Evidence map›Paper›PMID 32751190›Full record

ArticleInternational journal of environmental research and public health2020

Lysine Deprivation during Maternal Consumption of Low-Protein Diets Could Adversely Affect Early Embryo Development and Health in Adulthood.

Lon J Van Winkle, Vasiliy Galat, Philip M Iannaccone

Open access · goldAbstract read
In one paragraph

Article in International journal of environmental research and public health, 2020. 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
0.8field-weighted citation impact, top 30% of its field
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, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Alteration of mFrontiers in genetics · 2022
    Article
  5. Epigenetic Modifications at the Center of the Barker Hypothesis and Their Transgenerational Implications.International journal of environmental research and public health · 2021
    Review
  6. Article
  7. Review
  8. Environmental Exposures around Conception: Developmental Pathways Leading to Lifetime Disease Risk.International journal of environmental research and public health · 2021
    Review
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

3 authors at 2 institutions in 1 country.

Lon J Van WinkleDepartment of Biochemistry, Midwestern University, Downers Grove, IL 60515, USA.ORCID 0000-0002-2223-0419
Vasiliy GalatDepartment of Pathology, Northwestern University Feinberg School of Medicine, Stanley Manne Children's Research Institute and the Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60209, USA.
Philip M IannacconeDepartments of Pediatrics and Pathology, Northwestern University Feinberg School of Medicine and the Lurie Children's Hospital of Chicago, Chicago, IL 60209, USA.
Northwestern University · USRocky Vista University · US

Funding

Identification of Altered Molecular Signature of Down Syndrome iPS CellsRC1HL100168 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CRISPINO, JOHN D, GALAT, VASIL V · 2009 to 2010
$999k
NHLBI NIH HHS RC1 HL100168
6 · The paper itself

Abstract

The conversion of lysine to glutamate is needed for signaling in all plants and animals. In mouse embryonic stem (mES) cells, and probably their progenitors, endogenous glutamate production and signaling help maintain cellular pluripotency and proliferation, although the source of glutamate is yet to be determined. If the source of glutamate is lysine, then lysine deprivation caused by maternal low-protein diets could alter early embryo development and, consequently, the health of the offspring in adulthood. For these reasons, we measured three pertinent variables in human embryonic stem (hES) cells as a model for the inner cell masses of human blastocysts. We found that RNA encoding the alpha-aminoadipic semialdehyde synthase enzyme, which regulates glutamate production from lysine, was highly expressed in hES cells. Moreover, the mean amount of lysine consumed by hES cells was 50% greater than the mean amount of glutamate they produced, indicating that lysine is likely converted to glutamate in these cells. Finally, hES cells expressed RNA encoding at least two glutamate receptors. Since this may also be the case for hES progenitor cells in blastocysts, further studies are warranted to verify the presence of this signaling process in hES cells and to determine whether lysine deprivation alters early mammalian embryo development.

Indexed as

Diet, Protein-RestrictedEmbryonic DevelopmentLysineAdultAnimalsBlastocystCell DifferentiationCell LineHumansMiceLysinebarker hypothesisblastocystembryoembryonic stem cellsglutamate signalinglow-protein dietlysineoffspring

Identifiers

PMID32751190
PMCPMC7432313
OpenAlexW3045954388

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.