Researchers were surprised to find that inflammation in neighboring cells appears to keep neck nerves in a pain-sensitive state.

A new study found chronic neck pain may be driven by an inflammatory environment around the nerves.
Chronic neck pain is common and a leading cause of disability. Development of effective treatments has been limited by a lack of understanding of which biological pathways help generate and amplify painful signals in the neck.
In a molecular study of nerve cells in the upper necks of human patients, researchers were able to link pain with the activity of single cells.
“By linking human tissue to patients’ pain experiences, we hope to develop treatments that address the cause of persistent neck pain and ultimately improve patients’ quality of life,” said one of the paper’s authors, Dr. Michele Curatolo, professor of anesthesiology and pain medicine at the University of Washington School of Medicine. He directs the UW Medicine Interventional Pain Program.
The findings appeared in the April issue of the journal Brain.
Pain signals from the neck travel through small bundles of nerve cells called dorsal root ganglia, located just outside the spinal cord. The ganglia at the second cervical vertebra carries signals not only from the neck but also from the back of the head.
During certain spine surgeries, this upper-spine bundle is sometimes removed as part of routine care. The researchers were able to examine this tissue from 22 spine-surgery patients at UW Medicine to better understand the changes that occur in the cells when pain becomes chronic.
Half of the patients had recent, short-term neck pain, and half had chronic neck pain lasting three months or longer.
Using RNA sequencing, the researchers measured which genes were active in individual cells, located those cells within the dorsal root ganglia, and compared patterns between patients with acute versus chronic pain.
The researchers expected to see major changes in the ganglia’s nerve cells, or neurons, that transmit pain signals. They were surprised to find that the differences between acute and chronic neck pain were not in the nerve cells themselves.
Instead, major changes were seen in the cells surrounding and interacting with the nerve cells, including endothelial cells, which line the blood vessels, fibroblasts, which organize and support tissue, and Schwann cells, which insulate nerve fibers.
In patients with chronic neck pain, these non-neural cells showed strong, ongoing inflammation. Many of the more active genes were linked to inflammation, immune signaling, and pain sensitivity.
This suggests that non-neural cells may send chemical signals to nearby nerve cells, thereby keeping them in a painsensitive state. Consequently, chronic neck pain may be driven by an inflammatory environment around the nerves.
Source – UW Medicine
Researchers were surprised to find that inflammation in neighboring cells appears to keep neck nerves in a pain-sensitive state.
A new study found chronic neck pain may be driven by an inflammatory environment around the nerves.
Chronic neck pain is common and a leading cause of disability. Development of effective treatments has been limited by a lack of understanding of which biological pathways help generate and amplify painful signals in the neck.
In a molecular study of nerve cells in the upper necks of human patients, researchers were able to link pain with the activity of single cells.
The findings appeared in the April issue of the journal Brain.
Pain signals from the neck travel through small bundles of nerve cells called dorsal root ganglia, located just outside the spinal cord. The ganglia at the second cervical vertebra carries signals not only from the neck but also from the back of the head.
During certain spine surgeries, this upper-spine bundle is sometimes removed as part of routine care. The researchers were able to examine this tissue from 22 spine-surgery patients at UW Medicine to better understand the changes that occur in the cells when pain becomes chronic.
Half of the patients had recent, short-term neck pain, and half had chronic neck pain lasting three months or longer.
Using RNA sequencing, the researchers measured which genes were active in individual cells, located those cells within the dorsal root ganglia, and compared patterns between patients with acute versus chronic pain.
The researchers expected to see major changes in the ganglia’s nerve cells, or neurons, that transmit pain signals. They were surprised to find that the differences between acute and chronic neck pain were not in the nerve cells themselves.
Instead, major changes were seen in the cells surrounding and interacting with the nerve cells, including endothelial cells, which line the blood vessels, fibroblasts, which organize and support tissue, and Schwann cells, which insulate nerve fibers.
In patients with chronic neck pain, these non-neural cells showed strong, ongoing inflammation. Many of the more active genes were linked to inflammation, immune signaling, and pain sensitivity.
This suggests that non-neural cells may send chemical signals to nearby nerve cells, thereby keeping them in a painsensitive state. Consequently, chronic neck pain may be driven by an inflammatory environment around the nerves.
