作者
Pranab K. Mukherjee,Quang Tam Nguyen,Jiannan Li,Shuai Zhao,Stephen M. Christensen,Gail West,Jyotsna Chandra,Ilyssa O. Gordon,Sinan Lin,Jie Wang,Ren Mao,D. Czarnecki,Carla Rayan,Prerna Kotak,Thomas Plesec,Samir Lal,Thomas Fabre,Shoh Asano,Kathryn Bound,Kevin M. Hart,Chanyoung Park,Robert Martinez,Ken Dower,Thomas A. Wynn,Shaomin Hu,Nayden G. Naydenov,Martin Decaris,Scott Turner,Stefan D. Holubar,Scott R. Steele,Claudio Fiocchi,Andrei I. Ivanov,Kellie M. Kravarik,Florian Rieder
摘要
Fibroblasts play a key role in stricture formation in Crohn's disease (CD) but understanding it's pathogenesis requires a systems-level investigation to uncover new treatment targets. We studied full thickness CD tissues to characterize fibroblast heterogeneity and function by generating the first single cell RNA sequencing (scRNAseq) atlas of strictured bowel and providing proof of principle for therapeutic target validation.