Neuroprotective signaling pathways employed by Erythropoietin

Neuroprotective signaling pathways employed by Erythropoietin. During a hypoxic event, HIF-1a stabilization is promoted, which in turn activates hypoxia-sensitive genes (including EPO) inducing transcription of endogenous EPO. Endogenous and exogenous EPO are capable of binding the extracellular EPO receptor (EPOR), causing its homodimerization. Once EPO has coupled with EPOR, JAK2 is phosphorylated leading to several downstream signaling pathways including Ras-mitogen activated protein kinase (MAPK), phosphatidylinositol-3-kinase/protein kinase B (PI3K/AKT) and the transcription factor signal transducers and activators of transcription-5 (STAT-5). PI3-K activation leads to AKT phosphorylation which may inhibit GSK3 and subsequent caspase formation. Moreover, AKT inhibits p53 activity through mdm2 activation (p53 acts as pro-apoptotic by stimulating cytochrome c release from mitochondria via Bad/Bax) leading to a diminished cytochrome c release through inhibition of Bad/Bax functioning. Additionally, EPO has been shown to enhance the antioxidant defense mechanisms, which are possible after unbounding of NFk-B from its inactive complex, which in turn induces transcription of p53, x-lynked (xIAP) and cellular (cIAP) inhibitors of apoptosis, superoxide dismutase and anti-apoptotic genes (Bcl-2 and Bcl-xL). Nuclear transcription of Bcl-2 and Bcl-xL is also possible via the STAT-5 pathway induced by JAK2 phosphorylation. Binding of EPO to its receptor (EPOR) on the endothelial cells leads to phosphorylation of JAK2, which activates PI3-K/AKT pathway, causing endothelial nitric oxide (NO) synthase phosphorylation; then increasing NO production resulting in cerebral vasodilation. Finally, EPO also induces Ras-Raf pathway, activating MAPK leading to phosphorylation of ERK-1/2 inducing the transcription of anti-apoptotic genes.

Publication

Erythropoietin Neuroprotection with Traumatic Brain Injury. () Lucido L. Ponce, et al. Pathophysiology. ;20(1):31-38. Figure: F1. All organisms Drosophila melanogaster Homo sapiens

Disease mentions