{"title":"Ptgs2+ CPTC作为“力-免疫轴”响应针刺和介导M2巨噬细胞活化抗炎作用","authors":"Zhenwei Zhang, Haixiang Huang, Jianming Yue, Xudong Zhu, Yeping Shi, Bingbing Shen, Qianmei Zhu, Lu Mei, Qiusheng Chen","doi":"10.1096/fj.202501175RR","DOIUrl":null,"url":null,"abstract":"<p>Recent advancements have highlighted the imperative for cytological exploration of fascial tissues. Telocytes, specialized interstitial cells found in connective tissues such as fascia, have garnered significant attention. Our study explored the cellular landscape of the abdominal midline fascia (AMF), revealing a primary presence of Cd34+/Pdgfra+ telocytes (CPTCs) by single-cell sequencing and cytomorphology. We identified six CPTC subpopulations with deep learning, notably Ptgs2+ CPTCs, which exhibited remarkable responsiveness to mechanical stimulus. Following the acupuncture stimulation at the special acupoints along the AMF in dysenteric rats, the proportion of Ptgs2+ CPTCs increased significantly, with these cells exhibiting strengthened cell adhesion with all CPTC subpopulations. Importantly, Ptgs2+ CPTCs activated M2 macrophages through the Il6–Il6st–Stat3 pathway, promoting anti-inflammatory responses. For the first time, our findings established Ptgs2+ CPTCs as a key “force–immune axis” that linked mechanical stimulation and immune modulation, advancing our understanding of the cellular mechanisms behind acupuncture and its potential to modulate inflammation in immune-related disorders.</p>","PeriodicalId":50455,"journal":{"name":"The FASEB Journal","volume":"39 19","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12477662/pdf/","citationCount":"0","resultStr":"{\"title\":\"Ptgs2+ CPTC Function as a “Force-Immune Axis” by Responding to Acupuncture and Mediating M2 Macrophage Activation for Anti-Inflammatory Effects\",\"authors\":\"Zhenwei Zhang, Haixiang Huang, Jianming Yue, Xudong Zhu, Yeping Shi, Bingbing Shen, Qianmei Zhu, Lu Mei, Qiusheng Chen\",\"doi\":\"10.1096/fj.202501175RR\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Recent advancements have highlighted the imperative for cytological exploration of fascial tissues. Telocytes, specialized interstitial cells found in connective tissues such as fascia, have garnered significant attention. Our study explored the cellular landscape of the abdominal midline fascia (AMF), revealing a primary presence of Cd34+/Pdgfra+ telocytes (CPTCs) by single-cell sequencing and cytomorphology. We identified six CPTC subpopulations with deep learning, notably Ptgs2+ CPTCs, which exhibited remarkable responsiveness to mechanical stimulus. Following the acupuncture stimulation at the special acupoints along the AMF in dysenteric rats, the proportion of Ptgs2+ CPTCs increased significantly, with these cells exhibiting strengthened cell adhesion with all CPTC subpopulations. Importantly, Ptgs2+ CPTCs activated M2 macrophages through the Il6–Il6st–Stat3 pathway, promoting anti-inflammatory responses. For the first time, our findings established Ptgs2+ CPTCs as a key “force–immune axis” that linked mechanical stimulation and immune modulation, advancing our understanding of the cellular mechanisms behind acupuncture and its potential to modulate inflammation in immune-related disorders.</p>\",\"PeriodicalId\":50455,\"journal\":{\"name\":\"The FASEB Journal\",\"volume\":\"39 19\",\"pages\":\"\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-09-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12477662/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The FASEB Journal\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://faseb.onlinelibrary.wiley.com/doi/10.1096/fj.202501175RR\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The FASEB Journal","FirstCategoryId":"99","ListUrlMain":"https://faseb.onlinelibrary.wiley.com/doi/10.1096/fj.202501175RR","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Ptgs2+ CPTC Function as a “Force-Immune Axis” by Responding to Acupuncture and Mediating M2 Macrophage Activation for Anti-Inflammatory Effects
Recent advancements have highlighted the imperative for cytological exploration of fascial tissues. Telocytes, specialized interstitial cells found in connective tissues such as fascia, have garnered significant attention. Our study explored the cellular landscape of the abdominal midline fascia (AMF), revealing a primary presence of Cd34+/Pdgfra+ telocytes (CPTCs) by single-cell sequencing and cytomorphology. We identified six CPTC subpopulations with deep learning, notably Ptgs2+ CPTCs, which exhibited remarkable responsiveness to mechanical stimulus. Following the acupuncture stimulation at the special acupoints along the AMF in dysenteric rats, the proportion of Ptgs2+ CPTCs increased significantly, with these cells exhibiting strengthened cell adhesion with all CPTC subpopulations. Importantly, Ptgs2+ CPTCs activated M2 macrophages through the Il6–Il6st–Stat3 pathway, promoting anti-inflammatory responses. For the first time, our findings established Ptgs2+ CPTCs as a key “force–immune axis” that linked mechanical stimulation and immune modulation, advancing our understanding of the cellular mechanisms behind acupuncture and its potential to modulate inflammation in immune-related disorders.
期刊介绍:
The FASEB Journal publishes international, transdisciplinary research covering all fields of biology at every level of organization: atomic, molecular, cell, tissue, organ, organismic and population. While the journal strives to include research that cuts across the biological sciences, it also considers submissions that lie within one field, but may have implications for other fields as well. The journal seeks to publish basic and translational research, but also welcomes reports of pre-clinical and early clinical research. In addition to research, review, and hypothesis submissions, The FASEB Journal also seeks perspectives, commentaries, book reviews, and similar content related to the life sciences in its Up Front section.