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单细胞测序数据鉴定出狭窄型克罗恩病中独特的 B 细胞和成纤维细胞群体。

Single cell sequencing data identify distinct B cell and fibroblast populations in stricturing Crohn's disease.

机构信息

Victor Chang Cardiac Research Institute, Sydney, New South Wales, Australia.

St Vincent's Clinical School, University of New South Wales, Sydney, New South Wales, Australia.

出版信息

J Cell Mol Med. 2024 May;28(9):e18344. doi: 10.1111/jcmm.18344.

Abstract

Single cell RNA sequencing of human full thickness Crohn's disease (CD) small bowel resection specimens was used to identify potential therapeutic targets for stricturing (S) CD. Using an unbiased approach, 16 cell lineages were assigned within 14,539 sequenced cells from patient-matched SCD and non-stricturing (NSCD) preparations. SCD and NSCD contained identical cell types. Amongst immune cells, B cells and plasma cells were selectively increased in SCD samples. B cell subsets suggested formation of tertiary lymphoid tissue in SCD and compared with NSCD there was an increase in IgG, and a decrease in IgA plasma cells, consistent with their potential role in CD fibrosis. Two Lumican-positive fibroblast subtypes were identified and subclassified based on expression of selectively enriched genes as fibroblast clusters (C) 12 and C9. Cells within these clusters expressed the profibrotic genes Decorin (C12) and JUN (C9). C9 cells expressed ACTA2; ECM genes COL4A1, COL4A2, COL15A1, COL6A3, COL18A1 and ADAMDEC1; LAMB1 and GREM1. GO and KEGG Biological terms showed extracellular matrix and stricture organization associated with C12 and C9, and regulation of WNT pathway genes with C9. Trajectory and differential gene analysis of C12 and C9 identified four sub-clusters. Intra sub-cluster gene analysis detected 13 co-regulated gene modules that aligned along predicted pseudotime trajectories. CXCL14 and ADAMDEC1 were key markers in module 1. Our findings support further investigation of fibroblast heterogeneity and interactions with local and circulating immune cells at earlier time points in fibrosis progression. Breaking these interactions by targeting one or other population may improve therapeutic management for SCD.

摘要

采用单细胞 RNA 测序技术对人类全层克罗恩病(CD)小肠切除术标本进行分析,以确定狭窄(S)CD 的潜在治疗靶点。使用无偏方法,在来自患者匹配的 SCD 和非狭窄(NSCD)制剂的 14539 个测序细胞中分配了 16 种细胞谱系。SCD 和 NSCD 包含相同的细胞类型。在免疫细胞中,B 细胞和浆细胞在 SCD 样本中选择性增加。B 细胞亚群表明 SCD 中形成了三级淋巴组织,与 NSCD 相比,IgG 增加,IgA 浆细胞减少,这与其在 CD 纤维化中的潜在作用一致。鉴定出两种阳性亮氨酸纤维蛋白原的成纤维细胞亚型,并根据选择性富集基因的表达将其分为纤维母细胞簇(C)12 和 C9。这些簇中的细胞表达了促纤维化基因 Decorin(C12)和 JUN(C9)。C9 细胞表达 ACTA2;细胞外基质基因 COL4A1、COL4A2、COL15A1、COL6A3、COL18A1 和 ADAMDEC1;LAMB1 和 GREM1。GO 和 KEGG 生物学术语显示与 C12 和 C9 相关的细胞外基质和狭窄组织以及 C9 中的 WNT 途径基因调节。C12 和 C9 的轨迹和差异基因分析确定了四个亚群。亚群内基因分析检测到 13 个共同调节的基因模块,这些模块沿着预测的伪时间轨迹排列。CXCL14 和 ADAMDEC1 是模块 1 中的关键标记物。我们的研究结果支持进一步研究纤维化进展早期成纤维细胞异质性及其与局部和循环免疫细胞的相互作用。通过靶向一个或另一个群体来打破这些相互作用可能会改善 SCD 的治疗管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/134c/11058334/24f4ad30c9ab/JCMM-28-e18344-g001.jpg

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