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journal contribution
posted on 2019-03-04, 18:47 authored by Fariborz Soroush, Yuan Tang, Hasan M. Zaidi, Joel B. Sheffield, Mohammad F. Kiani
In the event of a radiologic catastrophe, endothelial cell and neutrophil dysfunction play important roles
in tissue injury.Clinically available therapeutics for radiation-induced vascular injury are largely supportive. PKCd
was identified as a critical regulator of the inflammatory response, and its inhibition was shown to protect critical
organs during sepsis. We used a novel biomimetic microfluidic assay (bMFA) to interrogate the role of PKCd in
radiation-induced neutrophil–endothelial cell interaction and endothelial cell function. HUVECs formed a complete
lumen in bMFA and were treated with 0.5, 2, or 5 Gy ionizing radiation (IR). At 24 h post-IR, the cells were
treatedwitha PKCd inhibitor for an additional 24h.Under physiologic shear flow, the role of PKCd on endothelium
function and neutrophil adherence/migration was determined. PKCd inhibition dramatically attenuated IRinduced
endothelium permeability increase and significantly decreased neutrophil migration across IR-treated
endothelial cells. Moreover, neutrophil adhesion to irradiated endothelial cells was significantly decreased after
PKCd inhibition in a flow-dependentmanner. PKCd inhibition downregulated IR-induced P-selectin, intercellular
adhesion molecule 1, and VCAM-1 but not E-selectin overexpression. PKCd is an important regulator of
neutrophil–endothelial cell interaction post-IR, and its inhibition can serve as a potential radiation medical


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