TY - JOUR
T1 - Defining murine monocyte differentiation into colonic and ileal macrophages
AU - Gross-Vered, Mor
AU - Trzebanski, Sebastien
AU - Shemer, Anat
AU - Bernshtein, Biana
AU - Curato, Caterina
AU - Stelzer, Gil
AU - Salame, Tomer-Meir
AU - David, Eyal
AU - Boura-Halfon, Sigalit
AU - Chappell-Maor, Louise
AU - Leshkowitz, Dena
AU - Jung, Steffen
N1 - The authors declare no competing financial interests. We would like to thank all members of the Jung laboratory for helpful discussion. We further thank the staff of the Weizmann Animal facility and the members of the FACS facility for expert advice. Funding - European Research Council (340345), Steffen Jung The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication
PY - 2020/1/8
Y1 - 2020/1/8
N2 - Monocytes are circulating short-lived macrophage precursors that are recruited on demand from the blood to sites of inflammation and challenge. In steady state, classical monocytes give rise to vasculature-resident cells that patrol the luminal side of the endothelium. In addition, classical monocytes feed macrophage compartments of selected organs, including barrier tissues, such as the skin and intestine, as well as the heart. Monocyte differentiation under conditions of inflammation has been studied in considerable detail. In contrast, monocyte differentiation under non-inflammatory conditions remains less well understood. Here we took advantage of a combination of cell ablation and precursor engraftment to investigate the generation of gut macrophages from monocytes. Collectively, we identify factors associated with the gradual adaptation of monocytes to tissue residency. Moreover, comparison of monocyte differentiation into the colon and ileum-resident macrophages revealed the graduated acquisition of gut segment-specific gene expression signatures.
AB - Monocytes are circulating short-lived macrophage precursors that are recruited on demand from the blood to sites of inflammation and challenge. In steady state, classical monocytes give rise to vasculature-resident cells that patrol the luminal side of the endothelium. In addition, classical monocytes feed macrophage compartments of selected organs, including barrier tissues, such as the skin and intestine, as well as the heart. Monocyte differentiation under conditions of inflammation has been studied in considerable detail. In contrast, monocyte differentiation under non-inflammatory conditions remains less well understood. Here we took advantage of a combination of cell ablation and precursor engraftment to investigate the generation of gut macrophages from monocytes. Collectively, we identify factors associated with the gradual adaptation of monocytes to tissue residency. Moreover, comparison of monocyte differentiation into the colon and ileum-resident macrophages revealed the graduated acquisition of gut segment-specific gene expression signatures.
UR - http://www.scopus.com/inward/record.url?scp=85077724570&partnerID=8YFLogxK
U2 - 10.7554/eLife.49998
DO - 10.7554/eLife.49998
M3 - مقالة
SN - 2050-084X
VL - 9
JO - eLife
JF - eLife
M1 - e49998
ER -