Evidence map›Paper›PMID 15056704›Full record

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

A transgenic marker for newly born granule cells in dentate gyrus.

Linda S Overstreet, Shane T Hentges, Viviana F Bumaschny, Flavio S J de Souza, James L Smart, Andrea M Santangelo, Malcolm J Low, Gary L Westbrook, Marcelo Rubinstein

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 114 papers.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed
4.9field-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

114 citing papers in PubMed, 206 citations in OpenAlex.

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54 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

9 authors at 3 institutions in 3 countries.

Linda S OverstreetVollum Institute, Oregon Health and Science University, Portland, Oregon 97239, USA. overstre@ohsu.edu
Shane T Hentges
Viviana F Bumaschny
Flavio S J de Souza
James L Smart
Andrea M Santangelo
Malcolm J Low
Gary L Westbrook
Marcelo Rubinstein
Vollum Institute · USCentro de Investigaciones Biológicas Margarita Salas · ESOregon Health & Science University · US

Funding

Neurochemistry/Physiology of Proopiomelanocortin NeuronsR01DK066604 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOW, MALCOLM JAMES · 2004 to 2019
$5.2M
POMC REGULATION OF HUMAN OBESITYP01DK055819 · NIDDK · OREGON HEALTH AND SCIENCE UNIVERSITY · PI CONE, ROGER D · 1999 to 2003
$4.4M
SYNAPTIC TRANSMISSION IN THE CNSR01NS026494 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI WESTBROOK, GARY L · 1993 to 2009
$3.0M
NEURAL SPECIFIC REGULATION OF PROOPIOMELANOCORTIN GENE ER03TW001233 · FIC · OREGON HEALTH AND SCIENCE UNIVERSITY · PI LOW, MALCOLM JAMES · 2000 to 2005
$239k
EXCITATORY SYNAPTIC MECHANISMS IN THE CNSR29NS026494 · NINDS · OREGON HEALTH AND SCIENCE UNIVERSITY · PI WESTBROOK, GARY L · 1988 to 1992
–
FIC NIH HHS R03 TW001233FIC NIH HHS TW01233NIDDK NIH HHS DK55819NIDDK NIH HHS P01 DK055819NIDDK NIH HHS R01 DK066604NINDS NIH HHS NS26494NINDS NIH HHS R01 NS026494
6 · The paper itself

Abstract

Neurogenesis in the dentate gyrus continues into adulthood, yet little is known about the function of newly born neurons or how they integrate into an existing network of mature neurons. We made transgenic mice that selectively and transiently express enhanced green fluorescent protein (EGFP) in newly born granule cells of the dentate gyrus under the transcriptional control of proopiomelanocortin (POMC) genomic sequences. Analysis of transgenic pedigrees with truncation or deletion mutations indicated that EGFP expression in the dentate gyrus required cryptic POMC promoter regions dispensable for arcuate hypothalamic or pituitary expression. Unlike arcuate neurons, dentate granule cells did not express the endogenous POMC gene. EGFP-positive neurons had immature properties, including short spineless dendrites and small action potentials. Colocalization with bromodeoxyuridine indicated that EGFP-labeled granule cells were approximately 2 weeks postmitotic. EGFP-labeled cells expressed markers for immature granule cells but not the glial marker GFAP. The number of EGFP-labeled neurons declined with age and increased with exercise, paralleling neurogenesis. Our results indicate that POMC-EGFP marks immature granule cells and that adult-generated granule cells integrate quite slowly into the hippocampal circuitry.

Indexed as

Action PotentialsAgingAnimalsBiomarkersBromodeoxyuridineCell CountCell DivisionCell MovementDentate GyrusGenes, ReporterGreen Fluorescent ProteinsLuminescent ProteinsMiceMice, Inbred C57BLMice, TransgenicNeural Cell Adhesion Molecule L1BiomarkersBromodeoxyuridineGreen Fluorescent ProteinsLuminescent ProteinsNeural Cell Adhesion Molecule L1polysialyl neural cell adhesion moleculePro-OpiomelanocortinSialic Acids

Identifiers

PMID15056704
PMCPMC6730035
OpenAlexW2151189924

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.