Evidence map›Paper›PMID 17013619›Full record

ArticleExperimental brain research2007

Time of transplantation and cell preparation determine neural stem cell survival in a mouse model of Huntington's disease.

Verena Johann, Johannes Schiefer, Christian Sass, Jörg Mey, Gary Brook, Alexander Krüttgen, Christiane Schlangen, Christian Bernreuther, Melitta Schachner, Marcel Dihné and 1 more

Abstract read
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Article in Experimental brain research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.2field-weighted citation impact, top 26% 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

24 citing papers in PubMed, 70 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Verena JohannDepartment of Neurology, University Hospital RWTH, Pauwelsstr. 30, 52074 Aachen, Germany.
Johannes Schiefer
Christian Sass
Jörg Mey
Gary Brook
Alexander Krüttgen
Christiane Schlangen
Christian Bernreuther
Melitta Schachner
Marcel Dihné
Christoph M Kosinski
RWTH Aachen University · DEUniversität Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell replacement therapies for neurodegenerative diseases, using multipotent neural stem cells (NSCs), require above all, a good survival of the graft. In this study, we unilaterally injected quinolinic acid (QA) into the striatum of adult mice and transplanted syngeneic NSCs of enhanced green fluorescent protein-transgenic mice into the lesioned striatum. The injection of QA leads to an excitotoxic lesion with selective cell death of the medium sized spiny neurons, the same cells that are affected in Huntington's disease. In order to investigate the best timing of transplantation for the survival of donor cells, we transplanted the stem cells at 2, 7 and 14 days after injury. In addition, the influence of graft preparation prior to transplantation, i.e., intact neurospheres versus dissociated cell suspension on graft survival was investigated. By far the best survival was found with the combination of early transplantation (i.e., 2 days after QA-lesion) with the use of neurospheres instead of dissociated cell suspension. This might be due to the different states of host's astrocytic and microglia activation which we found to be moderate at 2, but pronounced at 7 and 14 days after QA-lesion. We also investigated brain derived neurotrophic factor (BDNF)-expression in the striatum after QA-lesion and found no significant change in BDNF protein-level. We conclude that already the method of graft preparation of NSCs for transplantation, as well as the timing of the transplantation procedure strongly affects the survival of the donor cells when grafted into the QA-lesioned striatum of adult mice.

Indexed as

AnimalsBrain-Derived Neurotrophic FactorBrain Tissue TransplantationCell Culture TechniquesCells, CulturedCell SurvivalCorpus StriatumDenervationDisease Models, AnimalFemaleGliosisGraft SurvivalGreen Fluorescent ProteinsHuntington DiseaseMaleMiceBrain-Derived Neurotrophic Factorenhanced green fluorescent proteinGreen Fluorescent ProteinsNeurotoxins

Identifiers

PMID17013619
OpenAlexW2069465086

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.