Evidence map›Paper›PMID 22649242›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

Critical time window of neuronal cholesterol synthesis during neurite outgrowth.

Ursula Fünfschilling, Wolf J Jockusch, Nandhini Sivakumar, Wiebke Möbius, Kristina Corthals, Sai Li, Susanne Quintes, Younghoon Kim, Iwan A T Schaap, Jeong-Seop Rhee and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

51 citing papers in PubMed, 85 citations in OpenAlex.

  1. Beneficially Stressing the Peripheral Nervous System to Repair.International journal of molecular sciences · 2026
    Review
  2. Sterol biosynthesis, brain development, and disease.The Journal of clinical investigation · 2026
    Review
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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

12 authors at 5 institutions in 2 countries.

Ursula FünfschillingDepartment of Neurogenetics, Max Planck Institute for Experimental Medicine, 37075 Göttingen, Germany.
Wolf J Jockusch
Nandhini Sivakumar
Wiebke Möbius
Kristina Corthals
Sai Li
Susanne Quintes
Younghoon Kim
Iwan A T Schaap
Jeong-Seop Rhee
Klaus-Armin Nave
Gesine Saher
Max Planck Society · DEMax Planck Institute of Experimental Medicine · DEMax Planck Research Unit for Neurogenetics · DEUniversity of Göttingen · DEKyung Hee University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholesterol is an essential membrane component enriched in plasma membranes, growth cones, and synapses. The brain normally synthesizes all cholesterol locally, but the contribution of individual cell types to brain cholesterol metabolism is unknown. To investigate whether cortical projection neurons in vivo essentially require cholesterol biosynthesis and which cell types support neurons, we have conditionally ablated the cholesterol biosynthesis in these neurons in mice either embryonically or postnatally. We found that cortical projection neurons synthesize cholesterol during their entire lifetime. At all stages, they can also benefit from glial support. Adult neurons that lack cholesterol biosynthesis are mainly supported by astrocytes such that their functional integrity is preserved. In contrast, microglial cells support young neurons. However, compensatory efforts of microglia are only transient leading to layer-specific neuronal death and the reduction of cortical projections. Hence, during the phase of maximal membrane growth and maximal cholesterol demand, neuronal cholesterol biosynthesis is indispensable. Analysis of primary neurons revealed that neurons tolerate only slight alteration in the cholesterol content and plasma membrane tension. This quality control allows neurons to differentiate normally and adjusts the extent of neurite outgrowth, the number of functional growth cones and synapses to the available cholesterol. This study highlights both the flexibility and the limits of horizontal cholesterol transfer in vivo and may have implications for the understanding of neurodegenerative diseases.

Indexed as

Analysis of VarianceAnimalsAnimals, NewbornAnticholesteremic AgentsApolipoproteins EBacterial ProteinsBasic Helix-Loop-Helix Proteinsbeta-CyclodextrinsBridged Bicyclo Compounds, HeterocyclicCalcium-Calmodulin-Dependent Protein Kinase Type 2Cell DifferentiationCells, CulturedCell SurvivalCerebral CortexCholesterolEmbryo, MammalianAnticholesteremic AgentsApolipoproteins EBacterial ProteinsBasic Helix-Loop-Helix Proteinsbeta-CyclodextrinsBridged Bicyclo Compounds, HeterocyclicCalcium-Calmodulin-Dependent Protein Kinase Type 2CholesterolEphrin-A5Farnesyl-Diphosphate FarnesyltransferaseGlial Fibrillary Acidic ProteinLuminescent Proteinsmethyl-beta-cyclodextrinNerve Tissue ProteinsNeurod6 protein, mouseRNA, Messengersqualestatin 1Tricarboxylic Acidsyellow fluorescent protein, Bacteria

Identifiers

PMID22649242
PMCPMC6703588
OpenAlexW1986228536

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.