Tumor Necrosis Factor α Primes Cerebral Endothelial Cells for Erythropoietin-Induced Angiogenesis
Author(s) -
Lei Wang,
Michael Chopp,
Hua Teng,
Marianne Bolz,
Francisco Moniche,
Danielle Marie Aluigi,
Xin Li Wang,
Rui Lan Zhang,
Søren Chrsitensen,
Thomas N. Sager,
Alexandra Szalad,
Zheng Gang Zhang
Publication year - 2010
Publication title -
journal of cerebral blood flow and metabolism
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.167
H-Index - 193
eISSN - 1559-7016
pISSN - 0271-678X
DOI - 10.1038/jcbfm.2010.138
Subject(s) - erythropoietin receptor , angiogenesis , erythropoietin , vascular endothelial growth factor , downregulation and upregulation , endothelial stem cell , tumor necrosis factor alpha , endocrinology , vascular endothelial growth factor a , vascular endothelial growth factor b , cancer research , medicine , biology , microbiology and biotechnology , in vitro , biochemistry , vegf receptors , gene
Erythropoietin (EPO) enhances angiogenesis in the ischemic brain. Stroke induces secretion of tumor necrosis factor α (TNF-α). We investigated the effect of TNF-α on EPO-induced in vitro angiogenesis in cerebral endothelial cells. Using a capillary-like tubular formation assay, we found that transient incubation of primary rat cerebral microvascular endothelial cells (RECs) with TNF-α substantially upregulated EPO receptor (EPOR) expression and addition of EPO into TNF-α-treated RECs significantly augmented the capillary-like tube formation. Blockage of TNF receptor 1 (TNFR1) suppressed TNF-α-upregulated EPOR expression and abolished EPO-induced tube formation. Attenuation of endogenous EPOR with small interfering RNA (siRNA) also inhibited EPO-enhanced tube formation. Treatment of RECs with EPO activated nuclear factor-kappa B (NF-κB) and Akt. Incubation of the TNF-α-treated endothelial cells with EPO activated vascular endothelial growth factor (VEGF), VEGF receptor 2 (VEGFR2), angiopoietin 1 (Ang1), and Tie2. Blockage of VEGFR2 and Tie2 resulted in reduction of EPO-augmented tube formation. These data indicate that interaction of TNF-α with TNFR1 sensitizes cerebral endothelial cells for EPO-induced angiogenesis by upregulation of EPOR, which amplifies the effect of EPO on activation of the VEGF/VEGFR2 and Ang1/Tie2 pathways. Our results provide the evidence for crosslink between TNF and EPOR to coordinate the onset of angiogenesis in cerebral endothelial cells.
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