» Articles » PMID: 30608586

Neurotrophins and Glial Cell Line-derived Neurotrophic Factor in the Ovary: Physiological and Pathophysiological Implications

Overview
Date 2019 Jan 5
PMID 30608586
Citations 55
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Neurotrophins [nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3), and neurotrophin-4 (NT-4)] and glial cell line-derived neurotrophic factor (GDNF) are soluble polypeptide growth factors that are widely recognized for their roles in promoting cell growth, survival and differentiation in several classes of neurons. Outside the nervous system, neurotrophin (NT) and GDNF signaling events have substantial roles in various non-neural tissues, including the ovary.

Objective And Rationale: The molecular mechanisms that promote and regulate follicular development and oocyte maturation have been extensively investigated. However, most information has been obtained from animal models. Even though the fundamental process is highly similar across species, the paracrine regulation of ovarian function in humans remains poorly characterized. Therefore, this review aims to summarize the expression and functional roles of NTs and GDNF in human ovarian biology and disorders, and to describe and propose the development of novel strategies for diagnosing, treating and preventing related abnormalities.

Search Methods: Relevant literature in the English language from 1990 to 2018 describing the role of NTs and GDNF in mammalian ovarian biology and phenotypes was comprehensively selected using PubMed, MEDLINE and Google Scholar.

Outcomes: Studies have shown that the neurotrophins NGF, BDNF, NT-3 and NT-4 as well as GDNF and their functional receptors are expressed in the human ovary. Recently, gathered experimental data suggest putative roles for NT and GDNF signaling in the direct control of ovarian function, including follicle assembly, activation of the primordial follicles, follicular growth and development, oocyte maturation, steroidogenesis, ovulation and corpus luteum formation. Additionally, crosstalk occurs between these ovarian regulators and the endocrine signaling system. Dysregulation of the NT system may negatively affect ovarian function, leading to reproductive pathology (decreased ovarian reserve, polycystic ovary syndrome and endometriosis), female infertility and even epithelial ovarian cancers.

Wider Implications: A comprehensive understanding of the expression, actions and underlying molecular mechanisms of the NT/GDNF system in the human ovary is essential for novel approaches to therapeutic and diagnostic interventions in ovarian diseases and to develop more safe, effective methods of inducing ovulation in ART in the treatment of female infertility.

Citing Articles

Maternal environmental enrichment affects the corpora lutea and progesterone levels in pregnant mice.

De la Cruz Borthiry F, Beltrame J, Schander J, Silva A, Parborell F, Franchi A Front Endocrinol (Lausanne). 2025; 16:1483893.

PMID: 39996056 PMC: 11847664. DOI: 10.3389/fendo.2025.1483893.


Deciphering pain: molecular mechanisms and neurochemical pathways-challenges and future opportunities.

Dehghan B, Abolhasanzadeh N, Shademan B, Nourazarian A Front Mol Biosci. 2024; 11:1382555.

PMID: 39629040 PMC: 11613041. DOI: 10.3389/fmolb.2024.1382555.


The Impact of the Endocrine and Immunological Function of Adipose Tissue on Reproduction in Women with Obesity.

Maczka K, Stasiak O, Przybysz P, Grymowicz M, Smolarczyk R Int J Mol Sci. 2024; 25(17).

PMID: 39273337 PMC: 11395521. DOI: 10.3390/ijms25179391.


Single‑cell RNA sequencing analysis of human embryos from the late Carnegie to fetal development.

Wang C, Wang X, Wang W, Chen Y, Chen H, Wang W Cell Biosci. 2024; 14(1):118.

PMID: 39267141 PMC: 11395182. DOI: 10.1186/s13578-024-01302-9.


Promotes Sheep Granulosa Cells Proliferation and Reproductive Hormone Secretion and Activates the PI3K/AKT Pathway.

Jia Y, Liu Y, Wang P, Liu Z, Zhang R, Chu M Animals (Basel). 2024; 14(10).

PMID: 38791682 PMC: 11117346. DOI: 10.3390/ani14101465.


References
1.
Airaksinen M, Titievsky A, Saarma M . GDNF family neurotrophic factor signaling: four masters, one servant?. Mol Cell Neurosci. 1999; 13(5):313-25. DOI: 10.1006/mcne.1999.0754. View

2.
TRUPP M, Scott R, Whittemore S, Ibanez C . Ret-dependent and -independent mechanisms of glial cell line-derived neurotrophic factor signaling in neuronal cells. J Biol Chem. 1999; 274(30):20885-94. DOI: 10.1074/jbc.274.30.20885. View

3.
Hamanoue M, Middleton G, Wyatt S, Jaffray E, Hay R, Davies A . p75-mediated NF-kappaB activation enhances the survival response of developing sensory neurons to nerve growth factor. Mol Cell Neurosci. 1999; 14(1):28-40. DOI: 10.1006/mcne.1999.0770. View

4.
Vaillant A, Mazzoni I, Tudan C, Boudreau M, Kaplan D, Miller F . Depolarization and neurotrophins converge on the phosphatidylinositol 3-kinase-Akt pathway to synergistically regulate neuronal survival. J Cell Biol. 1999; 146(5):955-66. PMC: 2169479. DOI: 10.1083/jcb.146.5.955. View

5.
Zundel W, Swiersz L, Giaccia A . Caveolin 1-mediated regulation of receptor tyrosine kinase-associated phosphatidylinositol 3-kinase activity by ceramide. Mol Cell Biol. 2000; 20(5):1507-14. PMC: 85322. DOI: 10.1128/MCB.20.5.1507-1514.2000. View