Granulocyte Colony-Stimulating Factor Activating HIF-1a Acts Synergistically with Erythropoietin to PromoteTissue Plasticity
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Abstract
[[abstract]]"Stroke and peripheral limb ischemia are serious clinical problems with poor prognosis and limited treatment. The
cytokines erythropoietin (EPO) and granulocyte-colony stimulating factor (G-CSF) have been used to induce endogenous
cell repair and angiogenesis. Here, we demonstrated that the combination therapy of EPO and G-CSF exerted synergistic
effects on cell survival and functional recovery from cerebral and peripheral limbs ischemia. We observed that even under
normoxic conditions, G-CSF activates hypoxia-inducible factor-1a (HIF-1a), which then binds to the EPO promoter and
enhances EPO expression. Serum EPO level was significantly increased by G-CSF injection, with the exception of Tg-HIF-
1a
+f/+f
mice. The neuroplastic mechanisms exerted by EPO combined with G-CSF included enhanced expression of the
antiapoptotic protein of Bcl-2, augmented neurotrophic factors synthesis, and promoted neovascularization. Further, the
combination therapy significantly increased homing and differentiation of bone marrow stem cells (BMSCs) and intrinsic
neural progenitor cells (INPCs) into the ischemic area. In summary, EPO in combination with G-CSF synergistically
enhanced angiogenesis and tissue plasticity in ischemic animal models, leading to greater functional recovery than either
agent alone.