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青少年特发性关节炎中的单细胞RNA测序

Single-cell RNA sequencing in juvenile idiopathic arthritis.

作者信息

Luo Xiwen, Tang Xuemei

机构信息

Department of Rheumatology and Immunology, Children's Hospital of Chongqing Medical University, Chongqing 400014, China.

Chongqing Key Laboratory of Child Infection and Immunity, Ministry of Education Key Laboratory of Child Development and Disorders, National Clinical Research Center for Child Health and Disorders, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, Children's Hospital of Chongqing Medical University, Chongqing 400014, China.

出版信息

Genes Dis. 2023 May 24;11(2):633-644. doi: 10.1016/j.gendis.2023.04.014. eCollection 2024 Mar.

DOI:10.1016/j.gendis.2023.04.014
PMID:37692495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10491939/
Abstract

Juvenile idiopathic arthritis (JIA) is one of the most common chronic inflammatory rheumatic diseases in children, with onset before age 16 and lasting for more than 6 weeks. JIA is a highly heterogeneous condition with various consequences for health and quality of life. For some JIA patients, early detection and intervention remain challenging. As a result, further investigation of the complex and unknown mechanisms underlying JIA is required. Advances in technology now allow us to describe the biological heterogeneity and function of individual cell populations in JIA. Through this review, we hope to provide novel ideas and potential targets for the diagnosis and treatment of JIA by summarizing the current findings of single-cell RNA sequencing studies and understanding how the major cell subsets drive JIA pathogenesis.

摘要

幼年特发性关节炎(JIA)是儿童中最常见的慢性炎症性风湿性疾病之一,发病于16岁之前,病程持续超过6周。JIA是一种高度异质性疾病,对健康和生活质量有各种影响。对于一些JIA患者来说,早期检测和干预仍然具有挑战性。因此,需要进一步研究JIA潜在的复杂未知机制。现在技术的进步使我们能够描述JIA中单个细胞群体的生物学异质性和功能。通过本综述,我们希望通过总结单细胞RNA测序研究的当前发现,并了解主要细胞亚群如何驱动JIA发病机制,为JIA的诊断和治疗提供新的思路和潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/10491939/7be26b9065ce/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/10491939/24afe82b84a0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/10491939/2f7e67145b56/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/10491939/7be26b9065ce/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/10491939/24afe82b84a0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/10491939/2f7e67145b56/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb1/10491939/7be26b9065ce/gr3.jpg

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本文引用的文献

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Cell Mol Biol Lett. 2023 Jan 23;28(1):6. doi: 10.1186/s11658-023-00418-z.
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Single-cell analysis reveals heterogeneity of juvenile idiopathic arthritis fibroblast-like synoviocytes with implications for disease subtype.单细胞分析揭示幼年特发性关节炎成纤维样滑膜细胞的异质性,提示疾病亚型的存在。
Arthritis Res Ther. 2022 Sep 27;24(1):225. doi: 10.1186/s13075-022-02913-8.
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GREM1 is required to maintain cellular heterogeneity in pancreatic cancer.
基于单细胞测序和孟德尔随机化分析揭示的慢性阻塞性肺疾病潜在标记基因。
Aging (Albany NY). 2024 May 23;16(10):8922-8943. doi: 10.18632/aging.205849.
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Comprehensive analysis of juvenile idiopathic arthritis patients' immune characteristics based on bulk and single-cell sequencing data.基于批量测序和单细胞测序数据对青少年特发性关节炎患者免疫特征的综合分析。
Front Mol Biosci. 2024 May 1;11:1359235. doi: 10.3389/fmolb.2024.1359235. eCollection 2024.
GREM1 对于维持胰腺癌中的细胞异质性是必需的。
Nature. 2022 Jul;607(7917):163-168. doi: 10.1038/s41586-022-04888-7. Epub 2022 Jun 29.
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Dissecting the Functional Role of the TRIM8 Protein on Cancer Pathogenesis.剖析TRIM8蛋白在癌症发病机制中的功能作用。
Cancers (Basel). 2022 May 6;14(9):2309. doi: 10.3390/cancers14092309.
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