Evidence map›Paper›PMID 26074780›Full record

ArticleFrontiers in neuroanatomy2015

Impact of a deletion of the full-length and short isoform of p75NTR on cholinergic innervation and the population of postmitotic doublecortin positive cells in the dentate gyrus.

Robert Poser, Martin Dokter, Viola von Bohlen Und Halbach, Stefan M Berger, Ruben Busch, Marian Baldus, Klaus Unsicker, Oliver von Bohlen Und Halbach

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroanatomy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Neurotrophic Factors and Dendritic Spines.Advances in neurobiology · 2023
    Article
  6. Article
  7. Article
  8. PROneurotrophins and CONSequences.Molecular neurobiology · 2018
    Review
  9. Review
  10. Review
  11. Article
  12. 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

8 authors at 2 institutions in 1 country.

Robert PoserInstitute of Anatomy and Cell Biology, Universitätsmedizin Greifswald Greifswald, Germany.
Martin DokterInstitute of Anatomy and Cell Biology, Universitätsmedizin Greifswald Greifswald, Germany.
Viola von Bohlen Und HalbachInstitute of Anatomy and Cell Biology, Universitätsmedizin Greifswald Greifswald, Germany.
Stefan M BergerDepartment of Molecular Biology, Central Institute of Mental Health and Medical Faculty Mannheim, Heidelberg University Mannheim, Germany.
Ruben BuschInstitute of Anatomy and Cell Biology, Universitätsmedizin Greifswald Greifswald, Germany.
Marian BaldusInstitute of Anatomy and Cell Biology, Universitätsmedizin Greifswald Greifswald, Germany.
Klaus UnsickerDepartment of Molecular Embryology, Institute of Anatomy and Cell Biology, University of Freiburg Freiburg, Germany.
Oliver von Bohlen Und HalbachInstitute of Anatomy and Cell Biology, Universitätsmedizin Greifswald Greifswald, Germany.
Universitätsmedizin Greifswald · DEUniversity Hospital Heidelberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Analyses of mice carrying a deletion of the pan-neurotrophin receptor p75NTR have allowed identifying p75NTR as an important structural regulator of the hippocampus. Most of the previous analyses were done using p75NTR (ExIII) knockout mice which still express the short isoform of p75NTR. To scrutinize the role of p75NTR in the hippocampus, we analyzed adult and aged p75NTR (ExIV) knockout mice, in which both, the short and the full-length isoform are deleted. Deletion of these isoforms induced morphological alterations in the adult dentate gyrus (DG), leading to an increase in the thickness of the molecular and granular layer. Based on these observations, we next determined the morphological substrates that might contribute to this phenotype. The cholinergic innervation of the molecular and granular layer of the DG was found to be significantly increased in the knockout mice. Furthermore, adult neurogenesis in the DG was found to be significantly altered with increased numbers of doublecortin (DCX) positive cells and reduced numbers of apoptotic cells in p75NTR (ExIV) knockout mice. However, cell proliferation as measured by phosphohiston H3 (PH3) positive cell numbers was not affected. These morphological alterations (number of DCX-positive cells and increased cholinergic fiber densities) as well as reduced cell death in the DG are likely to contribute to the observed thickening of the granular layer in p75NTR (ExIV) knockout mice. In addition, Sholl-analysis of DCX-positive neurons revealed a higher dendritic complexity and could thus be a possible morphological correlate for the increased thickness of the molecular layer in p75NTR deficient animals. Our data clearly demonstrate that deletion of both, the short and the full-length isoform of p75NTR affects DG morphology, due to alterations of the cholinergic system and an imbalance between neurogenesis and programmed cell death within the subgranular zone.

Indexed as

adult neurogenesischolinergic systemdendritic spineneurotrophinp75NTR

Identifiers

PMID26074780
PMCPMC4444824
OpenAlexW1568185780

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Registered trials

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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.