Macrophage and neutrophil heterogeneity at single-cell spatial resolution in human inflammatory bowel disease

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作者
Alba Garrido-Trigo
Ana M. Corraliza
Marisol Veny
Isabella Dotti
Elisa Melón-Ardanaz
Aina Rill
Helena L. Crowell
Ángel Corbí
Victoria Gudiño
Miriam Esteller
Iris Álvarez-Teubel
Daniel Aguilar
M. Carme Masamunt
Emily Killingbeck
Youngmi Kim
Michael Leon
Sudha Visvanathan
Domenica Marchese
Ginevra Caratù
Albert Martin-Cardona
Maria Esteve
Ingrid Ordás
Julian Panés
Elena Ricart
Elisabetta Mereu
Holger Heyn
Azucena Salas
机构
[1] Inflammatory Bowel Disease Unit,Department of Molecular Life Sciences
[2] Institut d’Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS),Centro de Investigaciones Biológicas
[3] Hospital Clínic,Translational Medicine and Clinical Pharmacology
[4] Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD),CNAG
[5] Josep Carreras Leukaemia Research Institute (IJC),CRG, Centre for Genomic Regulation (CRG)
[6] University of Zurich,Department of Gastroenterology
[7] Switzerland. SIB Swiss Institute of Bioinformatics,undefined
[8] Consejo Superior de Investigaciones Científicas (CSIC),undefined
[9] NanoString Technologies,undefined
[10] Boehringer-Ingelheim Pharmaceuticals Inc,undefined
[11] Barcelona Institute of Science and Technology (BIST),undefined
[12] Hospital Universitari Mútua Terrassa,undefined
[13] Universitat de Barcelona,undefined
[14] Universitat Pompeu Fabra (UPF),undefined
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摘要
Ulcerative colitis and Crohn’s disease are chronic inflammatory intestinal diseases with perplexing heterogeneity in disease manifestation and response to treatment. While the molecular basis for this heterogeneity remains uncharacterized, single-cell technologies allow us to explore the transcriptional states within tissues at an unprecedented resolution which could further understanding of these complex diseases. Here, we apply single-cell RNA-sequencing to human inflamed intestine and show that the largest differences among patients are present within the myeloid compartment including macrophages and neutrophils. Using spatial transcriptomics in human tissue at single-cell resolution (CosMx Spatial Molecular Imaging) we spatially localize each of the macrophage and neutrophil subsets identified by single-cell RNA-sequencing and unravel further macrophage diversity based on their tissue localization. Finally, single-cell RNA-sequencing combined with single-cell spatial analysis reveals a strong communication network involving macrophages and inflammatory fibroblasts. Our data sheds light on the cellular complexity of these diseases and points towards the myeloid and stromal compartments as important cellular subsets for understanding patient-to-patient heterogeneity.
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