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溃疡性结肠炎:单细胞RNA测序提供的上皮新见解

Ulcerative Colitis: Novel Epithelial Insights Provided by Single Cell RNA Sequencing.

作者信息

Serigado Joao M, Foulke-Abel Jennifer, Hines William C, Hanson Joshua A, In Julie, Kovbasnjuk Olga

机构信息

Division of Gastroenterology and Hepatology, Department of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM, United States.

Division of Gastroenterology and Hepatology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States.

出版信息

Front Med (Lausanne). 2022 Apr 20;9:868508. doi: 10.3389/fmed.2022.868508. eCollection 2022.

DOI:10.3389/fmed.2022.868508
PMID:35530046
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9068527/
Abstract

Ulcerative Colitis (UC) is a chronic inflammatory disease of the intestinal tract for which a definitive etiology is yet unknown. Both genetic and environmental factors have been implicated in the development of UC. Recently, single cell RNA sequencing (scRNA-seq) technology revealed cell subpopulations contributing to the pathogenesis of UC and brought new insight into the pathways that connect genome to pathology. This review describes key scRNA-seq findings in two major studies by Broad Institute and University of Oxford, investigating the transcriptomic landscape of epithelial cells in UC. We focus on five major findings: (1) the identification of BEST4 + cells, (2) colonic microfold (M) cells, (3) detailed comparison of the transcriptomes of goblet cells, and (4) colonocytes and (5) stem cells in health and disease. In analyzing the two studies, we identify the commonalities and differences in methodologies, results, and conclusions, offering possible explanations, and validated several cell cluster markers. In systematizing the results, we hope to offer a framework that the broad scientific GI community and GI clinicians can use to replicate or corroborate the extensive new findings that RNA-seq offers.

摘要

溃疡性结肠炎(UC)是一种肠道慢性炎症性疾病,其确切病因尚不清楚。遗传和环境因素都与UC的发病有关。最近,单细胞RNA测序(scRNA-seq)技术揭示了参与UC发病机制的细胞亚群,并为连接基因组与病理学的途径带来了新的见解。这篇综述描述了布罗德研究所和牛津大学两项主要研究中的关键scRNA-seq研究结果,这些研究调查了UC上皮细胞的转录组图谱。我们重点关注五个主要发现:(1)BEST4+细胞的鉴定,(2)结肠微褶(M)细胞,(3)杯状细胞转录组的详细比较,(4)结肠细胞,以及(5)健康和疾病状态下的干细胞。在分析这两项研究时,我们确定了方法、结果和结论中的异同,给出了可能的解释,并验证了几种细胞簇标记。在对结果进行系统化整理时,我们希望提供一个框架,广大胃肠科学领域的科研人员和胃肠科临床医生可以利用该框架来重复或证实RNA测序提供的大量新发现。

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Excessive Apoptosis in Ulcerative Colitis: Crosstalk Between Apoptosis, ROS, ER Stress, and Intestinal Homeostasis.溃疡性结肠炎中的细胞凋亡过度:细胞凋亡、ROS、内质网应激与肠道内稳态的串扰。
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Integrated single-cell and bulk RNA sequencing reveals CREM is involved in the pathogenesis of ulcerative colitis.整合单细胞和批量RNA测序揭示CREM参与溃疡性结肠炎的发病机制。
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Cronkhite‒Canada syndrome as inflammatory hamartomatous polyposis: new evidence from whole transcriptome sequencing of colonic polyps.克罗恩病-加拿大综合征作为炎症性错构瘤性息肉病:来自结肠息肉全转录组测序的新证据。
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M1 and M2 Macrophages Differentially Regulate Colonic Crypt Renewal.M1 和 M2 巨噬细胞对结肠隐窝更新的调控存在差异。
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Identification of Novel Population-Specific Cell Subsets in Chinese Ulcerative Colitis Patients Using Single-Cell RNA Sequencing.利用单细胞 RNA 测序鉴定中国溃疡性结肠炎患者中的新型群体特异性细胞亚群。
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