摘要

Background and purpose: This study aimed to characterize a link between X-linked inhibitor of apoptosis protein (XIAP) expression, apoptosis induction, Nuclear Factor kappa B (NF-kappa B) activity and the anti-inflammatory properties of low-dose ionising-radiation (LD-RT).
Material and methods: EA.hy.926 endothelial cells (ECs) were irradiated with doses ranging from 0.3 to 3 Gy, and subsequently stimulated by TNF-alpha, and XIAP expression was either detected by immunoblotting or TaqMan-PCR. Apoptosis was quantified by AnnexinV staining or by caspase 3/7 activity assays. NF-kappa B transcriptional activity was analysed by a luciferase reporter assay, secretion of Transforming Growth Factor beta 1 (TGF-beta(1)) and adhesion of peripheral blood mononuclear cells (PBMC) to EC were quantified using ELISA and adhesion assays.
Results: LD-RT of the activated EA.Hy.926 EC induces XIAP expression in a discontinuous manner with a relative maximum at 0.5 Gy and 3 Gy which parallels a discontinuity in apoptosis induction and caspase 3/7 activity. siRNA-mediated attenuation of XIAP resulted in an increased rate of apoptosis, a hampered NF-kappa B transcriptional activity and a diminished secretion of TGF-beta(1). As compared to control-siRNA treated cells, adhesion of PBMC to EC was increased in XIAP depleted EA.Hy.926 EC.
Conclusion: The modulation of apoptosis NF-kappa B activity and TGF-beta(1) by XIAP in irradiated and subsequent stimulated EC contributes to an impaired PBMC/EC adhesion and to the anti-inflammatory properties of LD-RT.

  • 出版日期2010-11