Origins and functional specialization of macrophages and of conventional and monocyte-derived dendritic cells in mouse skin.
By Samira Tamoutounour, M. Guilliams, Frédéric Montañana Sanchis, Hong Liu, D. Terhorst, C. Malosse, É. Pollet, L. Ardouin, H. Luche, Cindy Sanchez and 3 more. Immunity, 2013
734 citations recorded by the source corpus.
Subfields: Immunology
View Paper: https://www.semanticscholar.org/paper/635234bed33c89ab8095a4fc56cfec78ea9dbe11
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In Immunology
Citations in the corpus
- Unsupervised High-Dimensional Analysis Aligns Dendritic Cells across Tissues and Species (2016, background): “…on next page) 670 Immunity 45, 669–684, September 20, 2016 many murine Macs can express the prototypical cDC markers CD11c or MHCII and, conversely, that cDC2 can express the Mac marker F4/80 (Bain et al., 2012; Schlitzer et al., 2015; Scott et al., 2015; Tamoutounour et al., 2012, 2013).”
- Developmental and Functional Heterogeneity of Monocytes. (2018, background): “, 2012), dermis (Tamoutounour et al., 2013), heart (Epelman et al.”
- From Monocytes to M1/M2 Macrophages: Phenotypical vs. Functional Differentiation (2014, background): “Conversely, in the dermis are present both resident dermal macrophages and monocyte-derived macrophages (60, 61).”
- Origin and Functions of Tissue Macrophages (2014, result): “However, 25% of skin macrophages were not replaced, even after 1 year posttransplant, suggesting that some human skin resident macrophages might persist independently of circulating monocyte input, which is similar to what has been observed in mice (Jakubzick et al., 2013; Tamoutounour et al., 2013)”
- Two distinct interstitial macrophage populations coexist across tissues in specific subtissular niches (2019, background): “Subpopulations of MHCII versus MHCII dermal macrophages (47), as well as dermal perivascular macrophages (48, 49), have already been described.”
- Tissue-Resident Macrophage Ontogeny and Homeostasis. (2016, background): “…that macrophage populations in these sites are significantly reduced in mice lacking this chemokine receptor (Bain et al., 2014; Platt et al., 2010; Zigmond et al., 2012) and originate almost exclusively from wild-type BM-derived cells in WT:Ccr2 / competitive chimeras (Tamoutounour et al., 2013).”