Insulin Reduces Reaction of Follicular Granulosa Cells to FSH Stimulation in Women With Obesity-Related Infertility During IVF.


Journal

The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362

Informations de publication

Date de publication:
01 07 2019
Historique:
received: 30 03 2018
accepted: 16 11 2018
pubmed: 27 11 2018
medline: 28 5 2020
entrez: 27 11 2018
Statut: ppublish

Résumé

Women with obesity usually need larger doses of FSH for ovarian stimulation, resulting in poor outcomes; however, the mechanism is still unclear. To investigate the molecular regulation of FSH receptor (FSHR) expression associated with obesity. Case-control study to improve in vitro fertilization (IVF) outcomes. Women with obesity (82) and women who were overweight (457) undergoing IVF and 1790 age-matched controls with normal weight from our reproductive medicine center. FSHR expression was decreased in parallel with body mass index (BMI), whereas the estradiol (E2) level on the human chorionic gonadotropin (hCG) trigger day was significantly lower. FSHR expression in human granulosa cells (hGCs), both mRNA (P = 0.02) and protein (P = 0.001) levels, was decreased in women who were overweight or obese. Both insulin (P < 0.001) and glucose (P = 0.0017) levels were positively correlated with BMI in fasting blood and follicle fluids (FFs) but not with FFs leptin level. We treated human granulosa-like tumor cells (KGN) cells with insulin; E2 production was compromised; the level of phosphorylated (p)-protein kinase B (p-Akt2) decreased, whereas p-glycogen synthase kinase 3 (GSK3) increased; and there were similar changes in hGCs from women with obesity. Stimulated hGCs from women with obesity with compound 21 (CP21), an inhibitor of GSK3β, resulted in upregulated β-catenin activation and increased FSHR expression. CP21 also increased the expression of insulin receptor substrate 1 and phosphatidylinositol 3-kinase (PI3K), as well as p-Akt2. Women with obesity in IVF were associated with reduced FSHR expression and E2 production caused by a dysfunctional insulin pathway. Decreased FSHR expression in hGCs from women with obesity and insulin-treated KGN cells could be rescued by an inhibitor of GSK3β, which might be a potential target for the improvement of the impaired FSH-stimulation response in women with obesity.

Identifiants

pubmed: 30476103
pii: 5193471
doi: 10.1210/jc.2018-00686
doi:

Substances chimiques

Insulin 0
Leptin 0
Receptors, FSH 0
Estradiol 4TI98Z838E
Follicle Stimulating Hormone 9002-68-0
GSK3B protein, human EC 2.7.11.1
Glycogen Synthase Kinase 3 beta EC 2.7.11.1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2547-2560

Informations de copyright

Copyright © 2019 Endocrine Society.

Auteurs

Pei Xu (P)

Key Laboratory for Major Obstetric Diseases of Guangdong Province, Key Laboratory of Reproduction and Genetics of Guangdong Higher Education Institutes, Reproductive Medicine Center of the Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

Bao-Yi Huang (BY)

Key Laboratory for Major Obstetric Diseases of Guangdong Province, Key Laboratory of Reproduction and Genetics of Guangdong Higher Education Institutes, Reproductive Medicine Center of the Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

Jia-Hui Zhan (JH)

Key Laboratory for Major Obstetric Diseases of Guangdong Province, Key Laboratory of Reproduction and Genetics of Guangdong Higher Education Institutes, Reproductive Medicine Center of the Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

Man-Ting Liu (MT)

Key Laboratory for Major Obstetric Diseases of Guangdong Province, Key Laboratory of Reproduction and Genetics of Guangdong Higher Education Institutes, Reproductive Medicine Center of the Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

Yang Fu (Y)

Key Laboratory for Major Obstetric Diseases of Guangdong Province, Key Laboratory of Reproduction and Genetics of Guangdong Higher Education Institutes, Reproductive Medicine Center of the Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

You-Qiang Su (YQ)

State Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.

Qing-Yuan Sun (QY)

State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.

Wei-Hua Wang (WH)

Houston Fertility Institute/New Houston Health, Houston, Texas.

Dun-Jin Chen (DJ)

Key Laboratory for Major Obstetric Diseases of Guangdong Province, Key Laboratory of Reproduction and Genetics of Guangdong Higher Education Institutes, Reproductive Medicine Center of the Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

Jian-Qiao Liu (JQ)

Key Laboratory for Major Obstetric Diseases of Guangdong Province, Key Laboratory of Reproduction and Genetics of Guangdong Higher Education Institutes, Reproductive Medicine Center of the Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

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Classifications MeSH