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粪便粘蛋白MUC2在多发性硬化症中减少,且与粘蛋白降解细菌有关。

Faecal mucoprotein MUC2 is decreased in multiple sclerosis and is associated with mucin degrading bacteria.

作者信息

Schwerdtfeger Luke A, Montini Federico, Chitnis Tanuja, Cox Laura M, Weiner Howard L

机构信息

Ann Romney Center for Neurologic Diseases, Harvard Medical School, Brigham and Women's Hospital, Boston, MA, USA.

Ann Romney Center for Neurologic Diseases, Harvard Medical School, Brigham and Women's Hospital, Boston, MA, USA.

出版信息

EBioMedicine. 2025 Jun;116:105721. doi: 10.1016/j.ebiom.2025.105721. Epub 2025 May 8.

Abstract

BACKGROUND

The gut microbiome is altered in MS and may contribute to disease by disrupting the intestinal barrier. The colonic mucus barrier, which is primarily composed of mucin protein 2 (MUC2), plays a crucial role in providing a barrier between colonic epithelial cells and the microbiome. Disruption of intestinal epithelial and mucus barriers has been reported in inflammatory bowel disease (IBD) and Parkinson's disease (PD) but has not been studied in the context of the microbiome in multiple sclerosis (MS).

METHODS

We investigated the epithelial tight junction protein zonulin occludins 1 (ZO-1), mucus protein MUC2, inflammatory stool markers (calprotectin), and gut microbiota composition in a cohort of subjects with relapsing and progressive MS.

FINDINGS

MUC2 was decreased in stool of subjects with both relapsing and progressive MS. ZO-1 was elevated in the serum of subjects with progressive MS but was not altered in the stool. Inflammatory markers typically elevated in IBD and PD, including calprotectin, were not altered in MS stool, suggesting disease specificity of altered gut physiology in MS. Microbiota with known mucus degrading capacity were elevated in the stool of subjects with MS and negatively correlated with mucus protein levels.

INTERPRETATION

Taken together, these findings suggest reduced gut barrier function in MS which is linked to increased mucin degrading bacteria.

FUNDING

This work was supported by grants from the National MS Society, the NIH/NINDS, the Nancy Davis Race to Erase MS Young Investigator Award, the Water Cove Charitable Foundation, and the Clara E. and John H. Ware Jr.

摘要

背景

肠道微生物群在多发性硬化症(MS)中发生改变,可能通过破坏肠道屏障导致疾病。结肠黏液屏障主要由黏蛋白2(MUC2)组成,在结肠上皮细胞与微生物群之间提供屏障方面发挥着关键作用。炎症性肠病(IBD)和帕金森病(PD)中已报道肠道上皮和黏液屏障受到破坏,但尚未在多发性硬化症(MS)微生物群背景下进行研究。

方法

我们调查了复发型和进展型MS患者队列中的上皮紧密连接蛋白闭合蛋白1(ZO-1)、黏液蛋白MUC2、炎症性粪便标志物(钙卫蛋白)和肠道微生物群组成。

研究结果

复发型和进展型MS患者粪便中的MUC2均减少。进展型MS患者血清中的ZO-1升高,但粪便中未改变。IBD和PD中通常升高的炎症标志物,包括钙卫蛋白,在MS粪便中未改变,表明MS中肠道生理改变具有疾病特异性。具有已知黏液降解能力的微生物群在MS患者粪便中升高,且与黏液蛋白水平呈负相关。

解读

综上所述,这些发现表明MS患者肠道屏障功能降低,这与黏蛋白降解细菌增加有关。

资助

这项工作得到了美国国家多发性硬化症协会、美国国立卫生研究院/国立神经疾病与中风研究所、南希·戴维斯消除多发性硬化症竞赛青年研究员奖、水湾慈善基金会以及克拉拉·E.和小约翰·H.韦尔的资助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/12134549/131fdeb1d44c/gr1.jpg

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