Figure 3
Figure 3. Role of KLFs in myeloid development, renewal, and activation. (A) KLF4 and PU.1 are expressed in a stage-specific pattern during myelopoiesis (adapted with permission; see Feinberg et al62). (B-F) Overexpression of KLF4 in CMPs or HSCs promotes exclusive monocyte differentiation, whereas PU.1 promotes both monocytic and granulocytic differentiation (adapted with permission; see Feinberg et al62). (G) Schematic overview of KLFs in monocyte biology. KLF4 is a downstream target gene of PU.1 that promotes monocyte differentiation from hematopoietic stem cell progenitors. High expression levels of KLF4 and c-Myc enable differentiated monocytes/macrophages capable of self-renewal, an effect regulated by MafB and c-Maf and potentially mediated by their respective downstream targets, PU.1 and Ets1/2. Statins induce KLF2, which can repress genes involved in macrophage activation. KLF4 promotes the development of inflammatory monocytes (Ly-6C+, CD62L+, CCR2+) in blood and tissues and, to a lesser extent, resident macrophages in tissues (Ly6C−, CD62L−, CCR2−).

Role of KLFs in myeloid development, renewal, and activation. (A) KLF4 and PU.1 are expressed in a stage-specific pattern during myelopoiesis (adapted with permission; see Feinberg et al62 ). (B-F) Overexpression of KLF4 in CMPs or HSCs promotes exclusive monocyte differentiation, whereas PU.1 promotes both monocytic and granulocytic differentiation (adapted with permission; see Feinberg et al62 ). (G) Schematic overview of KLFs in monocyte biology. KLF4 is a downstream target gene of PU.1 that promotes monocyte differentiation from hematopoietic stem cell progenitors. High expression levels of KLF4 and c-Myc enable differentiated monocytes/macrophages capable of self-renewal, an effect regulated by MafB and c-Maf and potentially mediated by their respective downstream targets, PU.1 and Ets1/2. Statins induce KLF2, which can repress genes involved in macrophage activation. KLF4 promotes the development of inflammatory monocytes (Ly-6C+, CD62L+, CCR2+) in blood and tissues and, to a lesser extent, resident macrophages in tissues (Ly6C, CD62L, CCR2).

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