Evidence map›Paper›PMID 29671738›Full record

ArticleeLife2018

HIF-2α is essential for carotid body development and function.

David Macias, Andrew S Cowburn, Hortensia Torres-Torrelo, Patricia Ortega-Sáenz, José López-Barneo, Randall S Johnson

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Hif-2α programs oxygen chemosensitivity in chromaffin cells.The Journal of clinical investigation · 2024
    Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Constitutive Expression of Hif2α Confers Acute OAdvances in experimental medicine and biology · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. Oxygen regulation of breathing is abolished in mitochondrial complex III-deficient arterial chemoreceptors.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 3 countries.

David MaciasDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0002-8676-1964
Andrew S CowburnDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Hortensia Torres-TorreloInstituto de Biomedicina de Sevilla, Seville, Spain.
Patricia Ortega-SáenzInstituto de Biomedicina de Sevilla, Seville, Spain.
José López-BarneoInstituto de Biomedicina de Sevilla, Seville, Spain.
Randall S JohnsonDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0002-4084-6639
Instituto de Biomedicina de Sevilla · ESUniversity of Cambridge · GB

Funding

Wellcome TrustWellcome Trust WT092738
6 · The paper itself

Abstract

Mammalian adaptation to oxygen flux occurs at many levels, from shifts in cellular metabolism to physiological adaptations facilitated by the sympathetic nervous system and carotid body (CB). Interactions between differing forms of adaptive response to hypoxia, including transcriptional responses orchestrated by the Hypoxia Inducible transcription Factors (HIFs), are complex and clearly synergistic. We show here that there is an absolute developmental requirement for HIF-2α, one of the HIF isoforms, for growth and survival of oxygen sensitive glomus cells of the carotid body. The loss of these cells renders mice incapable of ventilatory responses to hypoxia, and this has striking effects on processes as diverse as arterial pressure regulation, exercise performance, and glucose homeostasis. We show that the expansion of the glomus cells is correlated with mTORC1 activation, and is functionally inhibited by rapamycin treatment. These findings demonstrate the central role played by HIF-2α in carotid body development, growth and function.

Indexed as

Cell DifferentiationAnimalsBasic Helix-Loop-Helix ProteinsCarotid BodyEndothelial PAS Domain-Containing Protein 1MiceBasic Helix-Loop-Helix ProteinsEndothelial PAS Domain-Containing Protein 1carotid bodycomputational biologyhypoxiamousesympathetic nervessystems biology

Identifiers

PMID29671738
PMCPMC5916566
OpenAlexW2787575237

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.