小鼠内侧前额叶皮层第一层中间神经元的异质性

IF 2.1 4区 医学 Q3 NEUROSCIENCES
Chen Shen, Wanpeng Cui, Wen-Cheng Xiong, Lin Mei
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引用次数: 0

摘要

皮层1层(L1)作为处理远程输入的关键中继。这一层的gaba能抑制性中间神经元(INs) (layer 1 interneurons [L1INs])起抑制门的作用,调节这些输入并调节皮层深层的活动。然而,他们的特点和回路在内侧前额叶皮层(mPFC)仍然知之甚少。利用生物细胞素标记,我们鉴定出mPFC L1INs的三种不同形态类型:神经胶质细胞(NGCs)、细长NGCs (eNGCs)和单束细胞样(sbc样)细胞。全细胞记录揭示了这些亚型之间不同的放电模式:NGCs和eNGCs主要表现为晚尖峰(LS)模式,sbc样细胞表现出更高的非LS (NLS)模式。我们观察到mPFC L1INs之间的电和化学连接。光遗传激活NDNF+ L1INs对深层神经元具有广泛的抑制作用。对锥体神经元(PyNs)和INs的抑制强度表现出层特异性偏好。这些发现强调了L1INs在调节mPFC回路中的功能多样性,并表明它们在支持高阶认知功能方面的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Heterogeneity of Layer 1 Interneurons in the Mouse Medial Prefrontal Cortex

Heterogeneity of Layer 1 Interneurons in the Mouse Medial Prefrontal Cortex

Cortical Layer 1 (L1) acts as a critical relay for processing long-range inputs. GABAergic inhibitory interneurons (INs) in this layer (Layer 1 interneurons [L1INs]) function as inhibitory gates, regulating these inputs and modulating the activity of deeper cortical layers. However, their characteristics and circuits in the medial prefrontal cortex (mPFC) remain poorly understood. Using biocytin labeling, we identified three distinct morphological types of mPFC L1INs: neurogliaform cells (NGCs), elongated NGCs (eNGCs), and single-bouquet cell-like (SBC-like) cells. Whole-cell recordings revealed distinct firing patterns across these subtypes: NGCs and eNGCs predominantly exhibited late-spiking (LS) patterns, and SBC-like cells displayed a higher prevalence of non-LS (NLS) patterns. We observed both electrical and chemical connections among mPFC L1INs. Optogenetic activation of NDNF+ L1INs demonstrated broad inhibitory effects on deeper layer neurons. The strength of inhibition on pyramidal neurons (PyNs) and INs displayed layer-specific preference. These findings highlight the functional diversity of L1INs in modulating mPFC circuits and suggest their potential role in supporting higher order cognitive functions.

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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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