Evidence map›Paper›PMID 14736860›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2004

Heterogeneous requirement of NGF for sympathetic target innervation in vivo.

Natalia O Glebova, David D Ginty

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 121 papers.

0numbers the graph read from it
0cells of the map it votes in
121citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

121 citing papers in PubMed, 228 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Hypertension-induced heart failure disrupts cardiac sympathetic innervation.American journal of physiology. Heart and circulatory physiology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Lung dopaminergic nerves facilitate the establishment of TThe Journal of allergy and clinical immunology · 2023
    Article
  16. Article
  17. Article
  18. Eosinophils regulate intra-adipose axonal plasticity.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. Article
  20. Innervation in organogenesis.Current topics in developmental biology · 2022
    Article

61 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Natalia O GlebovaDepartment of Neuroscience, Howard Hughes Medical Institute, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
David D Ginty
Johns Hopkins University · US

Funding

Neurotrophin signals controlling development of the peripheral nervous systemR01NS034814 · NINDS · JOHNS HOPKINS UNIVERSITY · PI GINTY, DAVID D · 1999 to 2015
$3.0M
NINDS NIH HHS R01 NS034814NINDS NIH HHS R01NS34814
6 · The paper itself

Abstract

The neurotrophin nerve growth factor (NGF) plays a crucial role in the development of the sympathetic nervous system. In addition to being required for sympathetic neuron survival in vivo and in vitro, NGF has been shown to mediate axon growth in vitro. The role of NGF in sympathetic axon growth in vivo, however, is not clear because of its requirement for survival. This requirement can be circumvented by a concomitant deletion of Bax, a pro-apoptotic Bcl-2 family member, thus allowing an examination of the role of neurotrophins in axon growth independently of their function in cell survival. Here, we analyzed peripheral sympathetic target organ innervation in mice deficient for both NGF and Bax. In neonatal NGF-/-; Bax-/- mice, sympathetic target innervation was absent in certain organs (such as salivary glands), greatly reduced in others (such as heart), somewhat diminished in a few (such as stomach and kidneys), but not significantly different from control in some (such as trachea). At embryonic day 16.5, peripheral target sympathetic innervation was also reduced in NGF-/-; Bax-/- mice, with analogous variability for different organs. Interestingly, in some organs such as the spleen the precise location at which sympathetic axons become NGF-dependent for growth was evident. We thus show that NGF is required for complete peripheral innervation of both paravertebral and prevertebral sympathetic ganglia targets in vivo independently of its requirement for cell survival. Remarkably, target organs vary widely in their individual NGF requirements for sympathetic innervation.

Indexed as

Proto-Oncogene Proteins c-bcl-2AnimalsAxonsbcl-2-Associated X ProteinGanglia, SympatheticHeartHeterozygoteHomozygoteKidneyMiceMice, Inbred C57BLMice, KnockoutNerve Growth FactorNeuronsOrgan SpecificityPhenotypeBax protein, mousebcl-2-Associated X ProteinNerve Growth FactorProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-2

Identifiers

PMID14736860
PMCPMC6729267
OpenAlexW2121129175

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.