Transcriptome-scale spatial gene expression in rat arcuate nucleus during puberty.
Transcriptome-scale spatial gene expression in rat arcuate nucleus during puberty.
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青春期大鼠弓状核转录组规模的空间基因表达
DOI:
10.1186/s13578-022-00745-2
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发表时间:
2022-01-21
影响因子:
7.5
通讯作者:
Shen Y
中科院分区:
文献类型:
--
作者:
Zhou S;Zang S;Hu Y;Shen Y;Li H;Chen W;Li P;Shen Y
A variety of neurons in hypothalamus undergo a complicated regulation on transcription activity of multiple genes for hypothalamic–pituitary–gonadal axis activation during pubertal development. Identification of puberty-associated cell composition and characterization of the unique transcriptional signatures across different cells are beneficial to isolation of specific neurons and advanced understanding of their functions. The hypothalamus of female Sprague–Dawley rats in postnatal day-25, 35 and 45 were used to define the dynamic spatial atlas of gene expression in the arcuate nucleus (ARC) by 10× Genomics Visium platform. A surface protein expressed selectively by kisspeptin neurons was used to sort neurons by flow cytometric assay in vitro. The transcriptome of the isolated cells was examined using Smart sequencing. Four subclusters of neurons with similar gene expression signatures in ARC were identified. Only one subcluster showed the robust expression of Kiss1, which could be isolated by a unique membrane surface biomarker Solute carrier family 18 member A3 (SLC18A3). Moreover, genes in different subclusters presenting three expression modules distinctly functioned in each pubertal stage. Different types of cells representing distinct functions on glial or neuron differentiation, hormone secretion as well as estradiol response precisely affect and coordinate with each other, resulting in a complicated regulatory network for hypothalamic–pituitary–gonadal axis initiation and modulation. Our data revealed a comprehensive transcriptomic overview of ARC within different pubertal stages, which could serve as a valuable resource for the study of puberty and sexual development disorders. The online version contains supplementary material available at 10.1186/s13578-022-00745-2.
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影响因子:
2.7
作者:
Barroso, Alexia;Roa, Juan;Tena-Sempere, Manuel
通讯作者:
Tena-Sempere, Manuel
DOI:
10.1210/me.2012-1371
发表时间:
2013-04
期刊:
Molecular endocrinology (Baltimore, Md.)
影响因子:
--
作者:
Atkin SD;Owen BM;Bookout AL;Cravo RM;Lee C;Elias CF;Elmquist JK;Kliewer SA;Mangelsdorf DJ
通讯作者:
Mangelsdorf DJ
影响因子:
56.9
作者:
Stahl, Patrik L.;Salmen, Fredrik;Frisen, Jonas
通讯作者:
Frisen, Jonas
影响因子:
2
作者:
Xu, Jing;Li, Pin
通讯作者:
Li, Pin
影响因子:
3.7
作者:
Shen Y;Zhou S;Zhao X;Li H;Sun J
通讯作者:
Sun J