Source – UW Medicine
Arendt-Tranholm A, Sankaranarayanan I, Payne C, Mancilla Moreno M, Mazhar K, Yap N, Chiu A, Barry A, Patel P, Inturi N, Tavares-Ferreira D, Amin A, Karandikar M, Jarvik J, Turner J, Hofstetter C, Curatolo M, Price T. (2026) Transcriptome of the human C2 dorsal root ganglia in C1-2 arthrodesis surgery: insight for neck pain. Brain 149(4): 1349-1364. [article]
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Researchers were surprised to find that inflammation in neighboring cells appears to keep neck nerves in a pain-sensitive state.
A new study found chronic neck pain may be driven by an inflammatory environment around the nerves.
Chronic neck pain is common and a leading cause of disability. Development of effective treatments has been limited by a lack of understanding of which biological pathways help generate and amplify painful signals in the neck.
In a molecular study of nerve cells in the upper necks of human patients, researchers were able to link pain with the activity of single cells.
The findings appeared in the April issue of the journal Brain.
Pain signals from the neck travel through small bundles of nerve cells called dorsal root ganglia, located just outside the spinal cord. The ganglia at the second cervical vertebra carries signals not only from the neck but also from the back of the head.
During certain spine surgeries, this upper-spine bundle is sometimes removed as part of routine care. The researchers were able to examine this tissue from 22 spine-surgery patients at UW Medicine to better understand the changes that occur in the cells when pain becomes chronic.
Half of the patients had recent, short-term neck pain, and half had chronic neck pain lasting three months or longer.
Using RNA sequencing, the researchers measured which genes were active in individual cells, located those cells within the dorsal root ganglia, and compared patterns between patients with acute versus chronic pain.
The researchers expected to see major changes in the ganglia’s nerve cells, or neurons, that transmit pain signals. They were surprised to find that the differences between acute and chronic neck pain were not in the nerve cells themselves.
Instead, major changes were seen in the cells surrounding and interacting with the nerve cells, including endothelial cells, which line the blood vessels, fibroblasts, which organize and support tissue, and Schwann cells, which insulate nerve fibers.
In patients with chronic neck pain, these non-neural cells showed strong, ongoing inflammation. Many of the more active genes were linked to inflammation, immune signaling, and pain sensitivity.
This suggests that non-neural cells may send chemical signals to nearby nerve cells, thereby keeping them in a painsensitive state. Consequently, chronic neck pain may be driven by an inflammatory environment around the nerves.
Source – UW Medicine
Arendt-Tranholm A, Sankaranarayanan I, Payne C, Mancilla Moreno M, Mazhar K, Yap N, Chiu A, Barry A, Patel P, Inturi N, Tavares-Ferreira D, Amin A, Karandikar M, Jarvik J, Turner J, Hofstetter C, Curatolo M, Price T. (2026) Transcriptome of the human C2 dorsal root ganglia in C1-2 arthrodesis surgery: insight for neck pain. Brain 149(4): 1349-1364. [article]
Related Posts
Novel biosensor uses DNA ‘barcodes’ to uncover disease signals in cells
CellART extracts single-cell information from high-resolution spatial transcriptomics
Cell2space restores spatial context to single-cell RNA sequencing data
Urine test may improve bladder cancer diagnosis and guide treatment decisions
DeCoRE – a computational method to resolve RNA structural heterogeneity from RNA structure probing data by direct RNA sequencing
Tracing 700 million years of cell evolution
How should biological replicates be handled in long-read RNA sequencing?
RNA-Seq reveals a new way the developing heart controls its growth
The Human RNome Project Consortium seeks to publish first-ever complete sequence of the body’s RNA
scFlowReport brings multiple single-cell RNA sequencing analyses into one workflow
Long-read RNA sequencing reveals how neurons choose alternative RNA endings
DeOPUS improves cell-type estimates from bulk RNA sequencing
ResolVI improves accuracy in spatial transcriptomics analysis
RNA sequencing reveals transcriptional allele differences in prostate cancer stem cells
Unmasking “zombie cells” in aging tissue with an AI-powered barcode
RNA variant imaging for cancer diagnosis
Autism-risk mutations reveal two opposing patterns of brain gene activity
A real-data approach to evaluating RNA transcript analysis methods
Detection and sequencing of Ap2N-capped RNAs in human cells
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