Evidence map›Paper›PMID 22074716›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2012

Divergent postnatal development of the carotid body in DBA/2J and A/J strains of mice.

Eric W Kostuk, Alexander Balbir, Koichi Fujii, Akiko Fujioka, Luis E Pichard, Machiko Shirahata

Open access · greenAbstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Carotid chemoreceptor development in mice.Respiratory physiology & neurobiology · 2013
    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

6 authors at 1 institution in 1 country.

Eric W KostukDepartment of Environmental Health Sciences, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205, USA.
Alexander Balbir
Koichi Fujii
Akiko Fujioka
Luis E Pichard
Machiko Shirahata
Johns Hopkins University · US

Funding

Chemoreceptor Cell Development in the Carotid BodyR01HL081345 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI SHIRAHATA, MACHIKO · 2007 to 2011
$1.8M
Modulation of Voltage-gated K Channels in Glomus CellsR01HL072293 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI SHIRAHATA, MACHIKO · 2003 to 2006
$975k
NHLBI NIH HHS HL-72293NHLBI NIH HHS HL-81345
6 · The paper itself

Abstract

We have previously shown that the adult DBA/2J and A/J strains of mice differ in carotid body volume and morphology. The question has arisen whether these differences develop during the prenatal or postnatal period. Investigating morphological development of the carotid body and contributing genes in these mice can provide further understanding of the appropriate formation of the carotid body. We examined the carotid body of these mice from 1 day to 4 wk old for differences in volume, morphology, and gene expression of Gdnf family, Dlx2, Msx2, and Phox2b. The two strains showed divergent morphology starting at 1 wk old. The volume of the carotid body increased from 1 wk up to 2 wk old to the level of 4 wk old in the DBA/2J mice but not in the A/J mice. This corresponds with immunoreactivity of LC3, an autophagy marker, in A/J tissues at 10 days and 2 wk. The differences in gene expression were examined at 1 wk, 10 days, and 2 wk old, because divergent growth occurred during this period. The DBA/2J's carotid body at 1 wk old showed a greater expression of Msx2 than the A/J's carotid body. No other candidate genes showed consistent differences between the ages and strains. The difference was not seen in sympathetic cervical ganglia of 1 wk old, suggesting that the difference is carotid body specific. The current study indicates the critical postnatal period for developing distinctive morphology of the carotid body in these mice. Further studies are required to further elucidate a role of Msx2 and other uninvestigated genes.

Indexed as

AnimalsCarotid BodyGanglia, SympatheticGene ExpressionGlial Cell Line-Derived Neurotrophic FactorsHomeodomain ProteinsMaleMiceMice, Inbred DBAMicrotubule-Associated ProteinsSuperior Cervical GanglionTranscription FactorsDistal-less homeobox proteinsGlial Cell Line-Derived Neurotrophic FactorsHomeodomain ProteinsMap1lc3b protein, mouseMicrotubule-Associated ProteinsMSX2 proteinNBPhox proteinTranscription Factors

Identifiers

PMID22074716
PMCPMC3289426
OpenAlexW2055462909

What OpenQuestion holds

Textmetadata
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.