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内源性大麻素系统在嗜酸性食管炎期间驱动嗜酸性粒细胞浸润。

The Endocannabinoid System Drives Eosinophil Infiltration During Eosinophilic Esophagitis.

作者信息

Gruden Eva, Kienzl Melanie, Danner Laura, Kaspret David Markus, Pammer Anja, Ristic Dusica, Kindler Oliver, Doyle Alfred D, Wright Benjamin L, Taschler Ulrike, Thomas Dominique, Gurke Robert, Baumann-Durchschein Franziska, Konrad Julia, Blesl Andreas, Schlager Hansjörg, Bärnthaler Thomas, Kargl Julia, Schicho Rudolf

机构信息

Division of Pharmacology, Otto Loewi Research Center, Medical University of Graz, Graz, Austria.

Division of Pharmacology, Otto Loewi Research Center, Medical University of Graz, Graz, Austria.

出版信息

Cell Mol Gastroenterol Hepatol. 2025 Apr 11;19(8):101515. doi: 10.1016/j.jcmgh.2025.101515.

Abstract

BACKGROUND AND AIMS

Eosinophilic esophagitis (EoE) is a chronic, inflammatory, and antigen-driven disease of the esophagus. Total transcriptome data revealed alterations in the endocannabinoid system, in particular, down-regulation of monoacylglycerol lipase (MGL) in biopsies of patients with active EoE. We investigated the consequence of MGL down-regulation in mucosal biopsies of patients, and its implications for EoE development, such as recruitment of eosinophils.

METHODS

Levels of MGL substrate 2-arachidonoylglycerol, MGL enzyme activity, and MGL colocalization with epithelial cells were determined in mucosal esophageal biopsies of patients with EoE. Supernatant of human primary esophageal epithelial cells was used to determine eosinophil migration and activation. An inducible mouse model of EoE was used to test MGL inhibition and cannabinoid (CB) receptor antagonism in vivo.

RESULTS

MGL expression in esophageal epithelial cells from patients with active EoE is decreased, whereas 2-arachidonoylglycerol is increased compared with control subjects. Inhibition of MGL in epithelial cells leads to a proinflammatory phenotype capable of attracting eosinophils via CB. Similarly, the EoE mouse model indicates that absence of MGL results in higher eosinophil infiltration. Targeting CB reduced the number of infiltrating eosinophils in the esophagi of mice.

CONCLUSIONS

This study is the first of its kind to investigate the involvement of altered expression of endocannabinoid system components in EoE, and partly explains recent findings of more inflammatory features post EoE-treatment in cannabis users. Our findings could pave the way for research into alternative treatment options for EoE and call for caution regarding the use of cannabinoids in EoE.

摘要

背景与目的

嗜酸性食管炎(EoE)是一种食管的慢性、炎症性且由抗原驱动的疾病。全转录组数据显示内源性大麻素系统存在改变,尤其是在活动性EoE患者的活检组织中,单酰甘油脂肪酶(MGL)表达下调。我们研究了MGL下调在患者黏膜活检组织中的后果,及其对EoE发展的影响,如嗜酸性粒细胞的募集。

方法

在EoE患者的食管黏膜活检组织中测定MGL底物2-花生四烯酸甘油酯的水平、MGL酶活性以及MGL与上皮细胞的共定位情况。用人原代食管上皮细胞的上清液来测定嗜酸性粒细胞的迁移和活化。使用EoE诱导小鼠模型在体内测试MGL抑制和大麻素(CB)受体拮抗作用。

结果

与对照组相比,活动性EoE患者食管上皮细胞中的MGL表达降低,而2-花生四烯酸甘油酯增加。上皮细胞中MGL的抑制导致一种促炎表型,能够通过CB吸引嗜酸性粒细胞。同样,EoE小鼠模型表明MGL缺失会导致更高的嗜酸性粒细胞浸润。靶向CB可减少小鼠食管中浸润的嗜酸性粒细胞数量。

结论

本研究首次调查了内源性大麻素系统成分表达改变在EoE中的作用,部分解释了近期在大麻使用者中EoE治疗后出现更多炎症特征的发现。我们的研究结果可能为EoE替代治疗方案的研究铺平道路,并呼吁在EoE中使用大麻素时要谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5729/12143766/c76e2d463ff4/ga1.jpg

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