Transcriptome profiling of kisspeptin neurons from the mouse arcuate nucleus reveals new mechanisms in estrogenic control of fertility.

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License: CC BY-NC-ND 4.0
Serval ID
serval:BIB_008517AC197F
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Transcriptome profiling of kisspeptin neurons from the mouse arcuate nucleus reveals new mechanisms in estrogenic control of fertility.
Journal
Proceedings of the National Academy of Sciences of the United States of America
Author(s)
Göcz B., Rumpler É., Sárvári M., Skrapits K., Takács S., Farkas I., Csillag V., Trinh S.H., Bardóczi Z., Ruska Y., Solymosi N., Póliska S., Szőke Z., Bartoloni L., Zouaghi Y., Messina A., Pitteloud N., Anderson R.C., Millar R.P., Quinton R., Manchishi S.M., Colledge W.H., Hrabovszky E.
ISSN
1091-6490 (Electronic)
ISSN-L
0027-8424
Publication state
Published
Issued date
05/07/2022
Peer-reviewed
Oui
Volume
119
Number
27
Pages
e2113749119
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Abstract
Kisspeptin neurons in the mediobasal hypothalamus (MBH) are critical targets of ovarian estrogen feedback regulating mammalian fertility. To reveal molecular mechanisms underlying this signaling, we thoroughly characterized the estrogen-regulated transcriptome of kisspeptin cells from ovariectomized transgenic mice substituted with 17β-estradiol or vehicle. MBH kisspeptin neurons were harvested using laser-capture microdissection, pooled, and subjected to RNA sequencing. Estrogen treatment significantly (p.adj. < 0.05) up-regulated 1,190 and down-regulated 1,139 transcripts, including transcription factors, neuropeptides, ribosomal and mitochondrial proteins, ion channels, transporters, receptors, and regulatory RNAs. Reduced expression of the excitatory serotonin receptor-4 transcript (Htr4) diminished kisspeptin neuron responsiveness to serotonergic stimulation. Many estrogen-regulated transcripts have been implicated in puberty/fertility disorders. Patients (n = 337) with congenital hypogonadotropic hypogonadism (CHH) showed enrichment of rare variants in putative CHH-candidate genes (e.g., LRP1B, CACNA1G, FNDC3A). Comprehensive characterization of the estrogen-dependent kisspeptin neuron transcriptome sheds light on the molecular mechanisms of ovary-brain communication and informs genetic research on human fertility disorders.
Keywords
Animals, Arcuate Nucleus of Hypothalamus/metabolism, Estrogens/metabolism, Female, Fertility/genetics, Gene Expression Profiling, Humans, Hypogonadism/congenital, Hypogonadism/genetics, Kisspeptins/genetics, Kisspeptins/metabolism, Mice, Mice, Transgenic, Neurons/metabolism, Ovary/metabolism, RNA sequencing, fertility, gene expression, neuropeptides, reproduction
Pubmed
Web of science
Open Access
Yes
Create date
13/07/2022 12:51
Last modification date
25/01/2024 8:30
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