Evidence map›Paper›PMID 42818440›Full record

ArticlebioRxiv : the preprint server for biology2026

Parenchymal precursor cells act in concert with canonical neural progenitors to facilitate neural circuit recovery following neuronal loss.

William C Tucker, Susanna L Shepard, Paige E Chambers, Anya Majji, John M Boyd, Tracy A Larson

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

William C TuckerDepartment of Biology, University of Virginia, Charlottesville, Virginia, USA, 22903.
Susanna L ShepardDepartment of Biology, University of Virginia, Charlottesville, Virginia, USA, 22903.
Paige E ChambersDepartment of Biology, University of Virginia, Charlottesville, Virginia, USA, 22903.
Anya MajjiDepartment of Biology, University of Virginia, Charlottesville, Virginia, USA, 22903.
John M BoydDepartment of Biology, University of Virginia, Charlottesville, Virginia, USA, 22903.
Tracy A LarsonDepartment of Biology, University of Virginia, Charlottesville, Virginia, USA, 22903.

Funding

Mechanisms of cyclical degeneration and regeneration in an avian model systemR35GM150562 · NIGMS · UNIVERSITY OF VIRGINIA · PI TRACY ALISON LARSON · 2023 to 2026
$1.8M
NIGMS NIH HHS R35 GM150562
6 · The paper itself

Abstract

Seasonal environmental variation represents one of the most pervasive and recurring forces shaping the vertebrate brain through cycles of neural circuit plasticity and remodeling that ultimately serves to maintain adaptive behavior. Although the contribution of adult neurogenesis to such remodeling is well-characterized across vertebrates, the role of astrocytes in supporting or enabling this process remains almost entirely unknown. Here, using the robust and natural seasonal loss of neurons within the sensorimotor nucleus HVC of the songbird, we identify a rapid astrocytic turnover event following neuronal loss and reveal a previously undescribed cellular mechanism supporting neural circuit recovery. Using lineage-specific and proliferation labeling, we establish the presence of a previously undescribed SOX2-positive neural progenitor-like population residing within the vertebrate parenchyma, outside the canonical ventricular zone niche. These parenchymal astrocyte precursor cells (pAPCs) maintain quantifiable, steady-state proliferation under homeostatic conditions, yet expand in pool size following seasonally-driven neuronal loss. The coordinated response of canonical neural progenitor cells and pAPCs produces new astrocytes that persist throughout the re-establishment of homeostasis. These findings reveal extensive astrocyte plasticity in the adult vertebrate brain, operating across both canonical and non-canonical progenitor niches, and challenge the prevailing view that parenchymal astrocytes are largely post-mitotic outside of injury contexts. More broadly, our findings establish a framework for understanding how glial populations contribute to neural circuit resilience both to the physiological and neural changes that recurring seasonal transitions drive, and to the accelerating environmental changes that increasingly challenge the adaptive capacity of animal brains worldwide.

Indexed as

Astrocytebehavioral plasticitybirdsongcircuit remodelingenvironmental neurobiologyneuronal deathnon-canonical nichereactive proliferationseasonal plasticity

Identifiers

PMID42818440
PMCPMC13622398

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.