Evidence map›Paper›PMID 36107951›Full record

ArticlePloS one2022

Protracted neuronal maturation in a long-lived, highly social rodent.

Mariela Faykoo-Martinez, Troy Collins, Diana Peragine, Manahil Malik, Fiza Javed, Matthew Kolisnyk, Justine Ziolkowski, Imaan Jeewa, Arthur H Cheng, Christopher Lowden and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Dynamic expression of lamin B1 during adult neurogenesis in the vertebrate brain.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
    Article
  2. Review
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

13 authors at 1 institution in 1 country.

Mariela Faykoo-MartinezDepartment of Cell and Systems Biology, University of Toronto, Toronto, ON, Canada.ORCID 0000-0002-8885-657X
Troy CollinsDepartment of Cell and Systems Biology, University of Toronto, Toronto, ON, Canada.
Diana PeragineDepartment of Psychology, University of Toronto Mississauga, Mississauga, ON, Canada.
Manahil MalikDepartment of Psychology, University of Toronto Mississauga, Mississauga, ON, Canada.
Fiza JavedDepartment of Psychology, University of Toronto Mississauga, Mississauga, ON, Canada.
Matthew KolisnykDepartment of Psychology, University of Toronto Mississauga, Mississauga, ON, Canada.
Justine ZiolkowskiDepartment of Psychology, University of Toronto Mississauga, Mississauga, ON, Canada.
Imaan JeewaDepartment of Psychology, University of Toronto Mississauga, Mississauga, ON, Canada.
Arthur H ChengDepartment of Cell and Systems Biology, University of Toronto, Toronto, ON, Canada.
Christopher LowdenDepartment of Cell and Systems Biology, University of Toronto, Toronto, ON, Canada.
Brittany MascarenhasDepartment of Cell and Systems Biology, University of Toronto, Toronto, ON, Canada.
Hai-Ying Mary ChengDepartment of Cell and Systems Biology, University of Toronto, Toronto, ON, Canada.ORCID 0000-0002-9292-7406
Melissa M HolmesDepartment of Cell and Systems Biology, University of Toronto, Toronto, ON, Canada.
University of Toronto · CA

Funding

CIHR 02003PJT-437197
6 · The paper itself

Abstract

Naked mole-rats are a long-lived rodent species (current lifespan >37 years) and an increasingly popular biomedical model. Naked mole-rats exhibit neuroplasticity across their long lifespan. Previous studies have begun to investigate their neurogenic patterns. Here, we test the hypothesis that neuronal maturation is extended in this long-lived rodent. We characterize cell proliferation and neuronal maturation in established rodent neurogenic regions over 12 months following seven days of consecutive BrdU injection. Given that naked mole-rats are eusocial (high reproductive skew where only a few socially-dominant individuals reproduce), we also looked at proliferation in brain regions relevant to the social-decision making network. Finally, we measured co-expression of EdU (newly-born cells), DCX (immature neuron marker), and NeuN (mature neuron marker) to assess the timeline of neuronal maturation in adult naked mole-rats. This work reaffirms the subventricular zone as the main source of adult cell proliferation and suggests conservation of the rostral migratory stream in this species. Our profiling of socially-relevant brain regions suggests that future work which manipulates environmental context can unveil how newly-born cells integrate into circuitry and facilitate adult neuroplasticity. We also find naked mole-rat neuronal maturation sits at the intersection of rodents and long-lived, non-rodent species: while neurons can mature by 3 weeks (rodent-like), most neurons mature at 5 months and hippocampal neurogenic levels are low (like long-lived species). These data establish a timeline for future investigations of longevity- and socially-related manipulations of naked mole-rat adult neurogenesis.

Indexed as

Mole RatsNeurogenesisAnimalsBromodeoxyuridineLongevityNeuronsBromodeoxyuridine

Identifiers

PMID36107951
PMCPMC9477366
OpenAlexW4295900657

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.