Evidence map›Paper›PMID 31488328›Full record

ArticleNeuron2019

Inducing Different Neuronal Subtypes from Astrocytes in the Injured Mouse Cerebral Cortex.

Nicola Mattugini, Riccardo Bocchi, Volker Scheuss, Gianluca Luigi Russo, Olof Torper, Chu Lan Lao, Magdalena Götz

Open access · hybridAbstract read
In one paragraph

Article in Neuron, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
9.0field-weighted citation impact, top 1% 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

98 citing papers in PubMed, 166 citations in OpenAlex.

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  7. Astrocyte Enrichment of 3D Cortical Constructs Enhances Brain Repair.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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38 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

7 authors at 2 institutions in 1 country.

Nicola MattuginiPhysiological Genomics, Biomedical Center (BMC), Ludwig-Maximilians-Universitaet (LMU), Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany; Helmholtz Center Munich, Biomedical Center (BMC), Institute of Stem Cell Research, Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany; Graduate School of Systemic Neuroscience, Ludwig-Maximilians-Universitaet (LMU), Großhaderner Str. 2, 82152 Planegg/Martinsried, Germany.
Riccardo BocchiPhysiological Genomics, Biomedical Center (BMC), Ludwig-Maximilians-Universitaet (LMU), Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany; Helmholtz Center Munich, Biomedical Center (BMC), Institute of Stem Cell Research, Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany.
Volker ScheussPhysiological Genomics, Biomedical Center (BMC), Ludwig-Maximilians-Universitaet (LMU), Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany; Helmholtz Center Munich, Biomedical Center (BMC), Institute of Stem Cell Research, Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany.
Gianluca Luigi RussoPhysiological Genomics, Biomedical Center (BMC), Ludwig-Maximilians-Universitaet (LMU), Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany; Helmholtz Center Munich, Biomedical Center (BMC), Institute of Stem Cell Research, Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany; Graduate School of Systemic Neuroscience, Ludwig-Maximilians-Universitaet (LMU), Großhaderner Str. 2, 82152 Planegg/Martinsried, Germany.
Olof TorperPhysiological Genomics, Biomedical Center (BMC), Ludwig-Maximilians-Universitaet (LMU), Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany; Helmholtz Center Munich, Biomedical Center (BMC), Institute of Stem Cell Research, Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany.
Chu Lan LaoPhysiological Genomics, Biomedical Center (BMC), Ludwig-Maximilians-Universitaet (LMU), Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany; Helmholtz Center Munich, Biomedical Center (BMC), Institute of Stem Cell Research, Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany.
Magdalena GötzPhysiological Genomics, Biomedical Center (BMC), Ludwig-Maximilians-Universitaet (LMU), Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany; Helmholtz Center Munich, Biomedical Center (BMC), Institute of Stem Cell Research, Großhaderner Str. 9, 82152 Planegg/Martinsried, Germany; SyNergy Excellence Cluster, Munich, Germany. Electronic address: magdalena.goetz@helmholtz-muenchen.de.
Helmholtz Zentrum München · DELudwig-Maximilians-Universität München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Astrocytes are particularly promising candidates for reprogramming into neurons, as they maintain some of the original patterning information from their radial glial ancestors. However, to which extent the position of astrocytes influences the fate of reprogrammed neurons remains unknown. To elucidate this, we performed stab wound injury covering an entire neocortical column, including the gray matter (GM) and white matter (WM), and targeted local reactive astrocytes via injecting FLEx switch (Cre-On) adeno-associated viral (AAV) vectors into mGFAP-Cre mice. Single proneural factors were not sufficient for adequate reprogramming, although their combination with the nuclear receptor-related 1 protein (Nurr1) improved reprogramming efficiency. Nurr1 and Neurogenin 2 (Ngn2) resulted in high-efficiency reprogramming of targeted astrocytes into neurons that develop lamina-specific hallmarks, including the appropriate long-distance axonal projections. Surprisingly, in the WM, we did not observe any reprogrammed neurons, thereby unveiling a crucial role of region- and layer-specific differences in astrocyte reprogramming.

Indexed as

AnimalsAstrocytesBasic Helix-Loop-Helix ProteinsBrain Injuries, TraumaticCellular Reprogramming TechniquesCerebral CortexDependovirusGenetic VectorsGliosisGray MatterMiceNerve Tissue ProteinsNeuronsNuclear Receptor Subfamily 4, Group A, Member 2Pyramidal CellsWhite MatterBasic Helix-Loop-Helix ProteinsNerve Tissue ProteinsNeurog2 protein, mouseNr4a2 protein, mouseNuclear Receptor Subfamily 4, Group A, Member 2AAVastrocytesaxonal projectioncerebral cortexcortical layerselectrophysiologyinflammationlentivirusreactive gliosisreprogramming

Identifiers

PMID31488328
PMCPMC6859713
OpenAlexW2971841027

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.