CPTCs Drive Somatic-Visceral Communication via the Wnt Axis in Somatic Mechanotherapy: A Single-Cell Deep Learning Study

Fuente: arXiv
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Autores principales: Huang, Haixiang, Zhang, Zhenwei, Shen, BingBing, Yue, Jianming, Mei, Lu, Zhu, Xudong, Shi, Yonghong, Zhu, Qianmei, Shi, Yeping, Luo, Yifan, Xing, Yitong, Dai, Meng, Chen, Qiusheng
Formato: Preprint
Publicado: 2026
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author Huang, Haixiang
Zhang, Zhenwei
Shen, BingBing
Yue, Jianming
Mei, Lu
Zhu, Xudong
Shi, Yonghong
Zhu, Qianmei
Shi, Yeping
Luo, Yifan
Xing, Yitong
Dai, Meng
Chen, Qiusheng
author_facet Huang, Haixiang
Zhang, Zhenwei
Shen, BingBing
Yue, Jianming
Mei, Lu
Zhu, Xudong
Shi, Yonghong
Zhu, Qianmei
Shi, Yeping
Luo, Yifan
Xing, Yitong
Dai, Meng
Chen, Qiusheng
contents Somatic mechanical stimulation (e.g., acupuncture) exerts systemic immunomodulatory effects, yet the cellular bridge translating peripheral physical force into visceral repair remains elusive. Here, employing a custom interpretable deep learning framework (CARSS) on single-cell RNA sequencing data, we identify CD34$^{+}$PDGFR$α$$^{+}$ telocytes (CPTCs) as the primary mechanosensors in both fascia and colon during bacterial colitis. We show that somatic mechanotherapy triggers an AP-1/Hsp70-dependent transcriptional program in fascial CPTCs, inducing systemic Wnt elevation, which elicits a "transcriptional resonance" in colonic CPTCs, reprogramming their communication network from an inflammatory amplifier to a Wnt-driven regenerative hub. Mechanistically, this axis activates epithelial $β$-catenin/Myc signaling, suppressing apoptosis and restoring barrier integrity independent of immune cells. Our findings define a CPTC-Driven Mechano-Resonance Axis, where CPTCs serve as synchronized relay stations that convert local mechanical cues into systemic regenerative microenvironments.
format Preprint
id arxiv_https___arxiv_org_abs_2602_05451
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle CPTCs Drive Somatic-Visceral Communication via the Wnt Axis in Somatic Mechanotherapy: A Single-Cell Deep Learning Study
Huang, Haixiang
Zhang, Zhenwei
Shen, BingBing
Yue, Jianming
Mei, Lu
Zhu, Xudong
Shi, Yonghong
Zhu, Qianmei
Shi, Yeping
Luo, Yifan
Xing, Yitong
Dai, Meng
Chen, Qiusheng
Biomolecules
Somatic mechanical stimulation (e.g., acupuncture) exerts systemic immunomodulatory effects, yet the cellular bridge translating peripheral physical force into visceral repair remains elusive. Here, employing a custom interpretable deep learning framework (CARSS) on single-cell RNA sequencing data, we identify CD34$^{+}$PDGFR$α$$^{+}$ telocytes (CPTCs) as the primary mechanosensors in both fascia and colon during bacterial colitis. We show that somatic mechanotherapy triggers an AP-1/Hsp70-dependent transcriptional program in fascial CPTCs, inducing systemic Wnt elevation, which elicits a "transcriptional resonance" in colonic CPTCs, reprogramming their communication network from an inflammatory amplifier to a Wnt-driven regenerative hub. Mechanistically, this axis activates epithelial $β$-catenin/Myc signaling, suppressing apoptosis and restoring barrier integrity independent of immune cells. Our findings define a CPTC-Driven Mechano-Resonance Axis, where CPTCs serve as synchronized relay stations that convert local mechanical cues into systemic regenerative microenvironments.
title CPTCs Drive Somatic-Visceral Communication via the Wnt Axis in Somatic Mechanotherapy: A Single-Cell Deep Learning Study
topic Biomolecules
url https://arxiv.org/abs/2602.05451