作者
Imke Liebold,Amirah Al Jawazneh,Christian Casar,Clarissa Lanzloth,Stephanie Leyk,Madeleine Hamley,Milagros N. Wong,Dominik Kylies,Stefanie K. Gräfe,Ilka Edenhofer,Irene Aranda-Pardos,Marie Kriwet,H. Haas,Jenny Krause,Alexandros Hadjilaou,Andra B. Schromm,Ulricke Richardt,Petra Eggert,Dennis Tappe,Sören Weidemann,Sourav Ghosh,Christian F. Krebs,Noelia A-González,Anna Worthmann,Ansgar W. Lohse,Samuel Huber,Carla V. Rothlin,Victor G. Puelles,Thomas Jacobs,Nicola Gagliani,Lidia Bosurgi
摘要
Macrophages are functionally heterogeneous cells essential for apoptotic cell clearance. Apoptotic cells are defined by homogeneous characteristics, ignoring their original cell lineage identity. We found that in an interleukin-4 (IL-4)-enriched environment, the sensing of apoptotic neutrophils by macrophages triggered their tissue remodeling signature. Engulfment of apoptotic hepatocytes promoted a tolerogenic phenotype, whereas phagocytosis of T cells had little effect on IL-4-induced gene expression. In a mouse model of parasite-induced pathology, the transfer of macrophages conditioned with IL-4 and apoptotic neutrophils promoted parasitic egg clearance. Knockout of phagocytic receptors required for the uptake of apoptotic neutrophils and partially T cells, but not hepatocytes, exacerbated helminth infection. These findings suggest that the identity of apoptotic cells may contribute to the development of distinct IL-4-driven immune programs in macrophages.