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  5. Dynamics of IGF signalling during the ovulatory peak in women undergoing ovarian stimulation
 
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Dynamics of IGF signalling during the ovulatory peak in women undergoing ovarian stimulation
File(s)
IGF-paper (ovulatory peak) (JAB) (Sep2021)JCEM[32].pdf (923.06 KB)
Accepted version
Author(s)
Botkjaer, Jane Alro
Poulsen, Liv la Cour
Noer, Pernille Rimmer
Grondahl, Marie Louise
Englund, Anne Lis Mikkelsen
more
Type
Journal Article
Abstract
Context
Insulin-like growth factor (IGF) signaling is known to affect human ovarian follicular function during growth and development. However, the role of the IGF system is unknown during the ovulatory peak, which is characterized by profound changes in granulosa cell (GCs) mitosis and function.

Objective
How is the IGF system expressed and regulated during the midcycle surge in women?

Methods
Follicular fluid (FF) and GCs were collected during the ovulatory peak from 2 specific time points. One sample was obtained before oocyte pickup (OPU): before ovulation trigger (OT) (T = 0 hours) or at 12, 17, or 32 hours after OT, and 1 sample was obtained at OPU 36 hours after OT. Fifty women undergoing ovarian stimulation at a university hospital were included. Gene expression profiles were assessed by microarray analysis of GCs. IGF-related proteins in the FF were assessed by immunoassay or by determination of activity with a proteinase assay.

Results
Gene expression of proteins promoting IGF activity (ie, IGF2, PAPP-A, and IRS1) together with proliferation markers were downregulated on a transcriptional level in GCs after OT, whereas proteins inhibiting the IGF signal (ie, IGFBPs, IGF2, and STC1) were upregulated. STC1 gene expression and protein levels were greatly upregulated after OT with a parallel steep downregulation of PAPP-A proteolytic activity.

Conclusion
These data suggest that downregulation of IGF signaling mediated by increased STC1 expression is instrumental for the sudden cessation in GC proliferation and onset of differentiation during the ovulatory peak.
Date Issued
2025-01
Date Acceptance
2024-02-29
Citation
Journal of Clinical Endocrinology and Metabolism, 2025, 110 (1), pp.e160-e167
URI
http://hdl.handle.net/10044/1/115261
URL
https://doi.org/10.1210/clinem/dgae132
DOI
https://www.dx.doi.org/10.1210/clinem/dgae132
ISSN
0021-972X
Publisher
Oxford University Press
Start Page
e160
End Page
e167
Journal / Book Title
Journal of Clinical Endocrinology and Metabolism
Volume
110
Issue
1
Copyright Statement
© The Author(s) 2024. Published by Oxford University Press on behalf of the Endocrine Society. This is the author’s accepted manuscript made available under a CC-BY licence in accordance with Imperial’s Research Publications Open Access policy (www.imperial.ac.uk/oa-policy)
License URL
http://creativecommons.org/licenses/by/4.0/
Identifier
https://doi.org/10.1210/clinem/dgae132
Subjects
AKT
Endocrinology & Metabolism
EXPRESSION
granulosa cells
GRANULOSA-CELLS
GROWTH-FACTORS
HORMONE
human ovarian follicles
IGF signaling
INSULIN-RECEPTOR ISOFORM
Life Sciences & Biomedicine
ovulation
PAPP-A
PLASMA-PROTEIN-A
PROTEOLYTIC ACTIVITY
Science & Technology
STANNIOCALCIN-1
stanniocalcins
Publication Status
Published
Article Number
dgae132
Date Publish Online
2024-03-04
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