Evidence map›Paper›PMID 36201606›Full record

ArticleEndocrinology2022

Follicle-Stimulating Hormone Glycosylation Variants Distinctly Modulate Pre-antral Follicle Growth and Survival.

Gillian P Johnson, Caitlan G A Onabanjo, Kate Hardy, Viktor Y Butnev, George R Bousfield, Kim C Jonas

Open access · hybridAbstract read
In one paragraph

Article in Endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.0field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Gillian P JohnsonDepartment of Women and Children's Health, School of Life Course and Population Health Sciences, Kings College London, London SE1 1UL, UK.ORCID 0000-0002-9224-2992
Caitlan G A OnabanjoDepartment of Women and Children's Health, School of Life Course and Population Health Sciences, Kings College London, London SE1 1UL, UK.
Kate HardyInstitute of Reproductive and Developmental Biology, Imperial College London, London W12 0NN, UK.
Viktor Y ButnevDepartment of Biological Sciences, Wichita State University, Wichita, KS 67260, USA.
George R BousfieldDepartment of Biological Sciences, Wichita State University, Wichita, KS 67260, USA.
Kim C JonasDepartment of Women and Children's Health, School of Life Course and Population Health Sciences, Kings College London, London SE1 1UL, UK.ORCID 0000-0003-1891-2617
King's College London · GBWichita State University · USImperial College London · GB

Funding

The Aging Pituitary/Gonadal AxisP01AG029531 · NIA · WICHITA STATE UNIVERSITY · PI CHITTIBABU GUDA · 2009 to 2026
$25.9M
Biotechnology and Biological Sciences Research Council BB/R015961/1Biotechnology and Biological Sciences Research Council BB/R015961/2NIA NIH HHS P01 AG029531
6 · The paper itself

Abstract

Follicle-stimulating hormone (FSH) is a key endocrine regulator of ovarian function. FSH is secreted as 2 macroglycosylation variants: partially glycosylated FSH (FSH21/18) and fully glycosylated FSH (FSH24). FSH21/18 is more potent than FSH24 at binding to and activating the FSH receptor (R). The ratio of FSH21/18:FSH24 has been shown to change with age, with FSH21/18 predominant at reproductive prime, and FSH24 predominant during perimenopause/menopause. How these FSH glycosylation variants modulate ovarian follicle functions remains largely unknown. The aim of this study was to investigate the effect of FSH glycosylation variants of pre-antral follicle function. Pre-antral follicles were isolated from 3- to 5-week-old C57BL/6 mice and treated ±10 ng/mL FSH21/18, FSH24, a ratio of 80:20 FSH21/18:FSH24 (to mimic reproductive prime), 50:50 FSH21/18:FSH24 (perimenopause), or 20:80 FSH21/18:FSH24 (menopause) for up to 96 hours. FSH21/18 and 80:20 FSH21/18:FSH24 increased follicle growth, in comparison with control, contrasting with FSH24 and 20:80 FSH21/18:FSH24. Survival rates were decreased in follicles treated with FSH24 or 20:80 FSH21/18:FSH24, with follicles undergoing basement membrane rupture and oocyte extrusion, increased Caspase3 gene and protein expression, and decreased markers of cell proliferation in FSH24 or 20:80 FSH21/18:FSH24-treated follicles. Moreover, this correlated with differential regulation of key genes modulating follicular functions. Pharmacological inhibitors of key FSH signal pathways suggests FSH21/18 and FSH24 initiate different FSHR signal pathway activation, which may determine their differential effects on follicle growth and survival. These data suggest that the nature of FSH glycosylation modulates the follicular cellular environment to regulate follicle growth and survival and may underpin the increasing ovarian resistance to FSH observed during aging.

Indexed as

Follicle Stimulating HormoneReceptors, FSHAnimalsFemaleGlycosylationMiceMice, Inbred C57BLOvarian FollicleFollicle Stimulating HormoneReceptors, FSHagingfolliclefollicle stimulating hormonefollicle stimulating hormone receptormenopauseovary

Identifiers

PMID36201606
PMCPMC9598563
OpenAlexW4302763611

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.