Evidence map›Paper›PMID 29045838›Full record

ArticleCell reports2017

p75 Is Required for the Establishment of Postnatal Sensory Neuron Diversity by Potentiating Ret Signaling.

Zhijiang Chen, Christopher R Donnelly, Bertha Dominguez, Yoshinobu Harada, Weichun Lin, Alan S Halim, Tasha G Bengoechea, Brian A Pierchala, Kuo-Fen Lee

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Metabolic Control of Sensory Neuron Survival by the p75 Neurotrophin Receptor in Schwann Cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  7. In vivo functions of p75Trends in pharmacological sciences · 2021
    Review
  8. The development of somatosensory neurons: Insights into pain and itch.Current topics in developmental biology · 2021
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  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

9 authors at 3 institutions in 2 countries.

Zhijiang ChenThe Salk Institute, Peptide Biology Laboratories, La Jolla, CA 92037, USA.
Christopher R DonnellyDepartment of Biologic and Materials Sciences, University of Michigan, Ann Arbor, MI 48109, USA.
Bertha DominguezThe Salk Institute, Peptide Biology Laboratories, La Jolla, CA 92037, USA.
Yoshinobu HaradaThe Salk Institute, Peptide Biology Laboratories, La Jolla, CA 92037, USA; National Institute of Radiological Sciences and National Institutes for Quantum and Radiological Science and Technology, Chiba 243-8555, Japan.
Weichun LinUT Southwestern Medical Center, Neuroscience, Dallas, TX 75390, USA.
Alan S HalimDepartment of Biologic and Materials Sciences, University of Michigan, Ann Arbor, MI 48109, USA.
Tasha G BengoecheaThe Salk Institute, Peptide Biology Laboratories, La Jolla, CA 92037, USA.
Brian A PierchalaDepartment of Biologic and Materials Sciences, University of Michigan, Ann Arbor, MI 48109, USA. Electronic address: pierchal@umich.edu.
Kuo-Fen LeeThe Salk Institute, Peptide Biology Laboratories, La Jolla, CA 92037, USA. Electronic address: klee@salk.edu.
Salk Institute for Biological Studies · USUniversity of Michigan–Ann Arbor · USSouthwestern Medical Center

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Reuben Shaw · 1985 to 2026
$82.8M
Viral VectorsP01AG010435 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TUSZYNSKI, MARK H. · 1991 to 2014
$20.9M
Growth factors in the development and physiology of geniculate taste neuronsR01DC015799 · NIDCD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Brian Anthony Pierchala · 2017 to 2026
$4.8M
GENETIC ANALYSIS OF ERBB2 IN MAMMALIAN DEVELOPMENTR01HD034534 · NICHD · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI LEE, KUO-FEN · 1996 to 2011
$4.3M
Salk Institute for Biological Studies NINDS Center Core GrantP30NS072031 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI GOULDING, MARTYN D · 2011 to 2015
$4.2M
A p75/Ret Receptor Complex as an Integrator of Survival and DeathR01NS089585 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PIERCHALA, BRIAN ANTHONY · 2015 to 2024
$3.9M
Physiology and function of basal ganglia subcircuits in sequence learningR01NS083815 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI LEE, KUO-FEN · 2013 to 2022
$3.8M
Development of marmoset models of neurodegenerative disease using embryonic stem cell-based gene-editing approachesR24OD023076 · OD · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI LEE, KUO-FEN, REYNOLDS, JOHN H · 2017 to 2020
$3.1M
Optogenetic dissection of brain network deficits in Alzheimer's DiseaseRF1AG047669 · NIA · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI JIN, XIN, LEE, KUO-FEN · 2014 to 2015
$2.2M
Genetic analysis of the neurotrophin receptor p75 in neural developmentR01NS060833 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI LEE, KUO-FEN · 2008 to 2012
$2.1M
Exploring Human-Induced Pluripotent Stem Cells for Alzheimer's Disease ResearchRF1AG042985 · NIA · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI GAGE, FRED H, LEE, KUO-FEN · 2012 to 2012
$528k
Understanding the Function of GFL-Ret Signaling in the Development of the PeripheF30DE023479 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DONNELLY, CHRISTOPHER RYAN · 2014 to 2017
$189k
NCI NIH HHS P30 CA014195NIA NIH HHS P01 AG010435NIA NIH HHS RF1 AG042985NIA NIH HHS RF1 AG047669NICHD NIH HHS R01 HD034534NIDCD NIH HHS R01 DC015799NIDCR NIH HHS F30 DE023479NIH HHS R24 OD023076NINDS NIH HHS P30 NS072031NINDS NIH HHS R01 NS060833NINDS NIH HHS R01 NS083815NINDS NIH HHS R01 NS089585
6 · The paper itself

Abstract

Producing the neuronal diversity required to adequately discriminate all elements of somatosensation is a complex task during organogenesis. The mechanisms guiding this process during dorsal root ganglion (DRG) sensory neuron specification remain poorly understood. Here, we show that the p75 neurotrophin receptor interacts with Ret and its GFRα co-receptor upon stimulation with glial cell line-derived neurotrophic factor (GDNF). Furthermore, we demonstrate that p75 is required for GDNF-mediated Ret activation, survival, and cell surface localization of Ret in DRG neurons. In mice in which p75 is deleted specifically within sensory neurons beginning at E12.5, we observe that approximately 20% of neurons are lost between P14 and adulthood, and these losses selectively occur within a subpopulation of Ret

Indexed as

Signal TransductionAnimalsAnimals, NewbornCell MembraneCell SurvivalCore Binding Factor Alpha 2 SubunitGanglia, SpinalGlial Cell Line-Derived Neurotrophic FactorGlial Cell Line-Derived Neurotrophic Factor ReceptorsIntegrasesLigandsMiceNociceptionNociceptorsPeptidesProto-Oncogene Proteins c-retCore Binding Factor Alpha 2 SubunitCre recombinaseGfra1 protein, mouseGlial Cell Line-Derived Neurotrophic FactorGlial Cell Line-Derived Neurotrophic Factor ReceptorsIntegrasesLigandsPeptidesProto-Oncogene Proteins c-retReceptor, Nerve Growth Factordorsal root ganglionGDNFnociceptive neuronnonpeptidergicp75Ret

Identifiers

PMID29045838
PMCPMC5705950
OpenAlexW2766781430

What OpenQuestion holds

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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.