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- W2548678995 abstract "Mononuclear phagocytes are a heterogeneous family that occupy all tissues and assume numerous roles to support tissue function and systemic homeostasis. Our ability to dissect the roles of individual subsets is limited by a lack of technologies that ablate gene function within specific mononuclear phagocyte sub-populations. Using Nr4a1-dependent Ly6Clow monocytes, we present a proof-of-principle approach that addresses these limitations. Combining ChIP-seq and molecular approaches we identified a single, conserved, sub-domain within the Nr4a1 enhancer that was essential for Ly6Clow monocyte development. Mice lacking this enhancer lacked Ly6Clow monocytes but retained Nr4a1 gene expression in macrophages during steady state and in response to LPS. Because Nr4a1 regulates inflammatory gene expression and differentiation of Ly6Clow monocytes, decoupling these processes allows Ly6Clow monocytes to be studied independently." @default.
- W2548678995 created "2016-11-11" @default.
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- W2548678995 date "2016-11-01" @default.
- W2548678995 modified "2023-10-14" @default.
- W2548678995 title "Deleting an Nr4a1 Super-Enhancer Subdomain Ablates Ly6C low Monocytes while Preserving Macrophage Gene Function" @default.
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- W2548678995 doi "https://doi.org/10.1016/j.immuni.2016.10.011" @default.
- W2548678995 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5694686" @default.
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