460/pcbi.1006904.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/6a1fe5dc7de1/pcbi.1006904.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/f2e69d90cdae/pcbi.1006904.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/43fcde64ed3a/pcbi.1006904.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/3d28b480303e/pcbi.1006904.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/34fd79881dd6/pcbi.1006904.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/dca89d64e6db/pcbi.1006904.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/b13975beb460/pcbi.1006904.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/6a1fe5dc7de1/pcbi.1006904.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/f2e69d90cdae/pcbi.1006904.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/43fcde64ed3a/pcbi.1006904.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/3d28b480303e/pcbi.1006904.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a88/6485777/34fd79881dd6/pcbi.1006904.g007.jpg

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Bioelectrical control of positional information in development and regeneration: A review of conceptual and computational advances.生物电控制发育和再生中的位置信息:概念和计算进展综述。
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A Novel Perspective on Neuronal Control of Anatomical Patterning, Remodeling, and Maintenance.一种关于神经元控制解剖结构形成、重塑和维持的新视角。
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