Recent studies have shown that tissue macrophages (MΦ) arise from embryonic progenitors of the yolk sac (YS) and fetal liver and colonize tissues before birth. Further studies have proposed that developmentally distinct tissue MΦ can be identified based on the differential expression of F4/80 and CD11b, but whether a characteristic transcriptional profile exists is largely unknown. Here, we took advantage of an inducible fate‐mapping system that facilitated the identification of CD45+c‐kit−CX3CR1+F4/80+ (A2) progenitors of the YS as the source of F4/80hi but not CD11bhi MΦ. Large‐scale transcriptional profiling of MΦ precursors from the YS stage to adulthood allowed for building computational models for F4/80hi tissue macrophages being direct descendants of A2 progenitors. We further identified a distinct molecular signature of F4/80hi and CD11bhi MΦ and found that Irf8 was vital for MΦ maturation. Our data provide new cellular and molecular insights into the origin and developmental pathways of tissue MΦ.
Unit 1
Unit 1: Genetik, Entwicklungsbiologie & Molekulare Physiologie
- Michael Hoch/Reinhard Bauer: Entwicklungsgenetik & Molekulare Physiologie
- Elvira Mass: Entwicklungsbiologie des Immunsystems
- Michael Pankratz: Molekulare Hirnphysiologie & Verhaltensforschung
- Dietmar Schmucker: Entwicklung neuronaler Verschaltungen
Unit 2
Unit 2: Molekulare Immun- & Zellbiologie
- Sven Burgdorf: Zelluläre Immunologie
- Irmgard Förster: Immunologie & Umwelt
- Jan Hasenauer: Rechnergestützte Lebenswissenschaften
- Eva Kiermaier: Immun- und Tumorbiologie
- Waldemar Kolanus: Molekulare Immunologie und Zellbiologie
- Mihai Netea: Immunologie und Metabolismus
- Joachim Schultze: Genomik & Immunregulation
- Ivonne Vazquez Armendariz: Organoide Biologie
- Andreas Schlitzer: Biologie der Entzündung
Unit 3
Unit 4
Ehemalige Gruppen
Sie sind hier:



