果蝇幼虫抑制回路基序产生运动程序的多样性和可变性。

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
PLoS Biology Pub Date : 2025-04-21 eCollection Date: 2025-04-01 DOI:10.1371/journal.pbio.3003094
Jacob Francis, Caius R Gibeily, William V Smith, Isabel S Petropoulos, Michael Anderson, William J Heitler, Astrid A Prinz, Stefan R Pulver
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引用次数: 0

摘要

神经网络如何产生和调节具有有限细胞成分的运动输出的多样性和可变性?在这里,我们通过探索在节段组织的果蝇幼虫运动系统中,抑制神经元基序在产生运动程序混合物中所起的作用来研究这个问题。我们开发了一个受实验钙成像数据约束的计算模型。该模型包括具有单一电压门控钙电流的单室细胞,它们通过分级兴奋和抑制性突触相互连接。局部兴奋性和抑制性神经元在每个半球形成条件振荡。周围建筑反映了文献中确定的段间和段内连通性主题的关键方面。该模型产生的活动的异时向波概括了虚拟向前和向后运动的关键特征,以及代表虚拟头部扫描的前部区域的双边不对称活动。竞争性命令样基序的输入统计数据,加上检测跨多个片段活动的抑制基序,产生促进运动输出多样性的网络状态,同时防止运动程序中的不适应重叠。总体而言,该模型为连接组学和生理学研究提供了可测试的预测,同时为揭示抑制回路基元如何支撑运动系统多样性和可变性的产生提供了一个平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibitory circuit motifs in Drosophila larvae generate motor program diversity and variability.

How do neural networks generate and regulate diversity and variability in motor outputs with finite cellular components? Here we examine this problem by exploring the role that inhibitory neuron motifs play in generating mixtures of motor programs in the segmentally organised Drosophila larval locomotor system. We developed a computational model that is constrained by experimental calcium imaging data. The model comprises single-compartment cells with a single voltage-gated calcium current, which are interconnected by graded excitatory and inhibitory synapses. Local excitatory and inhibitory neurons form conditional oscillators in each hemisegment. Surrounding architecture reflects key aspects of inter- and intrasegmental connectivity motifs identified in the literature. The model generates metachronal waves of activity that recapitulate key features of fictive forwards and backwards locomotion, as well as bilaterally asymmetric activity in anterior regions that represents fictive head sweeps. The statistics of inputs to competing command-like motifs, coupled with inhibitory motifs that detect activity across multiple segments generate network states that promote diversity in motor outputs, while at the same time preventing maladaptive overlap in motor programs. Overall, the model generates testable predictions for connectomics and physiological studies while providing a platform for uncovering how inhibitory circuit motifs underpin generation of diversity and variability in motor systems.

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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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