Comprehensive analysis of myeloid reporter mice

Yidan Wang(Northwestern University), Samuel D. Dowling(Northwestern University), Vanessa Rodríguez‐Fanjul(Northwestern University), Jessica Maciuch(Northwestern University), Meghan Mayer(Northwestern University), Tyler Therron(Northwestern University), Tovah N. Shaw(University of Edinburgh), Miranda G. Gurra(Northwestern University), Caroline L. Shah(Northwestern University), Hadijat-Kubura M. Makinde(Northwestern University), Florent Ginhoux(Singapore Immunology Network), David Voehringer(Friedrich-Alexander-Universität Erlangen-Nürnberg), Cole A. Harrington(The Ohio State University Wexner Medical Center), Toby Lawrence(King's College London), John R. Grainger(Manchester Academic Health Science Centre), Carla M. Cuda(Northwestern University), Deborah R. Winter(Northwestern University), Harris Perlman(Northwestern University)
bioRxiv (Cold Spring Harbor Laboratory)
February 27, 2025
Cited by 3Open Access
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Abstract

Macrophages are a pivotal cell type within the synovial lining and sub-lining of the joint, playing a crucial role in maintaining homeostasis of synovium. Although fate-mapping techniques have been employed to differentiate synovial macrophages from other synovial myeloid cells, no comprehensive study has yet been conducted within the mouse synovial macrophage compartment. In this study, we present, for the first time, lineage tracing results from 18 myeloid-specific fate-mapping models in mouse peripheral blood (PB) and synovial tissue. The identification of synovial macrophages and monocyte-lineage cells through flow cytometry was further validated using cellular indexing of transcriptomes and epitopes by sequencing (CITE-seq) datasets. These findings provide a valuable methodological tool for researchers to select appropriate models for studying the function of synovial myeloid cells and serve as a reference for investigations in other tissue types.


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