Oxidative Stress Induces Telomere Dysfunction and Shortening in Human Oocytes of Advanced Age Donors

Research from the past decades provided strong evidence that in humans the pool of oocytes starts to decline already before the birth of a female individual, and from menarche to menopause the oocyte is exposed to different environmental stimuli. Since more and more women of the 21st century in deve...

Full description

Bibliographic Details
Main Author: Paweł Kordowitzki
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Cells
Subjects:
ROS
Online Access:https://www.mdpi.com/2073-4409/10/8/1866
id doaj-6260b3b3a2ea411d87d7d35cf0dc9293
record_format Article
spelling doaj-6260b3b3a2ea411d87d7d35cf0dc92932021-08-26T13:36:54ZengMDPI AGCells2073-44092021-07-01101866186610.3390/cells10081866Oxidative Stress Induces Telomere Dysfunction and Shortening in Human Oocytes of Advanced Age DonorsPaweł Kordowitzki0Institute of Animal Reproduction and Food Research of Polish Academy of Sciences, Tuwima Street 10, 10-243 Olsztyn, PolandResearch from the past decades provided strong evidence that in humans the pool of oocytes starts to decline already before the birth of a female individual, and from menarche to menopause the oocyte is exposed to different environmental stimuli. Since more and more women of the 21st century in developed countries wish to postpone the first pregnancy to their thirties, higher rates of miscarriage and chromosomal non-disjunction might occur. In oocytes of advanced maternal age, meaning above 35 years of age, characteristics such as chromosomal instabilities/abnormalities, spindle defects, decreased mitochondrial function and telomere shortening become more prevalent than in younger counterparts. Telomere attrition belongs to the so-called “hallmarks of aging” which are also relevant for the female germ-line cells. In oocytes, telomeres shorten with advancing maternal age due to the effects of reactive oxygen species and not upon replicative senescence, similar to how it is common in dividing cells.https://www.mdpi.com/2073-4409/10/8/1866oxidative stressROStelomereschromosome instabilityoocytesaging
collection DOAJ
language English
format Article
sources DOAJ
author Paweł Kordowitzki
spellingShingle Paweł Kordowitzki
Oxidative Stress Induces Telomere Dysfunction and Shortening in Human Oocytes of Advanced Age Donors
Cells
oxidative stress
ROS
telomeres
chromosome instability
oocytes
aging
author_facet Paweł Kordowitzki
author_sort Paweł Kordowitzki
title Oxidative Stress Induces Telomere Dysfunction and Shortening in Human Oocytes of Advanced Age Donors
title_short Oxidative Stress Induces Telomere Dysfunction and Shortening in Human Oocytes of Advanced Age Donors
title_full Oxidative Stress Induces Telomere Dysfunction and Shortening in Human Oocytes of Advanced Age Donors
title_fullStr Oxidative Stress Induces Telomere Dysfunction and Shortening in Human Oocytes of Advanced Age Donors
title_full_unstemmed Oxidative Stress Induces Telomere Dysfunction and Shortening in Human Oocytes of Advanced Age Donors
title_sort oxidative stress induces telomere dysfunction and shortening in human oocytes of advanced age donors
publisher MDPI AG
series Cells
issn 2073-4409
publishDate 2021-07-01
description Research from the past decades provided strong evidence that in humans the pool of oocytes starts to decline already before the birth of a female individual, and from menarche to menopause the oocyte is exposed to different environmental stimuli. Since more and more women of the 21st century in developed countries wish to postpone the first pregnancy to their thirties, higher rates of miscarriage and chromosomal non-disjunction might occur. In oocytes of advanced maternal age, meaning above 35 years of age, characteristics such as chromosomal instabilities/abnormalities, spindle defects, decreased mitochondrial function and telomere shortening become more prevalent than in younger counterparts. Telomere attrition belongs to the so-called “hallmarks of aging” which are also relevant for the female germ-line cells. In oocytes, telomeres shorten with advancing maternal age due to the effects of reactive oxygen species and not upon replicative senescence, similar to how it is common in dividing cells.
topic oxidative stress
ROS
telomeres
chromosome instability
oocytes
aging
url https://www.mdpi.com/2073-4409/10/8/1866
work_keys_str_mv AT pawełkordowitzki oxidativestressinducestelomeredysfunctionandshorteninginhumanoocytesofadvancedagedonors
_version_ 1721194365874864128