Molecular basis of reproductive senescence: insights from model organisms.


Journal

Journal of assisted reproduction and genetics
ISSN: 1573-7330
Titre abrégé: J Assist Reprod Genet
Pays: Netherlands
ID NLM: 9206495

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 17 08 2020
accepted: 25 09 2020
pubmed: 3 10 2020
medline: 2 7 2021
entrez: 2 10 2020
Statut: ppublish

Résumé

Reproductive decline due to parental age has become a major barrier to fertility as couples have delayed having offspring into their thirties and forties. Advanced parental age is also associated with increased incidence of neurological and cardiovascular disease in offspring. Thus, elucidating the etiology of reproductive decline is of clinical importance. Deciphering the underlying processes that drive reproductive decline is particularly challenging in women in whom a discrete oocyte pool is established during embryogenesis and may remain dormant for tens of years. Instead, our understanding of the processes that drive reproductive senescence has emerged from studies in model organisms, both vertebrate and invertebrate, that are the focus of this literature review. Studies of reproductive aging in model organisms not only have revealed the detrimental cellular changes that occur with age but also are helping identify major regulator proteins controlling them. Here, we discuss what we have learned from model organisms with respect to the molecular mechanisms that maintain both genome integrity and oocyte quality.

Identifiants

pubmed: 33006069
doi: 10.1007/s10815-020-01959-4
pii: 10.1007/s10815-020-01959-4
pmc: PMC7822982
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

17-32

Subventions

Organisme : NIA NIH HHS
ID : R56 AG066682
Pays : United States
Organisme : National Institute of General Medical Sciences (US)
ID : R01GM104007
Organisme : NIA NIH HHS
ID : R01 AG051659
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM104007
Pays : United States
Organisme : National Institute on Aging (US)
ID : R01AG051659

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Auteurs

Cristina Quesada-Candela (C)

Magee-Womens Research Institute, Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh School of Medicine, 204 Craft Avenue, Pittsburgh, PA, 15213, USA.

Julia Loose (J)

Departments of Pediatrics, Developmental Biology and Cell Biology and Physiology, John G. Rangos Sr. Research Center, University of Pittsburgh School of Medicine, Room 7129, One Children's Hospital Drive, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.

Arjumand Ghazi (A)

Departments of Pediatrics, Developmental Biology and Cell Biology and Physiology, John G. Rangos Sr. Research Center, University of Pittsburgh School of Medicine, Room 7129, One Children's Hospital Drive, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.

Judith L Yanowitz (JL)

Magee-Womens Research Institute, Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh School of Medicine, 204 Craft Avenue, Pittsburgh, PA, 15213, USA. yanowitzjl@mwri.magee.edu.

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