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Mafb lineage tracing to distinguish macrophages from other immune lineages reveals dual identity of Langerhans cells.


ABSTRACT: Current systems for conditional gene deletion within mouse macrophage lineages are limited by ectopic activity or low efficiency. In this study, we generated a Mafb-driven Cre strain to determine whether any dendritic cells (DCs) identified by Zbtb46-GFP expression originate from a Mafb-expressing population. Lineage tracing distinguished macrophages from classical DCs, neutrophils, and B cells in all organs examined. At steady state, Langerhans cells (LCs) were lineage traced but also expressed Zbtb46-GFP, a phenotype not observed in any other population. After exposure to house dust mite antigen, Zbtb46-negative CD64+ inflammatory cells infiltrating the lung were substantially lineage traced, but Zbtb46-positive CD64- cells were not. These results provide new evidence for the unique identity of LCs and challenge the notion that some inflammatory cells are a population of monocyte-derived DCs.

SUBMITTER: Wu X 

PROVIDER: S-EPMC5110021 | biostudies-literature | 2016 Nov

REPOSITORIES: biostudies-literature

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Mafb lineage tracing to distinguish macrophages from other immune lineages reveals dual identity of Langerhans cells.

Wu Xiaodi X   Briseño Carlos G CG   Durai Vivek V   Albring Jörn C JC   Haldar Malay M   Bagadia Prachi P   Kim Ki-Wook KW   Randolph Gwendalyn J GJ   Murphy Theresa L TL   Murphy Kenneth M KM  

The Journal of experimental medicine 20161017 12


Current systems for conditional gene deletion within mouse macrophage lineages are limited by ectopic activity or low efficiency. In this study, we generated a Mafb-driven Cre strain to determine whether any dendritic cells (DCs) identified by Zbtb46-GFP expression originate from a Mafb-expressing population. Lineage tracing distinguished macrophages from classical DCs, neutrophils, and B cells in all organs examined. At steady state, Langerhans cells (LCs) were lineage traced but also expressed  ...[more]

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