The pivotal role of glucose metabolism in determining oocyte developmental competence
- PMID: 20089664
- DOI: 10.1530/REP-09-0345
The pivotal role of glucose metabolism in determining oocyte developmental competence
Abstract
The environment that the cumulus oocyte complex (COC) is exposed to during either in vivo or in vitro maturation (IVM) can have profound effects on the success of fertilisation and subsequent embryo development. Glucose is a pivotal metabolite for the COC and is metabolised by glycolysis, the pentose phosphate pathway (PPP), the hexosamine biosynthesis pathway (HBP) and the polyol pathway. Over the course of oocyte maturation, a large proportion of total glucose is metabolised via the glycolytic pathway to provide substrates such as pyruvate for energy production. Glucose is also the substrate for many cellular functions during oocyte maturation, including regulation of nuclear maturation and redox state via the PPP and for the synthesis of substrates of extracellular matrices (cumulus expansion) and O-linked glycosylation (cell signalling) via the HBP. However, the oocyte is susceptible to glucose concentration-dependent perturbations in nuclear and cytoplasmic maturation, leading to poor embryonic development post-fertilisation. For example, glucose concentrations either too high or too low result in precocious resumption of nuclear maturation. This review will discuss the relevant pathways of glucose metabolism by COCs during in vivo maturation and IVM, including the relative contribution of the somatic and gamete compartments of the COC to glucose metabolism. The consequences of exposing COCs to abnormal glucose concentrations will also be examined, either during IVM or by altered maternal environments, such as during hyperglycaemia induced by diabetes and obesity.
Similar articles
-
Glucose metabolism characterization during mouse in vitro maturation identifies alterations in cumulus cells†.Biol Reprod. 2021 Apr 1;104(4):902-913. doi: 10.1093/biolre/ioab008. Biol Reprod. 2021. PMID: 33480981
-
Pentose phosphate pathway inhibition during in vitro maturation substantially affects the metabolism of bovine COCs and blastocysts.Theriogenology. 2024 Dec;230:72-80. doi: 10.1016/j.theriogenology.2024.09.009. Epub 2024 Sep 10. Theriogenology. 2024. PMID: 39270445
-
Effect of epidermal growth factor-like peptides on the metabolism of in vitro- matured mouse oocytes and cumulus cells.Biol Reprod. 2014 Mar 6;90(3):49. doi: 10.1095/biolreprod.113.115311. Print 2014 Mar. Biol Reprod. 2014. PMID: 24451986
-
Metabolic co-dependence of the oocyte and cumulus cells: essential role in determining oocyte developmental competence.Hum Reprod Update. 2021 Jan 4;27(1):27-47. doi: 10.1093/humupd/dmaa043. Hum Reprod Update. 2021. PMID: 33020823 Review.
-
Metabolism of the bovine cumulus-oocyte complex and influence on subsequent developmental competence.Soc Reprod Fertil Suppl. 2007;64:179-90. doi: 10.5661/rdr-vi-179. Soc Reprod Fertil Suppl. 2007. PMID: 17491147 Review.
Cited by
-
Heavy Metals in Follicular Fluid Affect the Ultrastructure of the Human Mature Cumulus-Oocyte Complex.Cells. 2023 Nov 5;12(21):2577. doi: 10.3390/cells12212577. Cells. 2023. PMID: 37947655 Free PMC article.
-
Mitochondria of Porcine Oocytes Synthesize Melatonin, Which Improves Their In Vitro Maturation and Embryonic Development.Antioxidants (Basel). 2024 Jul 7;13(7):814. doi: 10.3390/antiox13070814. Antioxidants (Basel). 2024. PMID: 39061883 Free PMC article.
-
Effects of increasing lipopolysaccharide concentrations on in vitro developmental competence of ovine oocytes.Anim Reprod. 2020 Jul 7;17(2):e20190125. doi: 10.1590/1984-3143-AR2019-0125. Anim Reprod. 2020. PMID: 32714454 Free PMC article.
-
Towards a Sustainable Reproduction Management of Dairy Sheep: Glycerol-Based Formulations as Alternative to eCG in Milked Ewes Mated at the End of Anoestrus Period.Animals (Basel). 2021 Mar 24;11(4):922. doi: 10.3390/ani11040922. Animals (Basel). 2021. PMID: 33805051 Free PMC article.
-
Mitochondrial metabolic substrate utilization in granulosa cells reflects body mass index and total follicle stimulating hormone dosage in in vitro fertilization patients.J Assist Reprod Genet. 2020 Nov;37(11):2743-2756. doi: 10.1007/s10815-020-01946-9. Epub 2020 Sep 15. J Assist Reprod Genet. 2020. PMID: 32935173 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous