Toll-Like Receptor 7-Expressed Macrophages Are Involved in the Pathogenesis of Esophageal Achalasia and Esophagogastric Junction Outflow Obstruction.

IF 3 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Digestion Pub Date : 2024-08-05 DOI:10.1159/000540693
Masatoshi Kaizuka, Tetsuya Tatsuta, Shogo Kawaguchi, Tadashi Yoshizawa, Shukuko Yoshida, Tetsuyuki Tateda, Yohei Sawada, Shinji Ota, Shiro Hayamizu, Keisuke Hasui, Hidezumi Kikuchi, Hiroto Hiraga, Daisuke Chinda, Takahiro Muroya, Kenichi Hakamada, Hiroshi Kijima, Tatsuya Mikami, Shinsaku Fukuda, Hirotake Sakuraba
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引用次数: 0

Abstract

Introduction: Esophageal achalasia is a typical esophageal motility disorder (EMD). Although viral infections have been hypothesized to play a role in the pathogenesis of esophageal achalasia, its etiology remains unclear. This study used esophageal muscle layer specimens collected during per-oral endoscopic myotomy (POEM) procedures to investigate the association between esophageal achalasia and esophagogastric junction outflow obstruction (EGJOO) and pattern recognition receptors.

Methods: Patients with esophageal achalasia and EGJOO who underwent POEM were allocated to the EMD group. Biopsies of the inner circular muscle were conducted during the POEM procedure. The control group comprised individuals diagnosed with esophageal squamous cell carcinoma who underwent surgical resection. Expression of pattern recognition receptors, including Toll-like receptor (TLR) 7, was examined by polymerase chain reaction. Immunohistochemical staining was performed to determine TLR7 expression sites in the esophageal muscle layer, and the relationship between TLR7 mRNA expression and clinical score was investigated.

Results: Our analysis revealed a notable upregulation of TLR7 mRNA levels within the muscle layer of esophageal achalasia and EGJOO, in contrast to those of control specimens. In contrast, the correlation between TLR7 and clinical score was not significant. Immunohistochemical staining revealed increased numbers of TLR7-expressing macrophages between the muscle layers.

Conclusions: TLR7-expressing macrophages are involved in the innate immune response underlying esophageal achalasia and EGJOO. This result will lead to the elucidation of new pathogenetic mechanisms and the development of novel therapeutic targets.

表达 Toll 样受体 7 的巨噬细胞参与了食管贲门失弛缓症、贲门失弛缓症和食管胃交界处流出道梗阻的发病机制。
简介食管贲门失弛缓症是一种典型的食管运动障碍(EMD)。虽然病毒感染被假定在食道贲门失弛缓症的发病机制中发挥作用,但其病因仍不清楚。本研究利用在经口内窥镜肌切开术(POEM)过程中采集的食管肌层标本,研究食管贲门失弛缓症与食管胃交界流出道梗阻(EGJOO)和模式识别受体之间的关联:方法:接受 POEM 手术的食管贲门失弛缓症和 EGJOO 患者被分配到 EMD 组。在 POEM 过程中对内环肌进行活检。对照组包括接受手术切除的食管鳞状细胞癌患者。聚合酶链反应检测了模式识别受体(包括 Toll 样受体 (TLR) 7)的表达。通过免疫组化染色确定食管肌层的 TLR7 表达位点,并研究 TLR7 mRNA 表达与临床评分之间的关系:结果:我们的分析发现,与对照标本相比,食管贲门失弛缓症和 EGJOO 的肌层中 TLR7 mRNA 水平明显上调。相比之下,TLR7 与临床评分之间的相关性并不显著。免疫组化染色显示,肌层之间表达 TLR7 的巨噬细胞数量增加:结论:表达 TLR7 的巨噬细胞参与了食管贲门失弛缓症和 EGJOO 的先天性免疫反应。结论:TLR7 表达的巨噬细胞参与了食管贲门失弛缓症和 EGJOO 的先天性免疫反应,这一结果将有助于阐明新的发病机制和开发新的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Digestion
Digestion 医学-胃肠肝病学
CiteScore
7.90
自引率
0.00%
发文量
39
审稿时长
6-12 weeks
期刊介绍: ''Digestion'' concentrates on clinical research reports: in addition to editorials and reviews, the journal features sections on Stomach/Esophagus, Bowel, Neuro-Gastroenterology, Liver/Bile, Pancreas, Metabolism/Nutrition and Gastrointestinal Oncology. Papers cover physiology in humans, metabolic studies and clinical work on the etiology, diagnosis, and therapy of human diseases. It is thus especially cut out for gastroenterologists employed in hospitals and outpatient units. Moreover, the journal''s coverage of studies on the metabolism and effects of therapeutic drugs carries considerable value for clinicians and investigators beyond the immediate field of gastroenterology.
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