Ribonuclease 4 Functions in Nociceptor-Mediated Nerve Homeostasis

The regulation of nociceptor identity and function is essential, as disruptions can significantly influence pain sensation, yet our understanding of the molecular mechanisms involved remains incomplete. In this study, we identified ribonuclease 4 (RNase4) as selectively expressed in the unmyelinated nociceptor lineage. Analysis of RNase4-deficient mice and single-cell transcriptomic data revealed a cell-autonomous role for RNase4 in regulating nociceptor function. Moreover, in a neuropathic pain model, RNase4 expression was upregulated in nociceptors during the pain and recovery phases, and its deletion altered mechanical sensation. Additionally, RNase4 exerted non-cell- autonomous effects on the myelin structural organization of adjacent myelinated axons. Together, these findings implicate RNase4 as a dual regulator of nociceptor biology and myelin integrity, revealing a molecular pathway for pain regulation and nerve repair.

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Publication Details

Journal
Nature Communications
Published
2026-03-24
DOI
https://doi.org/10.1038/s41467-026-70365-8
Primary Topic
Pain Mechanisms and Treatments
Type
article
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article

Ribonuclease 4 Functions in Nociceptor-Mediated Nerve Homeostasis

Nature Communications
Pain Mechanisms and Treatments
article

Ribonuclease 4 Functions in Nociceptor-Mediated Nerve Homeostasis

article en

Abstract

The regulation of nociceptor identity and function is essential, as disruptions can significantly influence pain sensation, yet our understanding of the molecular mechanisms involved remains incomplete. In this study, we identified ribonuclease 4 (RNase4) as selectively expressed in the unmyelinated nociceptor lineage. Analysis of RNase4-deficient mice and single-cell transcriptomic data revealed a cell-autonomous role for RNase4 in regulating nociceptor function. Moreover, in a neuropathic pain model, RNase4 expression was upregulated in nociceptors during the pain and recovery phases, and its deletion altered mechanical sensation. Additionally, RNase4 exerted non-cell- autonomous effects on the myelin structural organization of adjacent myelinated axons. Together, these findings implicate RNase4 as a dual regulator of nociceptor biology and myelin integrity, revealing a molecular pathway for pain regulation and nerve repair.

Nature CommunicationsVol. 17(1)
Human Genome Sciences (United States) (US), Wenzhou Medical University (CN), First Affiliated Hospital of Wenzhou Medical University (CN), Karolinska Institutet (SE), Wenner-Gren Foundations (SE), University of Nebraska Medical Center (US)
Openalex Percentile: Top 10%
Pain Mechanisms and Treatments
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