Evidence map›Paper›PMID 42818675›Full record

ArticlebioRxiv : the preprint server for biology2026

Reversible, Sexually Dimorphic Sympathetic Aging: Distal Axon Withdrawal Shaped by Prepubertal Gonadal Influences.

Gabriella Rita Pangilinan, Sagar Patil, Francisco Mires, George Ye, Victoria Bogomilova, Lorraine Tilley, Tali Goldkorn, Cassandra J McGill, Nina Ballou, Xue Li and 3 more

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

13 authors.

Gabriella Rita PangilinanDepartment of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90033, USA.ORCID 0000-0003-2662-7883
Sagar PatilDepartment of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90033, USA.
Francisco MiresDepartment of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90033, USA.
George YeDepartment of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90033, USA.
Victoria BogomilovaDepartment of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90033, USA.
Lorraine TilleyDepartment of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90033, USA.
Tali GoldkornDepartment of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90033, USA.
Cassandra J McGillUSC Leonard Davis School of Gerontology, University of Southern California, Los Angeles, CA 90089, USA.
Nina BallouDepartment of Medicine, Department of Biomedical Sciences, and Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Cedars-Sinai Health Sciences University, Los Angeles, CA 90048, USA.
Xue LiDepartment of Medicine, Department of Biomedical Sciences, and Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Cedars-Sinai Health Sciences University, Los Angeles, CA 90048, USA.
Unmesh JadhavDepartment of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90033, USA.
Bérénice A BenayounUSC Leonard Davis School of Gerontology, University of Southern California, Los Angeles, CA 90089, USA.
Yulia ShwartzDepartment of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA 90033, USA.

Funding

The Role of the Y Chromosome in Bladder Tumor Development, Growth And ProgressionP01CA278732 · NCI · CEDARS-SINAI MEDICAL CENTER · PI Anil V Parwani · 2023 to 2026
$10.7M
USC Geroscience Training in the Biology of AgingT32AG052374 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Sean P CURRAN · 2016 to 2026
$5.3M
Sex Differences in Multi-omic and System-Specific AgingU54AG099000 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JENNIFER A AILSHIRE, EILEEN M CRIMMINS · 2026 to 2026
$3.0M
Sexual Dimorphism in Bladder CancerR01CA267108 · NCI · CEDARS-SINAI MEDICAL CENTER · PI Xue Sean Li · 2022 to 2026
$2.9M
Training in Developmental Biology, Stem Cells and RegenerationT32HD060549 · NICHD · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Gage D Crump · 2011 to 2026
$2.5M
Deciphering hormonal regulation of neutrophil biologyR01AG076433 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BENAYOUN, BERENICE ANATH · 2022 to 2025
$2.1M
17 alpha-estradiol as a potential protective therapeutic against development of Alzheimer's diseaseF31AG084279 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MCGILL, CASSANDRA JOAN · 2023 to 2024
$97k
NCI NIH HHS P01 CA278732NCI NIH HHS R01 CA267108NIA NIH HHS F31 AG084279NIA NIH HHS R01 AG076433NIA NIH HHS T32 AG052374NIA NIH HHS U54 AG099000NICHD NIH HHS T32 HD060549
6 · The paper itself

Abstract

Peripheral innervation declines with age, but whether this process is sexually dimorphic and whether it reflects neuronal degeneration or deterioration of nerve-target interactions remain unclear. Using mouse skin as a defined neuroeffector system, we show that sympathetic aging is strongly sexually dimorphic, with greater denervation in aged males. Skin-projecting sympathetic neurons remain intact, indicating that denervation reflects distal axon withdrawal rather than neuronal loss. Nerve-target interactions and the arrector pili muscle niche deteriorate with age, predominantly in males. Aged sympathetic neurons retain NGF responsiveness, and restoring NGF within arrector pili muscles promotes sympathetic reinnervation and hair regeneration in aged males. Genetic and endocrine models show that divergent aging trajectories are associated with gonadal rather than chromosomal sex and are attenuated by early gonadectomy. Together, these findings identify sympathetic aging as a reversible, sexually dimorphic distal axonopathy shaped by the target environment and gonadal influences.

Indexed as

agingarrector pili musclehair follicle stem cellsnerve growth factor (NGF)neuroeffector nicheneurotrophic signalingperipheral innervationperipheral neuropathySex differencesSympathetic nervous systemtissue regeneration

Identifiers

PMID42818675
PMCPMC13622557

What OpenQuestion holds

Textmetadata
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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.