Octopamine signaling regulates the intracellular pattern of the presynaptic active zone scaffold within Drosophila mushroom body neurons.

IF 7.2 1区 生物学 Q1 Agricultural and Biological Sciences
Hongyang Wu, Sayaka Eno, Kyoko Jinnai, Ayako Abe, Kokoro Saito, Yoh Maekawa, Darren W Williams, Nobuhiro Yamagata, Shu Kondo, Hiromu Tanimoto
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Abstract

Neurons can adjust synaptic output according to the postsynaptic partners. However, the target-specific regulation of synaptic structures within individual neurons in the central nervous system remains unresolved. Applying the CRISPR/Cas9-mediated split-GFP tagging, we visualized the endogenous active zone scaffold protein, Bruchpilot (Brp), in specific cells. This technology enabled the spatial characterization of the presynaptic scaffolds only within the Kenyon cells (KCs) of the Drosophila mushroom bodies. We found the patterned accumulation of Brp among the compartments of axon terminals, where a KC synapses onto different postsynaptic neurons. Mechanistically, the localized octopaminergic projections along γ KC terminals regulate this compartmental Brp heterogeneity via Octβ2R and cAMP signaling. We further found that physiological stress, such as food or sleep deprivation reorganizes this intracellular pattern in an octopamine-dependent manner. Such concurrent regulation of local active zone assemblies thus suggests how the mushroom bodies integrate changing physiological states.

章鱼胺信号调节果蝇蘑菇体神经元突触前活性区支架的细胞内模式。
神经元可以根据突触后伙伴调节突触输出。然而,中枢神经系统中单个神经元突触结构的靶向特异性调节仍未得到解决。利用CRISPR/ cas9介导的分裂- gfp标记,我们在特定细胞中可视化了内源性活性区支架蛋白Bruchpilot (Brp)。该技术使突触前支架仅在果蝇蘑菇体的凯尼恩细胞(KCs)内进行空间表征。我们发现Brp在轴突末端的隔室中有模式积累,在那里KC突触连接到不同的突触后神经元。从机制上讲,沿γ KC末端的局部章鱼胺能投射通过oct - β 2r和cAMP信号调节这种区室Brp异质性。我们进一步发现,生理应激,如食物或睡眠剥夺,以一种依赖章鱼胺的方式重组了这种细胞内模式。因此,这种局部活性区组合的同步调节表明了蘑菇体如何整合变化的生理状态。
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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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