小鼠脑内7个kisspeptin神经元群的综合化学解剖图谱和性腺调节。

IF 3.3 4区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Vito S. Hernández, Mario A. Zetter, Oscar R. Hernández-Pérez, Rafael Hernández-González, Ignacio Camacho-Arroyo, Robert P. Millar, Lee E. Eiden, Limei Zhang
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引用次数: 0

摘要

Kisspeptinergic信号被认为是调节生殖的关键,但它在大脑功能中潜在的更广泛的作用却鲜为人知。本研究探讨了表达kisspeptin的神经元在小鼠脑内的分布和化学分型。采用RNAscope单、双和多重原位杂交方法,评估kisspeptin mRNA (Kiss1)的表达及其与其他神经肽、兴奋性和抑制性神经递质标记物和性类固醇受体的共表达。7种不同的kisspeptin神经元化学型被表征,包括两个新的kisspeptin表达组首次被描述,即Kiss1群体在腹侧乳头前核和孤立束核。Kiss1 mRNA也被观察到定位于下丘脑神经元的体细胞和树突状区室。雄激素受体的高表达以及内侧杏仁核和中隔下丘脑Kiss1在GDX后的表达变化表明雄激素受体在调节kisspeptin信号传导中起作用,而在女性中则没有。这项研究提供了表达kisspeptin的神经元的详细化学解剖图谱,突出了它们潜在的功能多样性。新的kisspeptin表达组的发现和性腺切除术引起的Kiss1表达模式的变化表明,kisspeptin在生殖之外的脑功能中具有更广泛的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comprehensive chemoanatomical mapping, and the gonadal regulation, of seven kisspeptin neuronal populations in the mouse brain

Comprehensive chemoanatomical mapping, and the gonadal regulation, of seven kisspeptin neuronal populations in the mouse brain

Kisspeptinergic signaling is well-established as crucial for the regulation of reproduction, but its potential broader role in brain function is less understood. This study investigates the distribution and chemotyping of kisspeptin-expressing neurons within the mouse brain. RNAscope single, dual, and multiplex in situ hybridization methods were used to assess kisspeptin mRNA (Kiss1) expression and its co-expression with other neuropeptides, excitatory and inhibitory neurotransmitter markers, and sex steroid receptors in wild-type intact and gonadectomized young adult mice. Seven distinct kisspeptin neuronal chemotypes were characterized, including two novel kisspeptin-expressing groups described for the first time, that is, the Kiss1 population in the ventral premammillary nucleus and the nucleus of the solitary tract. Kiss1 mRNA was also observed to localize in both somatic and dendritic compartments of hypothalamic neurons. High androgen receptor expression and changes in medial amygdala and septo-hypothalamic Kiss1 expression following GDX in males, but not in females, suggest a role for androgen receptors in regulating kisspeptin signaling. This study provides a detailed chemoanatomical map of kisspeptin-expressing neurons, highlighting their potential functional diversity. The discovery of a new kisspeptin-expressing group and gonadectomy-induced changes in Kiss1 expression patterns suggest broader roles for kisspeptin in brain functions beyond those of reproduction.

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来源期刊
Journal of Neuroendocrinology
Journal of Neuroendocrinology 医学-内分泌学与代谢
CiteScore
6.40
自引率
6.20%
发文量
137
审稿时长
4-8 weeks
期刊介绍: Journal of Neuroendocrinology provides the principal international focus for the newest ideas in classical neuroendocrinology and its expanding interface with the regulation of behavioural, cognitive, developmental, degenerative and metabolic processes. Through the rapid publication of original manuscripts and provocative review articles, it provides essential reading for basic scientists and clinicians researching in this rapidly expanding field. In determining content, the primary considerations are excellence, relevance and novelty. While Journal of Neuroendocrinology reflects the broad scientific and clinical interests of the BSN membership, the editorial team, led by Professor Julian Mercer, ensures that the journal’s ethos, authorship, content and purpose are those expected of a leading international publication.
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