Evidence map›Paper›PMID 37788670›Full record

ArticleNeuron2023

Neuronal activity drives IGF2 expression from pericytes to form long-term memory.

Kiran Pandey, Benjamin Bessières, Susan L Sheng, Julian Taranda, Pavel Osten, Ionel Sandovici, Miguel Constancia, Cristina M Alberini

Open access · bronzeAbstract read
In one paragraph

Article in Neuron, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.0field-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

20 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Eppur si muove: the dynamic brain pericyte.Fluids and barriers of the CNS · 2025
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Kiran PandeyCenter for Neural Science, New York University, New York, NY 10003, USA.
Benjamin BessièresCenter for Neural Science, New York University, New York, NY 10003, USA.
Susan L ShengCenter for Neural Science, New York University, New York, NY 10003, USA.
Julian TarandaCold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
Pavel OstenCold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
Ionel SandoviciUniversity of Cambridge Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Institute of Metabolic Science, Addenbrookes Hospital, Cambridge, UK; Department of Obstetrics and Gynaecology and National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, UK; Centre for Trophoblast Research, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Miguel ConstanciaUniversity of Cambridge Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Institute of Metabolic Science, Addenbrookes Hospital, Cambridge, UK; Department of Obstetrics and Gynaecology and National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, UK; Centre for Trophoblast Research, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Cristina M AlberiniCenter for Neural Science, New York University, New York, NY 10003, USA. Electronic address: ca60@nyu.edu.
New York University · USCold Spring Harbor Laboratory · USUniversity of Cambridge · GB

Funding

Gene Expression in Long-Term MemoryR01MH065635 · NIMH · NEW YORK UNIVERSITY · PI CRISTINA M ALBERINI · 2002 to 2026
$7.5M
Gene Expression in Long-Term MemoryR37MH065635 · NIMH · NEW YORK UNIVERSITY · PI ALBERINI, CRISTINA M · 2013 to 2022
$5.6M
Medical Research Council MC_UU_00014/4NIMH NIH HHS R01 MH065635NIMH NIH HHS R37 MH065635
6 · The paper itself

Abstract

Investigations of memory mechanisms have been, thus far, neuron centric, despite the brain comprising diverse cell types. Using rats and mice, we assessed the cell-type-specific contribution of hippocampal insulin-like growth factor 2 (IGF2), a polypeptide regulated by learning and required for long-term memory formation. The highest level of hippocampal IGF2 was detected in pericytes, the multi-functional mural cells of the microvessels that regulate blood flow, vessel formation, the blood-brain barrier, and immune cell entry into the central nervous system. Learning significantly increased pericytic Igf2 expression in the hippocampus, particularly in the highly vascularized stratum lacunosum moleculare and stratum moleculare layers of the dentate gyrus. Igf2 increases required neuronal activity. Regulated hippocampal Igf2 knockout in pericytes, but not in fibroblasts or neurons, impaired long-term memories and blunted the learning-dependent increase of neuronal immediate early genes (IEGs). Thus, neuronal activity-driven signaling from pericytes to neurons via IGF2 is essential for long-term memory.

Indexed as

NeuronsPericytesAnimalsHippocampusInsulin-Like Growth Factor IIMemory, Long-TermMiceRatsRNA-Binding ProteinsSignal TransductionIgf2bp1 protein, ratIGF2 protein, mouseInsulin-Like Growth Factor IIRNA-Binding Proteinsfibroblasthippocampusimmediate early geneinsulin-like growth factor 2long-term memorymouseneuronneuronal activitypericyterat

Identifiers

PMID37788670
PMCPMC10843759
OpenAlexW4387253054

What OpenQuestion holds

Textmetadata
LicenceTDM
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.