Evidence map›Paper›PMID 42465371›Full record

ArticlebioRxiv : the preprint server for biology2026

Spatial confinement shapes organelle architecture and remodeling in axons.

Mihir Relan, Venkata Mallampalli, Benjamin A Barad, Andrea K H Stavoe, M Neal Waxham

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

5 authors.

Mihir RelanDepartment of Neurobiology and Anatomy, University of Texas Health Science Center at Houston, Houston, TX 77030.ORCID 0000-0003-0100-6589
Venkata MallampalliDepartment of Neurobiology and Anatomy, University of Texas Health Science Center at Houston, Houston, TX 77030.ORCID 0009-0004-2006-1721
Benjamin A BaradDepartment of Chemical Physiology and Biochemistry, School of Medicine, Oregon Health & Science University, Portland, OR, USA.ORCID 0000-0002-1016-862X
Andrea K H StavoeDepartment of Neurobiology and Anatomy, University of Texas Health Science Center at Houston, Houston, TX 77030.ORCID 0000-0002-4073-4565
M Neal WaxhamDepartment of Neurobiology and Anatomy, University of Texas Health Science Center at Houston, Houston, TX 77030.ORCID 0000-0003-4801-1190

Funding

ACQUISITION OF HIGH-THROUGHPUT 200 kV CRYO-TEMS10OD032204 · OD · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI SERYSHEVA, IRINA I · 2022 to 2022
$2.0M
Ultrastructural alterations to neuronal autophagy during aging delineated with Cryo-EM tomographyR21AG090967 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI STAVOE, ANDREA · 2025 to 2025
$429k
NIA NIH HHS R21 AG090967NIH HHS S10 OD032204
6 · The paper itself

Abstract

Axons are extended cellular compartments that mediate neuronal connectivity over extraordinary distances, placing unique demands on local organelle organization and trafficking. How these geometric constraints influence organelle architecture remains poorly understood. Here, we used cryo-electron tomography and quantitative morphometric analyses to define the three-dimensional ultrastructural organization of dorsal root ganglion axons in a near-native state. We identify distinct vesicle populations with tightly versus broadly constrained size distributions and reveal a continuum of endolysosomal and autophagic intermediates that highlight the dynamic nature of membrane remodeling in growing axons. Unexpectedly, we observe vesicular structures enclosed within the lumen of the endoplasmic reticulum, suggesting a previously undescribed mechanism of ER membrane remodeling. Across multiple organelle classes, morphology and size are constrained by axonal geometry. This principle is most evident in mitochondria, which undergo dramatic narrowing and remodeling at varicosity-axon boundaries to traverse confined axonal segments. Together, these findings reveal spatial confinement as a fundamental organizing principle of axonal cell biology.

Indexed as

axonal cytoskeletonCryo-electron tomographydorsal root ganglionneural networksorganelle remodelingspatial confinement

Identifiers

PMID42465371
PMCPMC13370410

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.