Evidence map›Paper›PMID 34052998›Full record

ArticleJournal of assisted reproduction and genetics2021

Dysregulation of bisphosphoglycerate mutase during in vitro maturation of oocytes.

Megan Lim, Hannah M Brown, Ryan D Rose, Jeremy G Thompson, Kylie R Dunning

Abstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Article
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  4. Addition of granulocyte macrophage colony stimulating factor (GM-CSF) duringThe Journal of reproduction and development · 2024
    Article
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  6. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Megan LimRobinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0002-9868-429X
Hannah M BrownThe Victorian Heart Institute, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0001-6342-3316
Ryan D RoseRobinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0001-9732-1713
Jeremy G ThompsonRobinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0003-4941-7731
Kylie R DunningRobinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia. kylie.dunning@adelaide.edu.au.ORCID http://orcid.org/0000-0002-0462-6479

Funding

Australian Research Council Centre of Excellence for Nanoscale Biophotonics CE140100003Hospital Research Foundation C-MCF-58-2019National Health and Medical Research Council 1077694
6 · The paper itself

Abstract

purposeOxygen is vital for oocyte maturation; however, oxygen regulation within ovarian follicles is not fully understood. Hemoglobin is abundant within the in vivo matured oocyte, indicating potential function as an oxygen regulator. However, hemoglobin is significantly reduced following in vitro maturation (IVM). The molecule 2,3-bisphosphoglycerate (2,3-BPG) is essential in red blood cells, facilitating release of oxygen from hemoglobin. Towards understanding the role of 2,3-BPG in the oocyte, we characterized gene expression and protein abundance of bisphosphoglycerate mutase (Bpgm), which synthesizes 2,3-BPG, and whether this is altered under low oxygen or hemoglobin addition during IVM.

methodsHemoglobin and Bpgm expression within in vivo matured human cumulus cells and mouse cumulus-oocyte complexes (COCs) were evaluated to determine physiological levels of Bpgm. During IVM, Bpgm gene expression and protein abundance were analyzed in the presence or absence of low oxygen (2% and 5% oxygen) or exogenous hemoglobin.

resultsThe expression of Bpgm was significantly lower than hemoglobin when mouse COCs were matured in vivo. Following IVM at 20% oxygen, Bpgm gene expression and protein abundance were significantly higher compared to in vivo. At 2% oxygen, Bpgm was significantly higher compared to 20% oxygen, while exogenous hemoglobin resulted in significantly lower Bpgm in the COC.

conclusionHemoglobin and 2,3-BPG may play a role within the maturing COC. This study shows that IVM increases Bpgm within COCs compared to in vivo. Decreasing oxygen concentration and the addition of hemoglobin altered Bpgm, albeit not to levels observed in vivo.

Indexed as

In Vitro Oocyte Maturation Techniques2,3-DiphosphoglycerateAnimalsBisphosphoglycerate MutaseBlastocystCumulus CellsFemaleFertilization in VitroGene Expression Regulation, DevelopmentalHumansMeiosisMiceOocytesOogenesisOvarian Follicle2,3-DiphosphoglycerateBisphosphoglycerate Mutase2,3-BisphosphoglycerateBisphosphoglycerate mutaseCumulus-oocyte complexHemoglobinOocyte maturationOxygen

Identifiers

PMID34052998
PMCPMC8266955

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.