脊髓损伤和未损伤情况下控制小鼠尿道外括约肌的脊髓神经回路的性别二态性

IF 2.3 4区 医学 Q3 NEUROSCIENCES
Sergei Karnup, Mamoru Hashimoto, Kang Jun Cho, Jonathan Beckel, William de Groat, Naoki Yoshimura
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引用次数: 0

摘要

脊髓损伤(SCI)会破坏膀胱和尿道外括约肌(EUS)之间的协调,导致一过性或永久性排尿障碍,男性的情况更为严重。男性与女性在与EUS相关的脊髓回路中的差异以及SCI后的重新布线对于了解性/性别特异性障碍和可能的恢复机制至关重要。为了定量评估雄性与雌性、脊髓完好(SI)与SCI动物EUS回路之间的差异,我们逆行追踪并计数了EUS相关神经元。在转基因 ChAT-GFP 小鼠中,用注射到 EUS 的 PRV614-red 荧光蛋白(RFP)逆向追踪运动神经元(MNs)、中间神经元(INs)和本体脊髓神经元(PPNs)。通过使用荧光金(FG)对背外侧核(DLN)中的 EUS-MNs 与其他 GFP+ MNs 进行追踪,将它们与其他 GFP+ MNs 区分开来。我们在 DLN 中发现了两种形态不同的细胞类型:FG+纺锤形双极(SB-MNs)和 FG- 圆形多极(RM-MNs)胆碱能细胞。男性两种类型的胆碱能细胞数量都是女性的两倍。脊髓损伤导致所有脊髓核中的MNs部分丧失。脊髓损伤后,雄性支配后肢的后DLN(RDLN)中RFP标记细胞的数量增加了四倍。这表明:(a)脊髓核团之间存在直接的突触相互作用;(b)SCI 后其他运动核团对 EUS-MNs 的非特异性输入增加。雄性和雌性之间的 INs 和 PPNs 数量有所延迟:在SI男性中,INs和PPNs的数量是SI女性的10倍。损伤导致雄性 INs 和 PPNs 减少两倍,而雌性则没有。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Sexual Dimorphism of Spinal Neural Circuits Controlling the Mouse External Urethral Sphincter With and Without Spinal Cord Injury

Sexual Dimorphism of Spinal Neural Circuits Controlling the Mouse External Urethral Sphincter With and Without Spinal Cord Injury

Spinal cord injury (SCI) disrupts coordination between the bladder and the external urinary sphincter (EUS), leading to transient or permanent voiding impairment, which is more severe in males. Male versus female differences in spinal circuits related to the EUS as well as post-SCI rewiring are essential for understanding of sex-/gender-specific impairments and possible recovery mechanisms. To quantitatively assess differences between EUS circuits in males versus females and in spinal intact (SI) versus SCI animals, we retrogradely traced and counted EUS-related neurons. In transgenic ChAT-GFP mice, motoneurons (MNs), interneurons (INs), and propriospinal neurons (PPNs) were retrogradely trans-synaptically traced with PRV614-red fluorescent protein (RFP) injected into EUS. EUS-MNs in dorsolateral nucleus (DLN) were separated from other GFP+ MNs by tracing them with FluoroGold (FG). We found two morphologically distinct cell types in DLN: FG+ spindle-shaped bipolar (SB-MNs) and FG rounded multipolar (RM-MNs) cholinergic cells. Number of MNs of both types in males was twice as large as in females. SCI caused a partial loss of MNs in all spinal nuclei. After SCI, males showed a fourfold rise in the number of RFP-labeled cells in retro-DLN (RDLN) innervating hind limbs. This suggests (a) an existence of direct synaptic interactions between spinal nuclei and (b) a post-SCI increase of non-specific inputs to EUS-MNs from other motor nuclei. Number of INs and PPNs deferred between males and females: In SI males, the numbers of INs and PPNs were ∼10 times larger than in SI females. SCI caused a twofold decrease of INs and PPNs in males but not in females.

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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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