Timing Matters: Lessons From Perinatal Neurogenesis in the Olfactory Bulb

IF 2.1 4区 医学 Q3 NEUROSCIENCES
Teresa Liberia, Kimberly Han, Natalie J. Spence, Sarah J. Meller, Eduardo Martin-Lopez, Charles A. Greer
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Abstract

In the olfactory bulb (OB), odorant receptor-specific input converges into glomeruli. Subsequently, the coding of odor information is fine-tuned by local synaptic circuits within the glomeruli and the deeper external plexiform layer (EPL) in the OB. Deciphering the organization of inhibitory granule cells (GCs) in the EPL relative to the secondary dendrites of projection neurons is pivotal for understanding odor processing. We conducted a detailed investigation of GCs, focusing on the timing of neurogenesis, laminar distribution, and synaptogenesis between GCs and projection neurons. In summary, GCs develop following a developmental continuum with an outside-in maturation pattern from embryogenesis to adulthood. GCs born 1 week after birth display a unique sublayer-specific distribution pattern, marking a transition between embryonic or neonatal and adult stages. Integration into reciprocal synaptic circuits occurred 10 days post-neurogenesis. We conclude that the timing of neurogenesis dictates the anatomical configuration of GCs within the OB, which, in turn, regulates preferential synaptic integration with either mitral cell or tufted cell secondary dendrites.

Abstract Image

时间问题:从围产期嗅球神经发生的经验教训
在嗅球(OB)中,气味受体特异性输入汇聚到肾小球。随后,气味信息的编码通过肾小球和OB中更深的外丛状层(EPL)内的局部突触回路进行微调。破译EPL中相对于投射神经元次级树突的抑制颗粒细胞(GCs)的组织是理解气味加工的关键。我们对GCs进行了详细的研究,重点研究了神经发生的时间、层流分布以及GCs与投射神经元之间的突触发生。总之,从胚胎发生到成年,GCs的发育遵循一个由外而内的成熟模式。出生后1周出生的GCs显示出独特的亚层特异性分布模式,标志着胚胎或新生儿和成人阶段之间的过渡。在神经发生后10天,突触会整合到相互的突触回路中。我们的结论是,神经发生的时间决定了OB内GCs的解剖结构,这反过来又调节了与二尖瓣细胞或簇状细胞次级树突的优先突触整合。
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来源期刊
CiteScore
5.80
自引率
8.00%
发文量
158
审稿时长
3-6 weeks
期刊介绍: Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states. Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se. JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.
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