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      Stroma-derived interleukin-34 controls the development and maintenance of langerhans cells and the maintenance of microglia.

      Immunity
      Animals, Brain, immunology, metabolism, Cell Differentiation, genetics, Epidermis, Homeostasis, Humans, Inflammation, Interleukins, physiology, Keratinocytes, Langerhans Cells, cytology, Mice, Microglia, Psoriasis, chemically induced, Receptor, Macrophage Colony-Stimulating Factor, Signal Transduction, Skin, Stromal Cells

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          Abstract

          Colony stimulating factor-1 (Csf-1) receptor and its ligand Csf-1 control macrophage development, maintenance, and function. The development of both Langerhans cells (LCs) and microglia is highly dependent on Csf-1 receptor signaling but independent of Csf-1. Here we show that in both mice and humans, interleukin-34 (IL-34), an alternative ligand for Csf-1 receptor, is produced by keratinocytes in the epidermis and by neurons in the brain. Mice lacking IL-34 displayed a marked reduction of LCs and a decrease of microglia, whereas monocytes, dermal, and lymphoid tissue macrophages and DCs were unaffected. We identified IL-34 as a nonredundant cytokine for the development of LCs during embryogenesis as well as for their homeostasis in the adult skin. Whereas inflammation-induced repopulation of LCs appears to be dependent on Csf-1, once inflammation is resolved, LC survival is again IL-34-dependent. In contrast, microglia and their yolk sac precursors develop independently of IL-34 but rely on it for their maintenance in the adult brain. Copyright © 2012 Elsevier Inc. All rights reserved.

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