Evidence map›Paper›PMID 35881440›Full record

ArticleeLife2022

Dopamine neuron morphology and output are differentially controlled by mTORC1 and mTORC2.

Polina Kosillo, Kamran M Ahmed, Erin E Aisenberg, Vasiliki Karalis, Bradley M Roberts, Stephanie J Cragg, Helen S Bateup

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  10. Restoration of locus coeruleus noradrenergic transmission during sleep.bioRxiv : the preprint server for biology · 2024
    Article
  11. Article
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  13. Review
  14. Article
  15. Transcriptional Dysregulation and Impaired Neuronal Activity inInternational journal of molecular sciences · 2023
    Article
  16. Review
  17. Article
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 3 institutions in 2 countries.

Polina Kosillo *Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.ORCID 0000-0002-1944-9460
Kamran M Ahmed *Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.ORCID 0000-0002-7204-5991
Erin E AisenbergHelen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, United States.
Vasiliki KaralisDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
Bradley M RobertsDepartment of Physiology, Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-5192-2545
Stephanie J CraggDepartment of Physiology, Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-9677-2256
Helen S BateupDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.ORCID 0000-0002-0135-0972
University of California, Berkeley · USUniversity of Oxford · GBChan Zuckerberg Initiative (United States) · US

Funding

Neuroscience Training Program at UC BerkeleyT32NS095939 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BATEUP, HELEN S. · 2016 to 2025
$6.3M
The impact of Tsc-mTOR signaling on basal ganglia functionR01NS105634 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BATEUP, HELEN S. · 2019 to 2022
$1.3M
Medical Research Council G0700932Medical Research Council MR/J004324/1Medical Research Council MR/K013866/1Medical Research Council MR/V013599/1NINDS NIH HHS R01 NS105634NINDS NIH HHS T32 NS095939Parkinson's UK G-0803Parkinson's UK G-0808Parkinson's UK G-1103Parkinson's UK G-1305Parkinson's UK H-1003Parkinson's UK J-0901
6 · The paper itself

Abstract

The mTOR pathway is an essential regulator of cell growth and metabolism. Midbrain dopamine neurons are particularly sensitive to mTOR signaling status as activation or inhibition of mTOR alters their morphology and physiology. mTOR exists in two distinct multiprotein complexes termed mTORC1 and mTORC2. How each of these complexes affect dopamine neuron properties, and whether they have similar or distinct functions is unknown. Here, we investigated this in mice with dopamine neuron-specific deletion of

Indexed as

DopamineDopaminergic NeuronsAnimalsMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2MiceTOR Serine-Threonine KinasesDopamineMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2TOR Serine-Threonine Kinasesdopamine neuronsmousemTORC1mTORC2neuroscienceraptorrictorTSC

Identifiers

PMID35881440
PMCPMC9328766
OpenAlexW4288035686

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.