滑膜
病理
关节炎
细胞
化学
医学
免疫学
生物化学
作者
Sam G. Edalat,Reto Gerber,Miranda Houtman,Janine Lückgen,R. L. Teixeira,Maria Del Pilar Palacios Cisneros,Tamara Pfanner,Tadeja Kuret,Nadja Ižanc,Raphael Micheroli,Joaquim Polido‐Pereira,Fernando Saraiva,Swathi Lingam,Kristina Bürki,Blaž Burja,Chantal Pauli,Žiga Rotar,Matija Tomšič,Saša Čučnik,João Eurico Fonseca
出处
期刊:iScience
[Cell Press]
日期:2024-04-10
卷期号:27 (6): 109707-109707
被引量:4
标识
DOI:10.1016/j.isci.2024.109707
摘要
In this study, we optimized the dissociation of synovial tissue biopsies for single-cell omics studies and created a single-cell atlas of human synovium in inflammatory arthritis. The optimized protocol allowed consistent isolation of highly viable cells from tiny fresh synovial biopsies, minimizing the synovial biopsy drop-out rate. The synovium scRNA-seq atlas contained over 100,000 unsorted synovial cells from 25 synovial tissues affected by inflammatory arthritis, including 16 structural, 11 lymphoid, and 15 myeloid cell clusters. This synovial cell map expanded the diversity of synovial cell types/states, detected synovial neutrophils, and broadened synovial endothelial cell classification. We revealed tissue-resident macrophage subsets with proposed matrix-sensing (FOLR2+COLEC12
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