Evidence map›Paper›PMID 28927759›Full record

ReviewSeminars in cell & developmental biology2018

Redox stress and signaling during vertebrate embryonic development: Regulation and responses.

Alicia R Timme-Laragy, Mark E Hahn, Jason M Hansen, Archit Rastogi, Monika A Roy

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. The critical role of cardiolipin in metazoan differentiation, development, and maturation.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Review
  9. Article
  10. Reciprocal Regulation of Shh Trafficking and HAntioxidants (Basel, Switzerland) · 2022
    Article
  11. Glucose-6-Phosphate Dehydrogenase, Redox Homeostasis and Embryogenesis.International journal of molecular sciences · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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 at 3 institutions in 1 country.

Alicia R Timme-LaragyDepartment of Environmental Health Sciences, School of Public Health and Health Sciences, University of Massachusetts, Amherst, MA 01003, USA. Electronic address: aliciat@umass.edu.
Mark E HahnBiology Department, Woods Hole Oceanographic Institution, Woods Hole, MA 02543, USA.
Jason M HansenDepartment of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84602, USA.
Archit RastogiMolecular & Cellular Biology Graduate Program, University of Massachusetts, Amherst, MA 01003, USA.
Monika A RoyDepartment of Environmental Health Sciences, School of Public Health and Health Sciences, University of Massachusetts, Amherst, MA 01003, USA; Biotechnology Training Program, University of Massachusetts, Amherst, MA 01003, USA.
University of Massachusetts Amherst · USBrigham Young University · USWoods Hole Oceanographic Institution · US

Funding

Training CoreP42ES007381 · NIEHS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SHERR, DAVID H · 1995 to 2019
$46.1M
Activation of Nrf2 during embryonic development: mechanisms and consequencesR01ES025748 · NIEHS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI Alicia R Timme-Laragy · 2016 to 2026
$4.0M
Biotechnology Training Program in Applied Life SciencesT32GM135096 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI Jeanne Ann Hardy, Ashish A. Kulkarni · 2020 to 2026
$3.9M
Toxicant disruption of receptor-mediated endocytosis in oogenesis and later life metabolic dysfunctionR01ES028201 · NIEHS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI TIMME-LARAGY, ALICIA R · 2017 to 2021
$2.1M
Mechanisms of Embryo Response to Oxidative StressR01ES016366 · NIEHS · WOODS HOLE OCEANOGRAPHIC INSTITUTION · PI HAHN, MARK E · 2009 to 2013
$1.9M
Cellular Engineering Biotechnology Training ProgramT32GM108556 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI HARDY, JEANNE ANN, PEYTON, SHELLY R. · 2015 to 2019
$766k
NIEHS NIH HHS P42 ES007381NIEHS NIH HHS R01 ES016366NIEHS NIH HHS R01 ES025748NIEHS NIH HHS R01 ES028201NIGMS NIH HHS T32 GM108556NIGMS NIH HHS T32 GM135096
6 · The paper itself

Abstract

Vertebrate embryonic development requires specific signaling events that regulate cell proliferation and differentiation to occur at the correct place and the correct time in order to build a healthy embryo. Signaling pathways are sensitive to perturbations of the endogenous redox state, and are also susceptible to modulation by reactive species and antioxidant defenses, contributing to a spectrum of passive vs. active effects that can affect redox signaling and redox stress. Here we take a multi-level, integrative approach to discuss the importance of redox status for vertebrate developmental signaling pathways and cell fate decisions, with a focus on glutathione/glutathione disulfide, thioredoxin, and cysteine/cystine redox potentials and the implications for protein function in development. We present a tissue-specific example of the important role that reactive species play in pancreatic development and metabolic regulation. We discuss NFE2L2 (also known as NRF2) and related proteins, their roles in redox signaling, and their regulation of glutathione during development. Finally, we provide examples of xenobiotic compounds that disrupt redox signaling in the context of vertebrate embryonic development. Collectively, this review provides a systems-level perspective on the innate and inducible antioxidant defenses, as well as their roles in maintaining redox balance during chemical exposures that occur in critical windows of development.

Indexed as

Oxidation-ReductionAnimalsCell DifferentiationCell ProliferationEmbryonic DevelopmentHumansOrganogenesisReactive Oxygen SpeciesReactive Oxygen SpeciesGlutathioneNrf2PancreasRedox proteomicsToxicology

Identifiers

PMID28927759
PMCPMC5650060
OpenAlexW2759236224

What OpenQuestion holds

Textmetadata
LicenceTDM
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.